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A leading company is seeking a highly organised Clinical Trial Coordinator to ensure comprehensive trial and site administration. The role involves tracking essential clinical documents and managing supplies, requiring strong organisational, communication, and documentation skills, ideally with relevant educational background and experience in clinical research.
Job Description
We are seeking a highly organised and detail-oriented Clinical Trial Coordinator (CTC) to join our team. Reporting to the CTC Manager, this role is responsible for ensuring comprehensive trial and site administration, including the preparation, collation, distribution, and archiving of clinical documents. The CTC will also support clinical and non-clinical supply management and ensure the timely maintenance of tracking and reporting tools.
Key Responsibilities:
Required Skills:
Education and Experience:
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):
Required Skills:
Accountability, Accountability, Analytical Problem Solving, Budget Proposals, Clinical Data Management, Clinical Documentation, Clinical Information Systems, Clinical IT, Clinical Reporting, Clinical Research, Clinical Research Coordination, Clinical Testing, Clinical Trial Compliance, Clinical Trial Documentation, Clinical Trial Management, Clinical Trials Monitoring, Clinical Trials Operations, Clinical Trial Support, Data Analysis, Drug Regulatory Affairs, ICH GCP Guidelines, Management Process, Medical Records Management, Nursing, Project Management {+ 4 more}Preferred Skills:
Job Posting End Date:
07/12/2025*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.