Medical Information Lead

JR United Kingdom; Maidenhead; On-site; GBP 60,000 - 100,000; Full time

Job summary

An established industry player is seeking a passionate Medical Information Lead to oversee their Medical Information function. In this pivotal role, you will ensure compliance and high standards while managing a third-party medical information agency. Your expertise in medical and regulatory standards will be crucial as you develop accurate responses to medical inquiries and lead post-trial access programs. This is a unique opportunity to make a significant impact within a dynamic team, contributing to the delivery of high-quality medical information and enhancing patient outcomes.

Qualifications

• Proven experience in Medical Information within the pharmaceutical or biotechnology industry.
• Strong understanding of medical and regulatory standards.

Responsibilities

• Provide strategic and operational leadership for the Medical Information function.
• Manage and maintain oversight of our third-party medical information agency.

Skills

Medical Information Experience

Regulatory Standards Knowledge

Communication Skills

Vendor Management

Post-Trial Access Programs

Job description

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Medical Information Lead

We are seeking a highly motivated and experienced professional to lead our Medical Information function. In this pivotal role, you will be responsible for overseeing all Medical Information activities, ensuring compliance, consistency, and high standards across the function.

Key Responsibilities:

1. Provide strategic and operational leadership for the Medical Information function
2. Manage and maintain oversight of our third-party medical information agency
3. Develop scientifically accurate and compliant responses to second-line medical enquiries
4. Draft and review standard response letters to ensure clarity and consistency
5. Ensure robust oversight, tracking, and reporting across all Medical Information activities
6. Lead the management of our Post-Trial Access Program, ensuring ethical and efficient implementation

Requirements:

1. Proven experience in Medical Information within the pharmaceutical or biotechnology industry
2. Strong understanding of medical and regulatory standards
3. Excellent written and verbal communication skills
4. Ability to manage vendors and ensure service-level excellence
5. Experience with post-trial access or compassionate use programs is an advantage

If you’re passionate about delivering high-quality medical information and want to make an impact, we’d love to hear from you.

About Planet Pharma:

Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its headquarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.

Our specialist knowledge and close relationships with our clients and the wider industry really make us unique in our field. Recently, we were recognized by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry bodies for our commitment to excellence and service delivery. We have extensive expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions, Clinical Development, Quality, Biostatistics, and Medical Affairs / Writing.

We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of race, sex, disability, religion/belief, sexual orientation, or age.