Senior Manager, Clinical Trial Transparency & Disclosure (Remote)

MMS; City of Edinburgh; Remote; GBP 60,000 - 80,000; Full time

Job summary

MMS, a leading clinical research organization, is seeking a Senior Manager for Clinical Trial Transparency & Disclosure. This remote role involves interacting with clients and managing teams to ensure regulatory compliance and excellence in trial data management. Ideal candidates possess a graduate degree, extensive experience in clinical trials, and strong leadership skills to drive projects and foster innovation.

Qualifications

• Minimum 6 years’ experience in clinical trial transparency, disclosure, or medical writing.
• At least 5 years in a CRO environment.
• Demonstrated managerial skills preferred.

Responsibilities

• Interact with clients and regulatory authorities, represent at regulatory meetings.
• Lead/manage individuals and groups, coordinate transparency deliverables.
• Identify areas for improvement and propose strategic solutions.

Skills

Scientific writing

Analytical skills

Organizational skills

Problem-solving skills

Strong communication skills

Presentation skills

Education

Graduate degree in scientific, medical, clinical discipline or related field

Masters preferred

Tools

MS Office

Job description

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Senior Manager, Clinical Trial Transparency & Disclosure (Remote), Edinburgh

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Client:

MMS

Location:

Edinburgh, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

72d228773590

Job Views:

6

Posted:

25.06.2025

Expiry Date:

09.08.2025

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Job Description:

Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is an award-winning, data-focused clinical research organization (CRO).

We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate.

We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges.

With a global footprint across four continents, MMS maintains an industry-leading customer satisfaction rating and fosters a collaborative and inclusive work environment.

Join us at MMS and be part of a team shaping the future of clinical research. Discover more about our opportunities and why MMS is a great place to advance your career. Visit www.mmsholdings.com or follow MMS on LinkedIn.

Responsibilities:

• Interact with clients and regulatory authorities, remotely and onsite, including representation at key regulatory meetings on behalf of the client.
• Lead/manage multiple individuals and/or groups effectively.
• Coordinate Transparency deliverables ensuring timelines and milestones are on track.
• Assess resource utilization and forecasting to meet company goals.
• Communicate complex strategic concepts clearly to targeted audiences.
• Develop and present industry trends, benchmarking, and pertinent information to clients.
• Participate in industry events to showcase thought leadership.
• Lead strategic planning and develop contingency plans for unforeseen challenges.
• Foster positive team morale and productivity.
• Manage staff, make decisions, and advise on complex problems, understanding inter-departmental implications.
• Oversee daily activities of transparency, PLS, and redaction teams.
• Identify areas for improvement proactively and propose strategic solutions.
• Develop and lead diverse teams to achieve departmental goals.

Requirements:

• Graduate degree in scientific, medical, clinical discipline or related field; Masters preferred.
• Minimum 6 years’ experience in clinical trial transparency, disclosure, or medical writing.
• At least 5 years in a CRO environment.
• Demonstrated managerial skills preferred.
• High knowledge of drug development, clinical development, and regulatory guidelines.
• Excellent scientific writing, analytical, organizational, and problem-solving skills.
• Proficiency with MS Office.
• Strong communication and presentation skills.
• Knowledge of ISO 9001, ISO 27001, 21 CFR Part 11, FDA, and GCP requirements.
• Understanding of CROs, scientific & clinical data, terminology, and drug development process.