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Online Resumes with "Adverse Event Reporting"



Health care

Ideal Companies: Clif bar, Monster

Clinical Research Coordinator

Profile: Certified Clinical Research Associate professional with extensive recent focus in CVS research and clinical trials. Combine resourcefulness and problem solving skills with clinical knowledge to consistently deliver improved research and production results. Team player dedicated to quality, continuous improvement and bottom-line objectives. QUALIFICATION HIGHLIGHTS • Knowledgeable in all areas of research including...

Ideal Companies: quintiles, Pfizer, Novartis, Aerotek, Abbott, J&J, Merck

Tags for this Online Resume: CRA program, clinical research coordinator

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

Highly Experienced, Deidicated, Ethical, Compassionate Medical Professional with Diversified Background.

I am looking for a position working with clients with varying levels of medical attention. I am looking to Supervise and train medical staff to develop a team of consistant, high quality, cohesive team members who enjoy what they do. I am a skilled professional medical assistant, office supervisor with several years experience training, managing and hiring medical team members with a focus on developing a staff with indiv...

Ideal Companies: Hospitals, Private Physician Offices, Walk-In edical Centers

Tags for this Online Resume: Supervisor, Phlebotomist, Customer Service, Medical Assistant, Team Development, File Manager, Adverse Event Reporting, Office Inventory Control, Team Facilitator, Office Manager, Medical Office Manager, Patient Focused, Microsoft Office Proficient, Highly Able to learn new systems

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

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

Drug Safety / Pharmacovigilance - RTP, NC

Dynamic, enthusiastic, and performance-driven Doctor of veterinary medicine intent on transferring 10 years of knowledge and experience in a clinical setting to a challenging career working in the Pharmaceutical or Contract Research Organization industry with a progressive company offering opportunities for growth and advancement. Outstanding team player and communicator with highly detailed documentation skills seeking t...

Tags for this Online Resume: Medical terminology, ICH/GCP guidelines, DIsease states, Pharmacology, Customer service, Medical writing