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Title |
Location - (Distance) |
Salary/Rate |
Date |
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clinical research associate |
Jersey City, NJ US - ( mi.) |
$40K to $50K |
Jul 12 |
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| OBJECTIVE A position in which my knowledge of pharmaceutical science and managerial skills can be utilized EXPERIENCE PHARMACY INTERN, Torrent Pharmaceutical Ltd., Gujarat, India Summer • Participated in manufacturing process of tablets and capsule starting from mixing of ingredients to finished products as per US Pharmacopoeial standards • Knowledgeable of SUPAC guidelines and collection of data required for chemistry, manufacturing and control(CMC) as a part of ANDA submissions and ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | Post Graduate Degree |
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REGULATORY AFFAIRS |
New Hope, PA US - ( mi.) |
$120K to $130K |
Jul 30 |
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| . Web Site: http://www.TonySGreen.com Tony Green, PhD OBJECTIVE: To find a challenging position in Pharmaceutical Regulatory Affairs. Web Site with Full Details of Employment History: http://www.TonySGreen.com SUMMARY: A Regulatory Affairs specialist with an in-depth understanding of, and proven successes, in drug development in a global environment. Recent Positions held: Green & Associates: Feb -present Valeant http://www.valeant.com/ Tibotec Inc: May - Feb J&J PRD: June – ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | 4-Year College Degree |
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Regulatory Affairs |
San Diego, CA US - ( mi.) |
Negotiable depending on position |
Mar 30 |
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| Objective: To obtain a challenging and rewarding position in a stable environment, where I can continue to enhance my regulatory skills and grow with a company that will sustain over time. Profile Summary: A hard working, dedicated self starter with more than years of combined experience in the regulatory/clinical research/pharmaceutical/medical device/biotechnology industry. Having a bachelor’s degree in Health Science, combined with my extensive training in related industries and my ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | 4-Year College Degree |
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Regulatory Affairs |
Fort Lauderdale, FL US - ( mi.) |
$40K to $60K |
Jun 27 |
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| QUALIFICATION SUMMARY o Confidence conducting detailed research using library and Internet resources. o Research, Data collection, trend analysis experiences o Writing skills developed via practical experiences, as well as academic papers and research projects o Windows Applications, Microsoft Word, Excel, PowerPoint, and Internet Utilities o Project management, time management, writing and oral communications skills gained from employment, education, and other activities o Skills, interests, ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | 4-Year College Degree |
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Internship in Regulatory Affairs/Quality Control/ Clinical Trials |
Los Angeles, CA US - ( mi.) |
Along with Good Benefits |
Dec 29 |
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| Education: University of Southern California, Los Angeles, CA GPA . MS in Biomedical Engineering Dec Institute of Engineering & Technology, India GPA . Bachelor of Technology in Biotechnology May Relevant Courses: • Quality Systems & Standards • Six-Sigma Quality Resources for Health Care • Quality Management for Engineers • Engineering Project Management • Regulation of Medical Devices & Diagnostics • Global Regulation of Medical Products • Structure and Management of Clinical ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | Post Graduate Degree |
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Regulatory Affairs Manager |
Havertown, PA US - ( mi.) |
65,000 > |
Aug 27 |
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| SUMMARY Over years of pharmaceutical industry experience working in Clinical Data Management, U.S. Regulatory Affairs and International Regulatory Affairs. Regulatory representative on interdisciplinary project teams to support worldwide registration of prescription and over-the-counter products. EXPERIENCE WYETH-AYERST RESEARCH, ST. DAVIDS, PA Worldwide Regulatory Affairs, Senior Coordinator September – Present Assist in the development of effective, proactive regulatory strategies on ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | 4-Year College Degree |
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Clinical Research Associate |
Fort Wayne, IN US - ( mi.) |
$40K to $60K |
Oct 27 |
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| Objective Seeking CRA opportunity in regulatory affairs or post market. Experience Analyst -present Baker & Daniels, Fort Wayne, IN „Xsupport of software/hardware/netware fr three satellite offices presentation preparation for legal staff „Xproject management for satellite offices Contract Technician/Administrator - Medical Group, Fort Wayne, IN „Xinstall of billing servers and workstations „Xeducate medical personnel to new technology „Xmaintain software/hardware/netware ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | 4-Year College Degree |
