Associate Clinical Quality Manager Nordic-Baltic-Ireland - Copenhagen

Kun for registrerede medlemmer Copenhagen, Danmark

for 2 dage siden

Fuldtid

Job Description · The Position · We are seeking an Associate Country Clinical Quality Manager (aCCQM) to support clinical quality oversight across the Nordic Baltic Ireland (NBI) region. This role provides primary support to Norway, with additional responsibilities for Denmark, I ...

Jobbeskrivelse

Job Description

The Position

We are seeking an Associate Country Clinical Quality Manager (aCCQM) to support clinical quality oversight across the Nordic Baltic Ireland (NBI) region. This role provides primary support to Norway, with additional responsibilities for Denmark, Ireland, Sweden, Finland, Latvia, Estonia, and Lithuania.

The aCCQM contributes to ensuring patient safety, data integrity, and compliance across our clinical trials by implementing global and local quality processes, supporting inspection readiness, and driving continuous improvement across the region. You will collaborate closely with the Clinical Quality Managers, CCQMs and cross-functional partners to uphold high-quality standards and promote a culture of quality.

What will you do

Provide primary support for clinical quality activities in Norway, with additional support across NBI (Denmark, Ireland, Sweden, Finland, Latvia, Estonia, Lithuania) as needed.
Partner with CCQMs to implement and maintain quality standards aligned with global, regional, and local requirements.
Assist with audits, inspections, and ongoing quality control activities.
Coordinate, support, and deliver local training sessions.
Identify opportunities for process optimization and contribute to continuous improvement initiatives.
Serve as a point of contact for quality-related topics across the assigned countries.

Qualifications, skills & experience required

University degree.
4–6 years of clinical research experience, including roles in monitoring or clinical quality oversight.
Strong knowledge of Good Clinical Practice, GCP and clinical trials Management.
Experience supporting audits, inspections, or training delivery is considered an advantage.
Excellent communication and collaboration skills to work effectively across multiple countries and teams.
Ability to manage priorities in a dynamic, cross-functional environment.
Strong organizational and project management capabilities.
Comfortable working with new technologies and leveraging AI tools to enhance quality processes and efficiency.

Ready to take up the challenge? Apply now
Know anybody who might be interested? Refer this job

Required Skills:

Accountability, Accountability, Adaptability, Clinical Development, Clinical Medicine, Clinical Quality Management, Clinical Research, Clinical Sciences, Clinical Trial Development, Clinical Trials, Clinical Trials Monitoring, Clinical Trials Operations, Collaborative Communications, Continuous Process Improvement, Data Analysis, Dedication to Patient Care, Ethical Standards, Good Clinical Practice (GCP), ICH GCP Guidelines, Investigation Procedures, Leadership Mentoring, Management Process, Patient Safety, Process Improvements, Quality Management {+ 3 more}

Preferred 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:

Regular

Relocation:

No relocation

VISA Sponsorship:

Travel Requirements:

10%

Flexible Work Arrangements:

Hybrid

Shift:

Not Indicated

Valid Driving License:

Hazardous Material(s):

n/a

Job Posting End Date:

03/2/2026

*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.