Senior, Medical Monitor

Biorasi; Leeds; On-site; GBP 70,000 - 90,000; Full time

Job summary

A clinical research organization in the UK is seeking a Medical Monitor to oversee clinical studies, provide medical expertise, and lead data reviews. The ideal candidate has a medical degree (MD or DO), fluent English skills, and 5-7 years of experience in the life sciences or related field. Responsibilities include regulatory submissions, medical training, and project management. If you are passionate about clinical research and thrive in a collaborative environment, this opportunity is for you.

Qualifications

• 5-7 years’ work experience within the life science industry or related field.
• Minimum 4 years’ experience with medical monitoring services.
• Keen knowledge and understanding of ICH GCP.

Responsibilities

• Act as a primary or backup Medical Monitor for assigned clinical studies.
• Oversee multiple studies and contribute to regulatory submissions.
• Lead medical review and interpretation of clinical and safety data.

Skills

Medical monitoring services

Fluent English

Verbal communication skills

Written communication skills

Critical Thinking

Proficiency in Microsoft Office

Education

Medical degree, MD or DO

Tools

Safety databases (ARISg, Oracle Argus)

EDC systems (IBM, Medrio, Medidata)

Job description

We are Growing! Let us support your career journey the Biorasi way. Innovative, Collaborative, Dynamic and Evolving. Capitalizing on your strengths while encouraging work-life balance. Biorasi is an award-winning, customer-focused, full-service clinical research organization.

Biorasi is looking for top performers who are as passionate about clinical research as we are – clinical trial veterans and industry newcomers who will thrive in our fast‑paced environment and help us drive new therapies to patients. Here is your chance to become a vital part of a growing global company in the expanding clinical research industry.

Your role:

• Act as a primary or backup Medical Monitor for the assigned clinical studies.
• Oversee multiple studies, contribute to the regulatory submissions (INDs, etc.).
• Responsible for providing protocol / therapeutic training to the study team, as required.
• Provide medical expertise to investigators and study team and advise on medical related questions.
• Perform eligibility review of the study subjects, as required.
• Lead in medical review, assessment, and interpretation of clinical and safety data to ensure that the data are correct and presented with the appropriate medical interpretation. Escalate any critical safety concerns to the study team and Sponsor, and coordinate between sites and study team / Sponsor.
• Responsible for identifying, reviewing and confirming protocol deviation classification.
• Lead the Medical Monitoring and Protocol deviation project meetings, participate in any other Sponsor calls, if required.
• Work closely with Safety and Pharmacovigilance team to provide medical input into safety reports including SAE narratives and analysis of similar events, periodic safety reports.
• Responsible for the review of individual data with SAEs and potentially clinically important laboratory test results or vital sign abnormalities and escalate issues to the Sponsor as needed.
• Assist in medical and scientific review of deliverables such as TLFs and CSR.
• Lead in developing and maintaining SOPs, Templates, and study plans.
• Participate in the review of the design and conduct of clinical trials including the development and review of protocols and amendments.
• Assist in incorporating medical strategy into study feasibility required for new projects.
• Cooperate with program development and commercial teams to develop the medical strategy for the RFP for new projects.
• Participate and lead medical strategy section in the Bid Defence preparation and meetings.
• Responsible for Line Management of assigned team members in Medical and Scientific Affairs group.
• Support regulatory inspections and audits as needed.
• Perform other duties for the Medical & Scientific Affairs branch, as assigned.

Your profile:

• Medical degree, MD, DO or its international equivalent.
• Fluent English (oral and written).
• Proven 5-7 years’ work experience within the life science industry or related field.
• Minimum 4 years’ experience with medical monitoring services.
• Keen knowledge and understanding of ICH GCP.
• Excellent verbal, written communication and presentation skills.
• Critical Thinking and background medical and scientific research.
• Strong proficiency in using Microsoft Office.
• Experience with safety databases (ARISg, Oracle Argus, etc.) and / or EDC system (IBM, Medrio, Medidata) a plus.

If you have the experience required and want to join an energetic, creative, and collaborative team, please apply directly to our website at https://biorasi.com or email us at [e-mail].

Biorasi is committed to creating a diverse environment and is proud to be an equal‑opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status. Biorasi is also committed to compliance with all fair employment practices regarding citizenship and immigration status.