Job Description
・General monitoring activities of medical institutions conducting clinical trials under GCP
・Smooth communication activities with clinical trial staff including principal investigators
・Ensuring reliability of clinical trial data
Required Skills:
Accountability, Clinical Data Interpretation, Clinical Evaluation Reports, Clinical Medicine, Clinical Research Methods, Clinical Study Management, Clinical Study Protocols, Clinical Trial Planning, Clinical Trials, Clinical Trials Marketing, Clinical Trials Monitoring, Clinical Trial Support, Communication Management, Data Quality Control, Detail-Oriented, Ethical Compliance, ICH GCP Guidelines, Investigation Procedures, IS Audit, Medical Research, Protocol Development, Regulatory Requirements, Scientific Research, Therapeutic KnowledgePreferred Skills:
Current Employees apply HERE
Current Contingent Workers apply HERE
Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status:
RegularRelocation:
VISA Sponsorship:
Travel Requirements:
Flexible Work Arrangements:
HybridShift:
Valid Driving License:
Hazardous Material(s):
Job Posting End Date:
01/31/2026*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
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