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Regulatory Affairs Associate |
boston, MA US - ( mi.) |
open $10K |
Jul 26 |
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| OBJECTIVE: Looking for an associate position to develop essential skills and gain experience in the areas of Regulatory Affairs and Quality Assurance of drugs, medical devices and biological products. EDUCATION: Northeastern University, Boston, MA [-present] Master of Science in Regulatory Affairs for Drugs, Biologics and Medical Devices [GPA: ./] Relevant courses Drug and Medical Device Regulations New Drug Development Practical aspects of Regulatory Compliance European Union ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | Post Graduate Degree |
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Clinical Research |
Alpharetta, GA US - ( mi.) |
$60K to $200K |
Nov 5 |
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| JEANNIE-MARIE SKINNER Results-oriented professional with twenty years of experience in the global pharmaceutical industry including Regulatory Affairs, Clinical Research, Project Management and Licensing and Acquisitions. Successful interactions with FDA including NDA approvals, labeling negotiations, end of phase II meetings and pre-approval inspections. An innovative and committed participant on global drug development team. PROFESSIONAL EXPERIENCE RIVER’S EDGE PHARMACEUTCALS, LLC – SUWANEE, ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | Post Graduate Degree |
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Clinical/Regulatory Assistant |
Smyrna, GA US - ( mi.) |
$50K to $70K |
Nov 13 |
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| Professional Summary I am having years of Pharmaceutical Industry experience in the fields of Drug Regulatory Affairs and Formulation Research and Development. Extensive regulatory experience in the dossier preparation (CMC) for Asia Pacific countries, maintenance of regulatory database & preparation of product master files. Academic Profile Master of Pharmacy (Pharmaceutical Science) Panjab University, Chandigarh, India Bachelor of Pharmacy Panjab University, Chandigarh, India Experience ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | 4-Year College Degree |
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Clinical Research Coordinator |
Richmond, CA US - ( mi.) |
Negotiable $50K to $100K |
Feb 5 |
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| EDUCATION Georgetown University, Washington, D.C • M.S Pharmacology Graduated: May, James Madison University, Harrisonburg, VA • B.S. Biology Graduated: May, RELEVANT EXPERIENCE ClinProxy Research Services Regional Clinical Research Associate (Intern) June - Present • Phase II (a) sequential, dosing, double blind, randomized, placebo controlled, multi-center clinical study of efficacy and safety of PROLIPOSTAT® as preventive treatment of cognitive dysfunction as a complication of ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | Post Graduate Degree |
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Entry Level Regulatory Affairs |
Boston, MA US - ( mi.) |
$50K to $90K |
Jul 14 |
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| OBJECTIVE: Looking for an opportunity in a reputed organization, which will help me deliver my best and upgrade my skills in the field of regulatory affairs and meet the demands of the organization. WORK EXPERIENCE: ) MedXview Inc. April - Present Position: Intern, Regulatory Affairs • Well versed on eCTD software ‘eCentral’. • Assisting supervisor in region specific electronic submission. • Assisting supervisor through working with clients to compile, monitor, track, validate, and ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | Post Graduate Degree |
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Regulatory Affairs |
Nashville, TN US - ( mi.) |
$60K to $70K |
Jan 3 |
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| SUMMARY: Over years of experience in the clinical research industry, with focused experience in Regulatory Affairs. Solid experience managing, mentoring, and training employees in regulatory affairs. Dedicated to providing top-of-the-line customer service to both internal and external customers, including government agencies. Extensive experience in regulatory submissions, site initiation requirements, ICH/GCP requirements, and the development of strategic regulatory pathways. Adept at ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | 4-Year College Degree |
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Clinical Research Associate |
Walnut, CA US - ( mi.) |
$50K to $60K |
Mar 1 |
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| OBJECTIVE Self- motivated, well-qualified professional seeking a challenging career in the area of Clinical Research SUMMARY •Excellent capacity to multitask and manage numerous, often competing priorities with ease while delivering superior results •Demonstrated ability to work and communicate effectively in cross functional teams •Experience in development of clinical and regulatory strategy •Worked previously in a GLP regulated environment •Strong background in Immunology and Microbiology ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | Post Graduate Degree |
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Manager, Regulaltory Affairs |
