Senior Project Manager

MAC Clinical Research; United States; Remote; GBP 65,000 - 90,000; Full time

Benefits offered by this job

Health Insurance

Eye Care Vouchers

Cycle to work scheme

Free parking

Birthday leave

Job summary

MAC Clinical Research is seeking an experienced Global Senior Project Manager to join our growing UK-based team. This home-based role offers leadership of full-service projects in a fast-paced CRO environment, with oversight of timelines, risks and client communications.

You will collaborate with the Head of Project Management to deliver high-quality programmes, manage project teams, and ensure client satisfaction while maintaining regulatory compliance and efficient study delivery.

Qualifications

• 5-7 years industry experience including at least 3 years in full-service Project Management roles in clinical trials within a CRO, pharmaceutical or biotech setting (essential)
• Degree or similar related life science qualification or equivalent combination of education and experience (essential)
• Good knowledge of the drug development process, regulatory and ICH GCP guidelines and their application to clinical trials (essential)
• Detailed and proactive approach to risk and issue management
• Superior time management skills for working within a fast-paced environment

Responsibilities

• Working with the Head of Project Management to ensure the successful delivery of full-service projects or programmes of work, by application of project management principles and implementation of project management methodologies and processes.
• Leadership of project teams on full-service projects to ensure that project objectives are met.
• Client management and communication lead.

Skills

Project management

Clinical trials knowledge

Communication

Education

Degree in life sciences

Job description

Are you an experienced global Senior Project Manager whos’ looking for an opportunity to join a growing global CRO based in the UK? Come and join our Project Management team at MAC Clinical Research. We have an exciting new opportunity for a Senior Project Manager in line with our expanding portfolio.

This role is home based and therefore we require you to have a set up at home that allows you to work comfortably. This includes an appropriate desk and chair (excl. IT equipment which we will provide). By proceeding with your application, you are confirming you are able to do this.

KEY SKILLS, KNOWLEDGE AND QUALIFICATIONS REQUIRED:

• 5-7 years industry experience including at least 3 years in full-service Project Management roles in clinical trials within a CRO, pharmaceutical or biotech setting (essential)


• Degree or similar related life science qualification or equivalent combination of education and experience (essential)


• Good knowledge of the drug development process, associated regulatory and ICH GCP guidelines and their application to clinical trials (essential)


• Detailed and proactive approach to risk and issue management


• Superior time management skills for working within a fast-paced environment

RESPONSIBILITIES:

• Working with the Head of Project Management to ensure the successful delivery of full-service projects or programmes of work, by application of project management principles and implementation of project management methodologies and processes.


• Leadership of project teams on full-service projects to ensure that project objectives are met.


• Client management and communication lead.

BENEFITS:

• Competitive salary in keeping with pharmaceutical industry standards that will reflect experience


• Health Insurance


• Eye Care Vouchers


• Cycle to work scheme


• Free onsite parking


• 25 days annual leave (increasing in increments to 30 days after 6 years' service)


• Your birthday off work

MAC Clinical Research invites applications from highly motivated candidates, with a desire to fulfil their full potential. You will be working with an organisation that sees you as an investment and is keen for you to achieve your career aspirations.

Please email [e-mail] should you require any special arrangements or reasonable adjustments to be made throughout this selection process. This will enable us to accommodate your request as necessary.