Medical Affairs Drug Safety Jobs

GForce Life Sciences - Princeton, NJ, United States

preferred to be in Bachelor of Science or related healthcare degree 1-3 years of Submission Experience Demonstrated proficiency in safety database functionality *Drug Safety experience is defined as actual

from: linkedin.com - 22 days ago

Pfizer - Cambridge, Massachusetts (+4 locations)

, Worldwide Medical, Drug Safety Research and Development and Safety in order to drive TA Medical Strategy across the organization. **ROLE RESPONSIBILITIES** This position reports directly to **Head of Oncology

from: HealtheCareers.com - 14 days ago

Planet Pharma - , NC, United States

(in cooperation with Medical Affairs). Responsible for review of investigational product release-enabling documents. Primary or secondary responsibility for training company employees in regulatory practices

from: linkedin.com - 22 days ago

GForce Life Sciences - Princeton, NJ, United States

preferred to be in Bachelor of Science or related healthcare degree 1-3 years of Submission Experience Demonstrated proficiency in safety database functionality *Drug Safety experience is defined as actual

from: linkedin.com - 24 days ago

Incyte Corporation - Chadds Ford, Pennsylvania, USA

, Biostatistics, and Drug Safety/ Pharmacovigilance Department, Sales Training). Participate in the design, conducting, analysis, and reporting of Medical Affairs led clinical trials and observational studies

from: Ivyexec.com (+1 source) - 13 days ago

Pfizer - San Francisco, CA

- drug product and device/IVD SMEs. Quality Assurance GCMC (Regulatory) Medical Affairs Safety PGS - manufacturing sites and post launch device team. External designers and contract manufacturing USD 161,600.00 - 269,400.00 per year

from: Dice.com - 15 days ago

Johnson and Johnson - Titusville, NJ

, Medical Affairs) * Demonstrated skills in clinical medicine with at least 1 year of clinical practice experience * Board Certification (if US) preferred; Medical specialization preferred * Neuroscience

from: Johnson and Johnson - 4 days ago

AbbVie - Irvine, California (+1 location)

is responsible for the management of a RDQA global Safety, Regulatory Affairs (RA) and Medical Affairs (MA) QA team which provides independent quality oversight of GxP activities, covering the AbbVie drug, device

from: resume-library.com - 22 days ago

Thermo Fisher Scientific - Remote, NC

) of the following key areas: Medical affairs Clinical development in biopharma/biotech (especially peri- or post-approval late phase interventional studies) Medical device development (in-vitro diagnostics, SaaMD

from: Dice.com - 23 days ago

Emergent Biosolutions - Gaithersburg, MD, US

reports including medical analysis. • Thorough understanding of the cross functional drug development processes (Clinical Operations, Biometrics, and Regulatory Affairs) and context applicable to safety

from: Emergent Biosolutions - More than 30 days ago