Pacifica, CA US - ( mi.) |
$100K |
Mar 7 |
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| REGULATORY AFFAIRS – REGULATORY OPERATIONS – CLINICAL REGULATORY SUMMARY Over years Pharmaceutical and Biotechnical Experience Regulatory Affairs, Regulatory Operations and Clinical Regulatory Affairs New Drug Applications, Investigational New Drug Applications, Clinical Trial Applications Marketing Authorization Applications and Dossier Preparation PROFESSIONAL HISTORY Regulatory Affairs Consultant – Current Primary Consultant in Regulatory Affairs and Clinical Regulatory activities to ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | 4-Year College Degree |
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Regulatory Affairs Associate |
- ( mi.) |
$40K to $50K |
Feb 2 |
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| ; Meticulously completes tasks while being able to multi-task in a fast-paced environment Familiarized with the Food & Drugs Act/Regulations, and relevant guidance documents Knowledge of pre-clinical, clinical, and post-marketing phases of drug development Clear understanding of general submission requirements for NDS, SNDS, and CTA Proficient in Microsoft Office & Adobe; good typing skills and computer knowledge Great at organizing, planning, and problem solving individually or as a part of a ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | Post Graduate Degree |
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Regulatory Affairs Specialist/Associate |
San Diego, CA US - ( mi.) |
$70K to $100K |
Sep 16 |
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| Kim L. Bloom Matinal Circle, San Diego, CA H: -- C: -- * Email: Objective: To obtain a challenging and rewarding position in a stable environment, where I can continue to enhance my regulatory skills and grow with the company that will sustain over time. Profile Summary: A hard working, dedicated self starter with more than years of combined experience in the regulatory/clinical research/pharmaceutical/medical device/biotechnology ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | 4-Year College Degree |
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Regulatory Affairs Specialist |
Rockaway, NJ US - ( mi.) |
$70K to $80K |
Jun 18 |
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| Yuko S. Hartley Deer Run Rockaway, NJ -- (H) -- (Cell) Email: EDUCATION: - Rutgers University, New Brunswick, NJ Bachelor of Science, Bio-resource Engineering - University of Illinois, Champaign-Urbana, IL Master of Social Work - Musashi University, Tokyo, Japan Bachelor of Arts, British and American Culture CERTIFICATE: E.I.T.(Engineer-In-Training) Certificate, PROFESSIONAL AFFILIATION: Regulatory Affairs ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | Post Graduate Degree |
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Regulatory Affairs Associate |
Los Angeles, CA US - ( mi.) |
$40K to $70K |
Mar 24 |
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| Saumil Rajendra Shah West th Street, Apt No., Los Angeles, CA Tel: -- Email: EDUCATION University of Southern California, Los Angeles, CA December Master of Science, Biomedical Engineering GPA: . Mumbai University, Mumbai, India May Bachelor of Engineering Biomedical Engineering GPA: . Relevant Coursework • Regulation of Medical Devices and Diagnostics: (k), PMA, IDE Applications, Biocompatibility (ISO ), Post-market ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | 4-Year College Degree |
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Regulatory Affairs Associate |
Oakville, ON CA - ( mi.) |
$40K to $50K |
Jun 19 |
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| S T R E N G T H S • Strong computer skills including creating PDF documents with Adobe Acrobat and strong proficiency with applications such as MS: Word, Excel, Access, PowerPoint, and Project • Responsible individual with excellent time management skills through the prioritization of tasks • Motivated, ambitious and enjoys challenges, dedicated to the task at hand • Dedicated team player; self-directed learner; strong attention to detail S K I L L S • Knowledge and skills for preparing and ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | Post Graduate Degree |
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Regulatory Affairs |
Los Angeles, CA US - ( mi.) |
$50K to $60K |
Feb 1 |
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| OBJECTIVE Seeking the role of a regulatory person, to further my knowledge with the aim of attaining doctrinaire perfection required to excel in this field while playing a key role in contributing to the growth of the company. EDUCATION University of Southern California, Los Angeles CA Jan ‘-Dec’ Masters in Pharmaceutical Sciences [GPA: .] University of Mumbai, Mumbai Education Trust Institute of Pharmacy (MET) May Bachelor of Pharmacy [GPA: .] CERTIFICATIONS • HIPAA Privacy ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | Post Graduate Degree |
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Clinical Research Assistant, Regulatory Affairs Assistant |
Mercer Island, WA US - ( mi.) |
I am also willing to intern for up to three months. |
Apr 5 |
