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Online Resumes with "adverse events"



Featured Profile

Pharmaceutical Deputy Compliance/Internal Auditor/Governance/Risk Management/Internal Controls/Change Management

I am interested in a position where I can leverage the skills and experience I have gained over a career in the pharmaceutical industry.I am a skilled professional with over 15 years experience in compliance, risk management, corporate governance and change management, as well as R&D internal audit and assurance. I am an excellent communicator, with well-developed speaking and writing skills and in-depth subject matter e...

Ideal Companies: Shire Pharmaceuticals, Novo Nordisk, Pfizer, AstraZeneca, Endo, Sanofi

Tags for this Online Resume: Internal audit, Training, Risk Management, Governance, Internal Control, Change Management, Risk Assessment, Facilitation, External Benchmarking, Communication through writing, Thought Leader, Team Player, Project Leader, Business Liaison, Contract Analyst, Assurance, Risk Profiles, Compliance

Clinical Pharmacovigilance/Drug Safety - 7 Years of Experience - Near 94116

Tags for this Online Resume: neurology, medical, ICH-GCP, FDI, SOP, clinical trials, adverse event, analytical

Director - 7 Years of Experience - Near 46229

• Self-motivated with progressive experience in coordinating activities with the Joint Commission, Department of Child Services, CMS full-scale surveys; understands regulatory communication, plan of corrections, and follow up. • Planned, staffed, implemented, prioritized, controlled, evaluated projects, and coordinated task levels to complete projects within deadlines. • Strong organization and project management skills wit...

Tags for this Online Resume: Performance Improvement, Risk Management, CPHQ, Quality healthcare, Project Management

drug safety Associate

Management and processing of expedited adverse event reports to include the entry of safety data into adverse database and tracking systems, review of adverse events for completeness, accuracy and appropriateness for expedited reporting, generation of queries directly with sites for follow-up information reporting of expedited adverse events. Assessed and triage all incoming cases and process accordingly

Tags for this Online Resume: argus, Web base Data , medDRA, microsoft office, Oncology

Pharmacovigilance/Drug Safety - 13 Years of Experience - Near 19380

Pharmacovigilance professional with over 10 years experience in product safety roles of increasing responsibility seeking further career growth opportunities

Tags for this Online Resume: Argus Experience, Pharmacovigilance, Validation, adverse event managment, submission to health Authorities

Featured Profile

Pharmacist - 13 Years of Experience - Near 33713

To obtain an interactive position encompassing medication therapy review, medication cost containment and alternative formulary proposals. To apply experience and expertise to counsel and educate patients pertaining to disease states in addition to implementing compliance tools to obtain the best outcome possible. My success has been defined by my dedication, respectful approach to patient care and adaptability to new w...

Ideal Companies: Veterans Administration, Humana, Baycare

Tags for this Online Resume: Pharm D, Consultant, Medication Therapy Management, St. Petersburg, Work from home, Excellant communication skills, Self-motivator, Flexible

Featured Profile

Registered Nurse - 40 Years of Experience - Near 89131

I am considered to be a leader, and always eager to be involved in new projects. I have particular interest in patient experience and satisfaction. I would like to move further up the corporate ladder. By taking ideas and turning them into action plans, the healthcare facility would be able to realize an increase in revenue and in addition have satisfied patients who will recommend their facility to others in the community.

Ideal Companies: University Medical Center, HealthInsight, VHS Consolidated

Tags for this Online Resume: communication with senior leadership, resolution of patient complaints using staff and family education, regulatory specialist, Microsoft Word, Excel, PowerPoint

Clinical Research - 20 Years of Experience - Near 33406

• Clinical Research Consultant with over 28 years of Pharmaceutical/Biotech experience including Phase I – III clinical trial development with direct involvement in multiple FDA/ICH submissions leading to six NDA approvals. • Extensive monitoring domestically and internationally, training and mentoring innumerable CRAs/Monitors in the field which lead to further training responsibilities with Study Teams and Management Te...

Tags for this Online Resume: Florida, Pharmaceutical Research, Monitoring, Management, Team Building

Featured Profile

Clinical Research - 6 Years of Experience - Near 92649

Experienced Clinical Research Professional interested in positions within the pharmaceutical or medical device industry.

Ideal Companies: inventiv, johnson & johnson, covance, covidien, peregrine

Tags for this Online Resume: Irvine, CCRP, regulatory affairs, clinical project manager, EDC, budgets , timelines, contracts and budgets

Clinical Pharmacovigilance/Drug Safety - 5 Years of Experience - Near 39056

Tags for this Online Resume: Argus 7.0.3, Adverse event reporting, MedDRA conventions, Microsoft Office, ICH-Guidelines, Communication skills, Arisg

Featured Profile

Clinical Research - 15 Years of Experience - Near 90001

I am seeking a position in Clinical Trial Management or as a Project Manager per my previous US and international experience.

Ideal Companies: Pharmaceutical or Biotech

Tags for this Online Resume: Oncology, Orthopedics, Surgical, Clinical Research, Management, Medical, Medical Affairs, Diabetes, Cardiovascular, Women's Health, Clinical Trial Management, Regulatory, Medical Writing, Microsoft, CTMS

Clinical Pharmacovigilance/Drug Safety - 4 Years of Experience - Near L6Y 0K6

SKILL SUMMARY * Medical Physician with over 7 years of experience in world class hospital and multinational Contract research organization (CRO) highly result oriented with successful completion of multiple clinical research projects, managed and reported Serious Adverse Events (SAE) and Adverse Events (AE) to various regulatory bodies. Hand on experience on project review and overall project management. * Proven track reco...

Tags for this Online Resume: Cardiopulmonary resuscitation (CPR), Clinical Research, Compliance, Hindi Language, ICU, Inventory, Leadership, Logistics