Medical Affairs BA

E-Solutions; United Kingdom; On-site; GBP 60,000 - 80,000; Full time

Job summary

A leading consulting firm in the United Kingdom is seeking an experienced project manager with a strong background in business analysis and regulatory compliance. The ideal candidate has about 10 years of experience in the medical or pharmaceutical industry and familiarity with AI/Agentic AI projects. The role involves collaborating with medical experts, managing project timelines, and ensuring adherence to regulations. This position also requires excellent organizational and interpersonal skills.

Qualifications

• Candidates should have about 10 years of experience in business consulting or project delivery.
• Significant exposure to the medical, life sciences, or pharmaceutical industry is crucial.
• Knowledge of regulatory processes, medical content, and compliance frameworks including GxP.

Responsibilities

• Collaborating with medical experts, CROs, vendors, and internal teams.
• Developing project plans, defining objectives, and managing timelines and budgets.
• Ensuring all projects adhere to relevant regulations and guidelines.
• Coordinating data collection, ensuring data quality and integrity.
• Overseeing clinical trials and other research initiatives from start-up to database lock.

Skills

Project management

Business analysis

Stakeholder management

Data management

Regulatory compliance knowledge

Familiarity with AI/Agentic AI

Job description

Inputs from manager on customer expectation: for your information

• Is familiar with/has worked with AI/Agentic AI projects (Must)
• Has worked with Medical Affairs previously and is aware of how that differs from commercial
• Is mid-level experienced (not extremely junior but also no requirement for very senior folks)

Generic JD:

Role Expectation: Strong project management and Business Analysis, including planning, execution, and communication, excellent organizational and interpersonal skills, and the ability to work independently and as part of a team.

Is familiar with/has worked with AI/Agentic AI projects.

Stakeholder Management: Collaborating with medical experts, clinical research organizations (CROs), vendors, and internal teams.

Project Planning and Execution: Developing project plans, defining objectives, and managing timelines and budgets.

Regulatory Compliance: Ensuring all projects adhere to relevant regulations and guidelines (e.g., FDA, ICH).

Data Management: Coordinating data collection, ensuring data quality, and data integrity.

Study Management: Overseeing clinical trials, NIS studies, and other research initiatives from start-up to database lock.

Experience & Knowledge: Candidates should have about 10 years of experience in business consulting or project delivery, with significant exposure to the medical, life sciences, or pharmaceutical industry. They must demonstrate knowledge of regulatory processes, medical content, and compliance frameworks including GxP. Familiarity or experience in AI/Gen AI projects.