Logo for TFS HealthScience - Contract Research Organization

Clinical Trial Manager - Freelance

Role overview

Qualifications

  • Degree in Life Sciences, Pharmacy, Medicine, or similar
  • 5+ years’ experience in clinical research
  • Experience as CRA and/or in project management
  • Strong knowledge of GCP, ICH, and regulatory requirements

Responsibilities

  • Support study start-up activities (feasibility, site selection, regulatory submissions)
  • Assist in building and maintaining study timelines and plans
  • Coordinate investigator meetings and support site activation
  • Oversee day-to-day trial operations across sites/countries

Key facts

  • Remote from: Europe
  • Freelance
  • Senior (5-10 years)
  • 0
  • English

Other skills

  • Communication
  • Problem Solving

About the company

TFS HealthScience - Contract Research Organization logo

TFS HealthScience - Contract Research Organization

TFS HealthScience is a full-service, global Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies to advance innovative treatments and improve patient outcomes. With over 800 professionals operating across 40 countries, TFS delivers tailored clinical research services in specialized therapeutic areas, including dermatology, internal medicine, neuroscience, oncology, and ophthalmology. Dedicated to empowering partners and enriching lives, TFS offers flexible solutions that combine global reach with the agility and responsiveness of a mid-sized CRO. For more information, visit www.tfscro.com.

Company details

Company size501 - 1000

Your match analysis

See how your profile stacks up against this role.

We compared the job requirements to your profile to show where you're strong and where you fall short.

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.

Clinical Trial Manager ensures that studies are delivered on time, within budget, and in compliance with regulatory requirements and GCP standards.

As part of our SRS/FSP team, you will be dedicated to one sponsor, a global pharmaceutical or biotechnology company that is an industry leader within its therapeutic area.

Please, keep in mind that this is a part-time opportunity directed at Freelance Professionals only.

Key Responsibilities

  • Support study start-up activities (feasibility, site selection, regulatory submissions)

  • Assist in building and maintaining study timelines and plans

  • Coordinate investigator meetings and support site activation

  • Oversee day-to-day trial operations across sites/countries

  • Ensure compliance with ICH-GCP and regulatory requirements

  • Monitor study progress, enrollment, and data quality

  • Identify risks and escalate as needed

  • Ensure audit/inspection readiness and quality standards

  • Review clinical data and support reporting to sponsors

  • Contribute to study reports and documentation

Qualifications

  • Degree in Life Sciences, Pharmacy, Medicine, or similar

  • 5+ years’ experience in clinical research

  • Experience as CRA and/or in project management

  • CRO experience is an advantage

  • Strong knowledge of GCP, ICH, and regulatory requirements

  • Strong communication, coordination, and problem-solving skills

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.

Apply once. Then go straight to the hiring manager.

After you apply, unlock the direct contact details of the people who actually make the call. A quick follow-up makes you 5x more likely to land an interview.

MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
Unlocked after you apply
·

Related jobs

Other jobs at TFS HealthScience - Contract Research Organization

Premium

Reach out to the hiring manager directly.

Gain access to the contact details of the hiring managers who actually decide, and reach out to network with them directly. That, plus more when you upgrade:

  • Full match report with fit score and gaps
  • Career diagnostics on how recruiters read you
  • Curated company matches and warm intros
  • 48h early access to new roles

Cancel anytime.