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| OBJECTIVE Apply my life science education along with my communication, organizational and project management skills to transition into a career in Clinical and Regulatory Affairs. EXPERIENCE /-Present Kriger Research Group International, Austin, Texas Clinical Research Associate Program Intern Studied the design and contents of CRFs, study protocols, SOPs, and other clinical trial documents including Site Monitoring Reports and SAE Report Forms. Started clinical study tasks on simulated ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | Post Graduate Degree |
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Regulatory Affairs Manager |
Ballwin, MO US - ( mi.) |
$60K to $120K |
Feb 2 |
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| BELA CHAUHAN Ridgetree Trails Drive Wildwood, MO Tel. () - Carrier Objective: I am looking for a position in regulatory affairs, where I can utilize my unique skill set of regulatory compliance in addition to my experience in immunology. With increasingly successful use of biological drugs, the function of a regulatory specialist also demands understanding of the underlying mechanism of drug interaction through scientific knowledge. With my firsthand ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | Post Graduate Degree |
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Regulatory Affairs Associate |
Long Beach, NY US - ( mi.) |
$40K to $60K |
Sep 12 |
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| OBJECTIVE To obtain a suitable position in Regulatory Affairs in the Pharmaceutical Industry. RELEVANT EXPERIENCE Genpharm Inc., Toronto, Canada A leading manufacturer of generic pharmaceuticals Regulatory Affairs Associate November – November · Prepared and submitted regulatory documents such as Clinical Trial Applications (CTA), Abbreviated New Drug Applications (ANDA), Supplements, Amendments, Drug Listing of approved products and Annual reports to FDA and Health Canada. · ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | 4-Year College Degree |
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Regulatory Affairs Specialist |
San Diego, CA US - ( mi.) |
flexible depending on position description |
Jul 30 |
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| Kim L. Bloom Matinal Circle San Diego, CA home/Mobile Email: Profile Summary: A motivated, hard working, dedicated, self-starter with more than years of combined experience in the regulatory/clinical research/drug safety/pharma/medical device/biotechnology industry. Having a Bachelor of Science degree in Health Science combined with my extensive training in related industries and my passion for patient health and safety has enabled me ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | 4-Year College Degree |
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Manager, Specialist |
Yonkers, NY US - ( mi.) |
Salary negotiable according to commute |
Jul 22 |
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| EXPERIENCE: Delcath Systems, Inc. (Drug/Devices) / – // Manager, Regulatory Affairs (Consultant) Oversee regulatory and clinical affairs in all aspects In charge of all submissions: IND/IDE—Adverse Events, Protocols, Annual report, Amendments, Meeting packages review, Draft response to FDA Contact for CDER AND CDHR Advisor on Pre-clinical studies Develop and help other consultants develop reports for meeting preparation with FDA Review all Adverse Events Review labels for devices ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | Post Graduate Degree |
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Regulatory Affairs Specialist |
Philadelphia, PA US - ( mi.) |
$80K to $100K |
Jun 18 |
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| Twenty plus years of increasing employment responsibilities. Expertise includes in-depth knowledge of and support of pharmaceutical product registrations. Strengths include: strict attention to detail and accuracy; excellent interpersonal and organizational skills, maintaining effective working relationships with other clinical and regulatory groups; demonstrated ability “to get the job done� within challenging time constraints. Adept at handling varied high-priority tasks for ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | 4-Year College Degree |
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CMC Specialist |
Philadelphia, PA US - ( mi.) |
$80K to $90K |
Mar 19 |
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| CMC Data Analyst - Regulatory Affairs Coordinator, qualified by education, training and work experience. Over the years my work has spanned a variety of therapeutic areas for both in-line and OTC products for human use. I have worked as an international and domestic regulatory coordinator acquiring knowledge of and adherence to the domestic and global regulatory requirements for agencies including the FDA, Health Canada, ICH and EMEA. Strengths include: strict attention to detail and accuracy; ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | Post Graduate Degree |
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regulatory affairs associate |
Jamaica, NY US - ( mi.) |
$50K to $60K |
Jul 1 |
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| Vaishali B. Patel Address: - th Drive Apt # A, Jamaica NY – Phone: -- (cell). Email: vaishali b .in OBJECTIVE To obtain a position that allows me to utilize my skills and constantly acquire in-depth knowledge in the Regulatory Affair field thereby adding to my personal as well as organization’s growth. EDUCATION M.S. / Drug Regulatory Affair / Long Island University, Brooklyn, NY. Jan – May. GPA . B.S. / Pharmacy / Bombay University, India. May ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | 4-Year College Degree |
