Job Description

We are currently looking for a Clinical Research Manager (CRM) Lead

Responsibilities

• Will lead one or several therapeutic areas of the growing portfolio in the country

• Accountable for the successful execution, enrollment and quality of their clinical trial portfolio

• Accountable to ensure performance metrics, timelines and key milestones are met in compliance with ICH/GCP and country regulations, our company’s policies and procedures, quality standards and adverse event reporting requirements internally and externally.

• Accountable to develop operational strategies and quality plans for the conduct of all programs and studies in the therapeutic areas’ portfolio.

• Collaborates with other directors, local and regional stakeholder in GCTO in order to develop and build territory of principal investigators and sites.

• Lead a team independently with supervision from Clinical Research Director to high performance.

• Supports strategic initiatives across country, Global Clinical Development GCD and GCTO

• Main Point of Contact (POC) for assigned protocols and link between Country Operations and Clinical Trial Team (CTT).

• Responsible for project management of the assigned studies: pro-actively plans, drives and tracks execution and performance of deliverables/timelines/results to meet country commitments from feasibility and site selection, recruitment, execution and close out.

Qualifications

• 10+ years of experience in clinical research with demonstrated success and increasing responsibilities of which 5+ years consisted of leading projects and team

• Bachelor degree in Science (or comparable)

• Expertise in project and site management. The position requires demonstrated successful implementation of project management skills at program and site level.

• Strong organizational skills with demonstrated success required.

• Requires a complete understanding of ICH GCP and global/regional/local regulatory

• environment.

• Proficiency in written and spoken English and Greek.

• CRA Experience is preferred

• Advanced degree, (e.g., Master degree, MD, PhD) is preferred

We offer an attractive compensation package, outstanding benefits, and an exciting work environment with varied tasks in an international environment.

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:

Regular

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Hybrid

Shift:

Valid Driving License:

Hazardous Material(s):

Required Skills:

Adaptability, Clinical Research, Clinical Research Management, Clinical Trial Documentation, Clinical Trial Management, Clinical Trial Management Processes, Clinical Trial Planning, Clinical Trials Monitoring, Clinical Trials Operations, Cross-Cultural Awareness, Decision Making, Ethical Standards, Good Clinical Practice (GCP), Oncology Trials, Oracle CRM, People Leadership, SAP CRM

Preferred Skills:

Job Posting End Date:

09/1/2025

*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.