Clinical Project Manager

TN United Kingdom; United Kingdom; Remote; GBP 40,000 - 60,000; Full time

Job summary

A leading company in the life sciences sector is seeking a Clinical Project Manager to join their UK team in a remote position. The role involves managing clinical research studies, ensuring compliance, and collaborating with global stakeholders. Ideal candidates will have a Bachelor's Degree and experience in the clinical/healthcare industry, with strong project management skills and attention to detail.

Qualifications

• Experience in the clinical/healthcare industry, preferably in clinical research.
• Ability to handle multiple projects and meet deadlines.

Responsibilities

• Support start-up, management, and completion of patient services for clinical research studies.
• Communicate regularly with global study stakeholders, managing expectations and escalations.
• Prepare study-specific documentation and train sites and study teams.

Skills

Project Management

Clinical Trial Processes

Communication

Problem-Solving

Attention to Detail

Education

Bachelor’s Degree or equivalent experience

Job description

Social network you want to login/join with:

Company Background

Established in 1996 and rebranded to Scout in 2024, we built our foundation on planning meetings for numerous organizations within the life sciences sector (Scout Meetings).

In response to emerging industry needs, we expanded our services to include Scout Clinical, a top provider of clinical trial patient travel and reimbursements, and Scout Academy, a secure, online, on-demand learning management system ensuring global compliance.

Company Recognition

Scout is recognized as a leader in innovation, attention to detail, and for our stellar team members. We aim to make the complex easier. If this interests you, we’d love to have you join our rapidly growing team!

Position Summary

We are hiring a talented and eager Clinical Project Manager to join our UK team in a remote position.

Responsibilities

1. Support start-up, management, and completion of patient services for clinical research studies.
2. Review protocols for new requests for proposal or assigned projects.
3. Manage study activities and start-up processes.
4. Maintain study tracking databases to reflect study status and deliverables.
5. Communicate regularly with global study stakeholders, including CROs and Sponsors, managing expectations and escalations.
6. Lead study meetings, including Kick-off and Investigators’ Meetings.
7. Act as the main contact for Sponsor and CRO clients regarding Scout Clinical services.
8. Collaborate on operational policies and ensure adherence.
9. Oversee regulatory onboarding processes with the Clinical Compliance Team.
10. Prepare study-specific documentation and train sites and study teams on the Scout portal.
11. Manage portal configurations and support travel and reimbursement activities.
12. Review and manage study utilization and financial metrics.

Candidate Requirements

• Bachelor’s Degree or equivalent experience.
• Experience in the clinical/healthcare industry, preferably in clinical research.
• Strong understanding of project management and clinical trial processes.
• Ability to handle multiple projects and meet deadlines.

Desired Skills and Qualities

• Desire to learn and be coachable.
• Timely, professional, courteous communication.
• Attention to detail and organizational skills.
• Ability to prioritize and work under pressure.
• Problem-solving and critical thinking abilities.
• Team-oriented mindset.

Visit our website at www.scoutclinical.com or follow us on LinkedIn for more opportunities.

We are an equal opportunity employer. Powered by JazzHR.