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Regulatory Affairs associate |
North York, ON CA - ( mi.) |
$30K to $40K |
Jul 4 |
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| .com Highlights of Qualifications • + years of experience working in Regulatory Affairs departments. • Knowledge of making application files of registration in international regions. • Excellent attention to details, verbal and written communication skills, organizational skills, planning skills, analytical skills, strong inter-personal skills, time management skills, negotiation skills and multi-tasking ability • Experience of working in coordination with quality assurance, quality control, ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | 4-Year College Degree |
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Project Manager |
Ellicott City, MD US - ( mi.) |
$60K to $110K |
Feb 13 |
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| Li-Hong Paul Yeh, Ph. D. Curriculum Vitae Address: Jay Drive Ellicott City, MD - Citizenship: USA Education: Ph.D. University of Missouri, Columbia, MO December (Chemical Engineering) M.S. University of Missouri, Columbia, MO December (Chemical Engineering) B.S. National Cheng Kung University, Taiwan, June (Chemical Engineering) Additional training: Therapeutics Biotech Updates for Pharmaceutical Inspector Training Team Biologics ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | 4-Year College Degree |
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Clinical research Associate |
Wake Forest, NC US - ( mi.) |
$40K to $50K |
Nov 28 |
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| SUMMARY: A self-motivated professional with ten years of relevant management and business experience, I also enjoy working independently or as a team. Particularly interested in pursuing a career in Clinical Research and Regulatory Affairs in the Pharmaceutical Industry. Committed to being a lifelong learner taking seminars and classes to enhance my knowledge and expertise within the pharmaceutical, CMC, clinical trials, regulatory affairs, and compliance. I am highly energetic and enjoy ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | 4-Year College Degree |
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Research Scientist/regulatory Affairs |
Richboro, PA US - ( mi.) |
$40K to $80K |
Mar 8 |
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| SUMMARY Research Scientist/Regulatory Affairs with extensive expertise in Drug Discovery in the Pharmaceutical Industry and in a hospital clinical environment. Strong knowledge of FDA regulations, GCP compliance and medical terminology. A highly motivated team player with excellent problem solving skills and a demonstrated ability to work effectively across all levels of management. Able to learn new techniques quickly and to effectively train others. Familiar with all aspects of IND, NDA, and ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | 4-Year College Degree |
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Executive Associate |
San Mateo, CA US - ( mi.) |
Annual Bonus, Company Profitability |
Dec 7 |
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| Objective A challenging position in which to utilize my experience in the biotechnology industry, apply my legal knowledge and leverage my education in biological sciences. Executive Summary • Over years of work experience in biotechnology companies • Familiar with corporate legal environment and proficient in both US and foreign patent preparation and prosecution support • Excellent organization and multitasking skills • Versatile and adaptable; effective as team member or independently • ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | 4-Year College Degree |
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research associate, study co-ordinator |
new delhi, new delhi IN - ( mi.) |
$10K |
Sep 15 |
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| Objective To work in the field of Pharmaceutical Sciences for utilization and enhancement of my Professional knowledge. Professional Attributes I am a Pharma Professional who enjoys taking initiative. I am highly responsible, self-directed, hard working and creative person. I am quick to grasp new ideas and willing to be part of a dedicated team. Educational Qualifications M. Pharm (Pharmacology), Result awaited, Jamia Hamdard, New Delhi-. B. Pharm, st Div. from Jamia Hamdard, New Delhi. ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | Post Graduate Degree |
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Clinical Research Manager |
Allentown, PA US - ( mi.) |
$70K to $100K |
Apr 14 |
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| .D. OBJECTIVE To obtain a position within the Pharmaceutical Industry where my many years of experience in Clinical Research, Regulatory Affairs, Medical Affairs and Business Development, can be fully utilized. RELEVANT EXPERIENCE MEDICAL AFFAIRS Responsible for the clinical research, regulatory affairs, and training of personnel for the development of new products. CLINICAL RESEARCH: Main Therapeutic Areas : Neurology-Oncology-Growth-Fertility-Osteoporosis- REGULATORY AFFAIRS: Compiled a ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | Post Graduate Degree |
