Project Management Associate (Pma)

TFS HealthScience; Ledston; On-site; GBP 28,000 - 42,000; Full time

Job summary

TFS HealthScience is recruiting a Project Management Associate in the United Kingdom to support Project Managers and study teams across clinical trials, collaborating with sponsors and CRO partners. You will help plan, set up, execute and close-out studies, maintain CTMS records, trackers and study files, and coordinate meetings, minutes and newsletters.

This entry-level role offers a clear path toward a Project Manager career, with exposure to vendor management, regulatory submissions and

Qualifications

• CTA or similar entry-level CRO role experience.
• Interest in advancing to a Project Manager career.
• Strong English communication skills.
• Comfortable in client-facing environments.
• Motivated to develop and grow professionally.

Responsibilities

• Support planning, setup, execution, and close-out of clinical studies while meeting timelines and regulatory standards.
• Maintain study documentation, CTMS records, trackers, logs, and study files.
• Provide administrative and operational support to Project Managers and CRAs.
• Coordinate study communications, meetings, agendas, minutes, and newsletters.
• Assist with vendor management, investigator payments, invoice tracking, and financial reconciliation.
• Support regulatory submissions, audits, inspections, and translations.
• Coordinate study logistics and investigator meetings.

Skills

CTA experience

Client-facing

English communication

Career development mindset

Interest in AI tools

Tools

Excel

Job description

About this role

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full-service capabilities, resourcing, and Functional Service (FSP) solutions.

The Project Management Associate (PMA) is aligned to and managed under the assigned therapeutic business unit. The PMA will function operationally as a member of the study team and provide administrative support to the Project Manager (PM)

Key Responsibilities

• Support the planning, setup, execution, and close-out of clinical studies, ensuring timelines, quality standards, and regulatory requirements are met.
• Maintain study documentation, CTMS records, contact lists, trackers, logs, and study files.
• Provide administrative and operational support to Project Managers, Clinical Research Managers, and CRAs.
• Coordinate study communications, meetings, agendas, minutes, presentations, and newsletters.
• Assist with vendor management, investigator payments, invoice tracking, and financial reconciliation.
• Support regulatory submissions, audits, inspections, and document translation processes.
• Coordinate study logistics, supplies, and investigator meeting activities.
• Act as a central point of contact for study teams and sponsors, fostering effective collaboration and communication.

Qualifications

• Previous experience as a CTA or in another entry-level role within a major CRO, such as ICON, PPD, IQVIA or Syneos Health.
• Motivated individuals looking to develop their careers, take on new challenges and grow professionally.
• A genuine interest in progressing toward a Project Manager career path in the long term.
• Strong Excel skills, including experience managing multiple trackers and spreadsheets, as well as using formulas, pivot tables and macros.
• Interest in leveraging AI tools to improve efficiency, streamline processes and generate innovative ideas.
• Strong English communication skills.
• Comfortable working in a client-facing environment.

What We Offer

We provide opportunities for personal and professional growth in a rewarding environment. You will join a team that values collaboration, quality, and making a difference in the lives of patients.

Our core values of Trust, Quality, Passion, Flexibility, and Sustainability guide our decisions and shape our culture. By aligning on these values, we foster collaboration, innovation, and a shared commitment to excellence. Together, we make a difference.

A bit more about us

Our journey began over 30 years ago in Sweden, in the city of Lund. As a full-service global CRO, we build solution-driven teams working toward a healthier future. Bringing together over 600 professionals, TFS delivers tailored clinical research services in more than 50 countries, offering flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology, Neuroscience, Oncology, and Ophthalmology.