Good pharmacoepidemiology practice (gpp) compliance
Vendor document review and quality control
Merck & Co., Inc. is seeking a Senior Specialist in Medical Affairs for a temporary position that involves managing operational activities for observational research studies. The role requires a collaborative individual with a background in clinical or observational research, who can effectively communicate and manage projects in a hybrid work environment
Job Summary
This position is responsible for coordinating the end-to-end process for executing observational or non-interventional research studies in compliance with Good Pharmacoepidemiology Practice.
The role involves managing study timelines, overseeing outsourced vendors, and ensuring the integrity of study data for reports and publications.
Candidates must possess a Bachelor's degree in a health-related discipline and at least 2 years of experience in clinical or observational research.
Matching Summary
Match Score: 85
Merck & Co., Inc. is seeking a Senior Specialist in Medical Affairs for a temporary position that involves managing operational activities for observational research studies. The role requires a collaborative individual with a background in clinical or observational research, who can effectively communicate and manage projects in a hybrid work environment.
Skills & Requirements
Must-have
End-to-end observational study execution
Good Pharmacoepidemiology Practice (GPP) compliance
Vendor document review and quality control
Protocol and report preparation support
Study timeline and milestone tracking
Nice-to-have
Strong project management and prioritization skills
Ability to work independently and collaboratively
Understanding of digital innovation
Excellent communication and interpersonal skills
Troubleshooting issues with internal partners
Key Requirements
Bachelor's degree in Nursing, Biology, Public Health, or science
2+ years of work experience in clinical/observational research