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Clinical Studies |
Hialeah, FL US - ( mi.) |
Open for discussion |
Mar 22 |
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| CLINICAL TRIALS EXECUTIVE –IMPLEMENT MANAGEMENT OF CLINICAL PROJECTS PROJECT TEAM TIMELINES-BUDGETS-QUALITY PHYSICIAN NETWORK DEVELOPMENT- LEADERSHIP DECISIONS AND PROJECT DELIVERY- STRATEGY PLANNING STANDARD OPERATIONAL PROCEDURES (SOP’s) DRAFT-IMPLEMENTATION-MONITOR FDA COMPLIANCE AND EMEA GUIDELINES AND SUBMISSIONS MEDICAL PRODUCT SAFETY COMPLIANCE- PHARMACOVIGILANCE PDUFA- DATABASE DEVELOPMENT-IMPLEMENTATION-MANAGEMENT SELECTED ACHIEVEMENTS: · Implement PDUFA- in the post marketing ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | 4-Year College Degree |
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Clinical Regulatory Affairs |
São Paulo, SP BR - ( mi.) |
$20K to $30K |
Jul 24 |
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| EDUCATION -Post graduation in Clinical Pharmacology, December, Faculdades Oswaldo Cruz, Sao Paulo, SP, Brazil -Post graduation in Clinical Research, November, Faculdade de Ciencias Medicas da Santa Casa, Sao Paulo, SP, Brazil -Psychology, December, Universidade Estadual Paulista- UNESP, Bauru, SP, Brazil EMPLOYMENT -PRA International Sao Paulo, Brazil Unblinded Clinical Research Associate May, to present Conduction of Drug Monitoring Visits Assist with query resolution ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | Post Graduate Degree |
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clinical research |
ahmedabad, gujarat IN - ( mi.) |
10000 inr |
Jan 30 |
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| RESUME Name: Nishith Harshadkumar Sheth , Ishwarcharan App, Nr. Fortune Landmark Hotel, Behind Azad sweet, Usmanpura, Ahmedabad- Gujarat, India, Ph: - Email: Career objective: To work in an open, exciting and professional environment having excellent growth prospects. Also looking for creative, prosperous, enlighten & respectful organization to join where I can gain knowledge, develop my skills and push the organization on the peak of the market. Also ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | Post Graduate Degree |
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Clinical Research |
Mississauga, ON CA - ( mi.) |
$40K to $60K |
Sep 17 |
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| independent and motivated professional looking to obtain a position within the Pharmaceutical industry that fully utilizes my strong research, organization, communication skill sets and ability to work cross functionally to achieve deadlines. PROFESSIONAL EMPLOYMENT EXPERIENCE MDS Pharma Services Clinical Trials Project Management Project Coordinator – Present · Integral to the initiation and successful monitoring of investigational sites through communication and coordination of ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | 4-Year College Degree |
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Regulatory Affairs/Quality Assurance/Clinical Research Associate/Instructor |
Harwinton, CT US - ( mi.) |
$50K to $70K |
Jun 1 |
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| University of Connecticut, Storrs, CT Bachelor of Science, School of Liberal Arts and Sciences, May Major: Molecular and Cellular Biology GPA: ./.Research and Relevant Experience CuraGen Corporation, Branford, CT Quality Assurance Specialist (Full Time Intern) – Duration: Months• Conducted Audits to ensure the company was following the proper standard operating procedures (SOPs) and compliance with current Good Manufacturing Practices (cGMPs) set by the FDA. Supervisor: Dr. Hans ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | Post Graduate Degree |
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clinical pharmacologist/pharmacokineticist |
Gaithersburg, MD US - ( mi.) |
consulting rates $150 per hour |
May 12 |
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| -mail PROFESSIONAL EXPERIENCE BioPharm Global, Inc. Gaithersburg, MD Consultant April -Present Founded BioPharm Global Inc., a consulting firm specializing in pharmaceutical development, clinical development programs and regulatory submissions. Services are focused and tailored to meet the needs of clients in a highly cost effective manner. Involvement in approved New Drug Applications (NDA) has included Carbatrol® (), Adderall XR® (), Equetrol® (), ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | Post Graduate Degree |
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Clinical / Regulatory Affairs |
Euless, TX US - ( mi.) |
$60K to $80K |
Nov 11 |
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| NANCY UNDERWOOD Bay Avenue Phone: -- Euless, Texas SUMMARY OF QUALIFICATIONS Experienced pharmaceutical professional proficient in post marketing regulatory reporting of OTC products to FDA. • Well versed in FDA regulations regarding adverse event reporting of OTC products. • Knowledgeable in preparation of NDA submissions. • Adept in validation of electronic computer systems. • Quick learner of new computer systems with rapid familiarization ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | 4-Year College Degree |
