CV, Curriculum Vitae and Online Resumes Search

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Online Resumes with "postmarketing"

Executive in the pharmaceutical and biotechnology areas

I am an executive with 25-years experience and a demonstrated success in pharmaceutical and biotechnology drug development, drug discovery and delivery of conventional drugs, proteins, and peptides; I am well-versed in regulatory requirements and interactions with the FDA and other regulatory agencies. As a PI on NIH funded projects, I conducted Phase 1 and Phase 2 clinical studies in mucositis, severe sepsis and nosocomial...

Tags for this Online Resume: program leader, project leader, consultant, preclinical, drug characterization, assay validation

Sr. Clinical research Associate/ Director of clinical research

Can undertake most of the tasks and works independently. Very much focussed on the timelines and quite goal tending. Willing to help others in their prioritized tasks. Excellent planning, design and implementation. Highly experienced in writing reports and data analyses.

Ideal Companies: Pharmaceutical industries, Biotech companies, Research institutes, hospitals and for profit mid to large companies.

Tags for this Online Resume: Director of clinical research, Manager of drug safety, Senior clinical research associate, Regional clinical research associate

Senior Pharmacovigilance Specialist with unique background

I am looking to bring my very unique background to a company that considers the areas of drug safety, risk management, and signal detection as an proactive opportunity to play significant roles in the life cycle of a product versus a regulatory necessity.

Ideal Companies: I am looking for a small to intermediate company that rewards creativity and hard work.

Tags for this Online Resume: Clinical and postmarketed products, Microsoft Office, Senior or management experience, All major safety datanases

Pharmacovigilance, San Antonio, Tx

Bring my expertise in pharmacovigilance and regulatory complaince for pharceutical or medical device products.

Tags for this Online Resume: Registered Nurse, Postmarketing Safety, Medical Device Reporting, pharmaceutical safety, pharmacovigilance, FDA compliance

Senior Safety and Pharmacovigilance Specialist

Seeking position with great potential for growth.

Tags for this Online Resume: Safety, Pharmacovigilance, FDA, ICH, IND, Postmarketing

Clinical Trials Professional

Desire to contribute in oversight of medical surveillance resourcing and performance quality for clinical trials transcending Phase II proof of concept to post-marketing evaluation.

Executive leader focused on rapid market growth and increasing profits by motivating and directing worldwide cross-functional teams to deliver innovation on-time, within budget, exceeding customer and quality expectations, while meeting all regulatory req

Twenty years of medical device/pharmaceutical experience including all aspects R&D, Engineering, Operations, Marketing and Quality for launching new products. This includes every stage of the product life cycle from customer requirements, risk management, feasibility, development, quality systems, design verification, pilot manufacturing, validations, regulatory approvals, clinical field testing, full manufacturing, produc...

Director, medical affairs

Tags for this Online Resume: medical affairs, medical information, clinical research, postmarketing surveillance, medical communications, medical science liaison

PharmD with drug safety, pharmacoviglance, medical information

drug safety/pharmacovigilance, medical science liason, medical information, associate director risk management

Ideal Companies: Pharmaceutical, Biotech

Tags for this Online Resume: argus, arisG, caviar, NWAES, MedDRA, Oracle AERS, argus, clintrace

Medical Affairs, Regulatory Affairs Associate, Clinical Affairs

Doctor of Medicine recognized with clinical trial expertise in medical device, drug safety, regulatory affairs, and post-market monitoring. Strong emphasis on utilization of cross-functional skills to advance medical systems and develop process improvements. Results-driven collaborator with effective oral and written communication and presentation skills. Patient advocate and contributor to public health awareness and educa...

Tags for this Online Resume: FDA MedWatch 21 CFR 820 803, Medical Device Class III, ICD, VT / VF, Medical Affairs, Regulatory Affairs, Drug Safety, Quality Assurance and Management, Public Health, Patient Relations, Medical Communication, SAP, Excel