Senior Manager, Clinical Trial Transparency & Disclosure (Remote)

MMS; Manchester; Remote; GBP 60,000 - 90,000; Full time

Job summary

MMS, a leading clinical research organization, seeks a Senior Manager for Clinical Trial Transparency & Disclosure. In this remote role, you will lead teams, interact with clients, and manage transparency deliverables. The ideal candidate will possess a graduate degree and extensive experience in clinical trial settings, alongside exceptional problem-solving and communication skills.

Qualifications

• Minimum 6 years’ experience in clinical trial transparency or medical writing.
• Managerial skills preferred.
• High knowledge of drug development and regulatory guidelines.

Responsibilities

• Interact with clients and regulatory authorities.
• Lead/manage multiple teams in a global environment.
• Assess resource utilization and meet company-wide goals.

Skills

Analytical

Problem Solving

Communication

Presentation

Organizational

Education

Graduate degree in scientific, medical, clinical discipline

Tools

MS Office

Job description

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

Client: MMS

Location: Manchester, United Kingdom

Job Category: Other

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EU work permit required: Yes

Job Reference:

61b8c6274c97

Job Views:

26

Posted:

22.06.2025

Expiry Date:

06.08.2025

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-leading 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 where employees can thrive.

Join us at MMS and be part of a team that is shaping the future of clinical research.

Discover more about our exciting 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.
• Demonstrated ability to lead/manage multiple individuals and/or groups.
• Cross-functionally collaborate and coordinate Transparency deliverables ensuring that timelines and milestones remain on track.
• Assess resource utilization and forecasting to meet companywide goals.
• Communicate complex strategic concepts effectively, tailoring messages to the audience.
• Develop and present industry trends, benchmarking, and pertinent information to clients.
• Participate in industry events as needed.
• Lead and manage teams in a global environment, ensuring strategic planning and contingency measures.
• Facilitate positive team morale and productivity.
• Manage staff, make decisions, and advise on complex problems, considering interdepartmental implications.
• Oversee daily activities of the 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 of 6 years’ experience in clinical trial transparency, disclosure, or medical writing; at least 5 years in a CRO environment.
• Managerial skills and experience 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.