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Online Resumes with "adverse events"



Experienced Project / Safety Coordinator

To secure a challenging position in which my abilities and experience will be of value to an organization offering the opportunity for increased responsibility and knowledge.

Ideal Companies: Duke Univeristy, Merck & Co, Pfizer

Tags for this Online Resume: drug safety, clinical, research, coordinator

Clinical Research Professional

To obtain a position with a small or mid-size pharmaceutical company managing a one or more clinical development programs.

Tags for this Online Resume: clinical , safety , adverse events, efficacy , clinical data , trial management

Agricultural Technician

Tags for this Online Resume: Drug Safety Associate , Serious Adverse Event , Argus , Safety reviewer, MedWatch , CIOMS

Clinical Research Coordinator

To manage clinical trials in a CRO environment.

Tags for this Online Resume: Research Coordination, Data Management, EDC experience, Regulatory, Adverse Events, Clinical Trial

Baggage Porter

Tags for this Online Resume: adverse event, MedDRA, nurse, WHO dictionary, medical

Featured Profile

Clinical Research Associate

SUMMARY OF QUALIFICATIONS • Foreign graduate Medical Doctor and licensed RN with more than 22 years of clinical and research experience. US citizen. Fluent in English, Russian and Romanian • Extensive training in Good Clinical Practices, ICH Guidelines, SOPs through various Sponsors • In depth therapeutic and protocol knowledge as per Sponsor’s assignment. Excellent organizational and problem-solving skills.

Ideal Companies: Biotech companies

Tags for this Online Resume: research associate, biotech, CRA, Las Vegas, pharmaceutical, health

Featured Profile

Featured Profile

Registered Nurse - Drug Safety Associate,Coder, Product Surveillance/Product Safety

I am seeking for a stable and well established company that is growing. Also,what I am looking for in a new job is for employers that care about their employees and acknowleges them for their good hard work. I would also hope that good training is provided so that the individual such as myself can be productive for the company and contribute towards it's success rate. I would also hope that it was a warm welcoming environm...

Ideal Companies: Cephalon Pharmaceutical, Teva Pharmaceutical, Azur Pharmaceutical, GlaxoSmithKline, United BioSource

Tags for this Online Resume: Registered Nurse, Drug Safety Associate, Coder, Safety Surveillance, Adverse Event Coordinator

Clinical Research Associate, seeking entry-level, in-house opportunity

I am an excellent candidate for a Clinical Research Associate position due to my unique combination of experience in Preclinical Research and Development, Pharmaceutical Sales, and CRA Training. In addition to the skills and accomplishments detailed in my c.v., please consider the following highlights: Certification from Barnett International (July 2012): 10-Week CRA & CRC Beginner Program. Coursework emphasized FDA reg...

Featured Profile

Healthcare information specialist

Healthcare information professional with over 20 years experience working in the pharmaceutical industry looking for new career opportunity in sales, customer service, information services, etc. I have experience answering time-sensitive requests from both Medical R&D issues related to due diligence, adverse event reporting, FDA drug safety response letters and regulatory submissions, as well as the commercial side of Mark...

Clinical Research Associate

Highly motivated and experienced biomedical professional with expert knowledge and proficiency in clinical research monitoring. A certified CRA. Hands-on experience in the clinical investigations of novel pharmacological products. Eager to translate expertise gained in research and monitoring to measurable success in the field clinical studies. A demonstrated record of academic achievement and recognition, accompanied by e...

Tags for this Online Resume: Clinical Site Monitoring , Identification and interviewing of potential investigators, ICH GCP Training , Adverse Event Reporting, Study Planning Activities