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Manager Medical and Regulatory Affairs |
Thane IN - ( mi.) |
$110K to $175K |
Aug 9 |
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| bjectiveTo achieve a global managerial position, bringing out the application of my knowledge and experience leading to mine as well as the organizational growth.Industry experienceManager- Medical and Regulatory services; UCB-Pharma, India; // – to date Key Achievements • Analyzed the raw data of XYZAL In Clinic Experience (X-ICE), a post marketing surveillance of patient feedback on safety and efficacy of XYZAL with the help of statistician. Compiled XICE in form of articles for ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | Post Graduate Degree |
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regulatory affairs manager/Senior Specialist |
Philadelphia, PA US - ( mi.) |
$70K to $80K |
Dec 12 |
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| PROFILEI am a seasoned health science professional who combines a biomedical research background, regulatory affairs and clinical trials experience, and medical writing expertise with the superior ability to foster interpersonal and team dynamics. My integrity, as well as my communication and relationship-building skills, generally allow me to quickly gain the trust and respect of my colleagues. I have over years experience and technical expertise in the creation/submission of regulatory ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | Post Graduate Degree |
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Scientist |
- ( mi.) |
$40K to $70K |
Mar 19 |
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| Well-organized professional with over years experience in the pharmaceutical industry seeks a position using my strong interpersonal and communication skills and ability to focus on details. SUMMARY • Authored technical reports, manuscripts, and synthesis summaries used in IND and NDA submissions. • Working knowledge of pharmaceutical regulatory requirements including: ISO , OSHA, GLPs and GMPs, including SOPs. • Strong communication skills which include organization, preparation, and ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | Post Graduate Degree |
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Clinical Research |
Cincinnati, OH US - ( mi.) |
$50K to $80K |
Apr 13 |
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| SUMMARY: Results-driven and quality-minded clinical research professional with + years of diversified experience in an academic setting with proven success in managing a large number of projects and individuals with varying educational backgrounds. Consistently recognized for strengths in communication, collaboration and leadership of successful research teams, I look forward to combining my biology/chemistry background and clinical skills to explore further scientific development ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | 4-Year College Degree |
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MEDICAL SCIENTIST LIAISON, CLINICAL RESEARCH, REGULATORY AFFAIRS |
ROUND ROCK, TX US - ( mi.) |
$90K to $120K |
Dec 12 |
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| EDUCATION- CLINICAL RESEARCH FELLOWSHIPUniversity of Texas Health Science Center School of MedicineHouston, TX- MEDICAL DEGREEUniversidad Autonoma de TamaulipasSchool of MedicineMexico PROFESSIONAL EXPERIENCEMarch -Present: CLINICAL RESEARCH & REGULATORY AFFAIRS University of Texas Health Science Center Ophthalmology Houston, TX Director: Richard G. Urso, M.D.Primary responsibilities:• Good Clinical Practices• Manages protocol development, study conduct and data ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | Post Graduate Degree |
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Senior Production Tech, Fermentation |
Sacramento, CA US - ( mi.) |
$40K to $60K |
Dec 13 |
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| William Uwoghiren Objective: Clinical Research Associate Employment Bayer HealthCare Berkeley, California Senior Production Tech Fermentation / to Present ?Operate and monitoring of fermenter through computer distribution control system (DCS) for the production of recombinant factor VIII, and in eighteen months was promoted from entry level to a senior Tech. ?Prepare media solution, and operate cell separation and ultra filtration skid. Document all operation in strict compliance with cGMP, ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | Post Graduate Degree |
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Clinical Research Associate/Regulatory Affair/Product Specialist |
Kuantan, Pahang MY - ( mi.) |
$20K to $70K |
Jul 18 |
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| University of Leeds (UK) MSc Bioscience (Human Genetics) with Merit. Dissertation Title: mtDNA analysis of Fiji Islands to investigate the settlement of Fiji as a stepping stone from Melanesia to Polynesia. - Working and travelling aboard. - University of Malaya (Malaysia) BSc (Hons)Bioinformatics (:). Final Year Research Project: Evolutionary trace analysis on metalloenzyme active site (Methane Monooxygenase) - STPM, Sekolah Menengah Kebangsaan Abdul Rahman Talib ... More |
| Career Focus: | VALUE NOT FOUND |
Education Level: | Post Graduate Degree |
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