TFS HealthScience is a global, mid-sized contract research organization (CRO) partnering with biotechnology and pharmaceutical companies across the full clinical development lifecycle. Our expertise spans full-service clinical development, project-based support, strategic resourcing, and Functional Service Provider (FSP) solutions, matching experienced professionals to roles where they deliver the greatest impact. 

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.

In this position, you will play a key role in the operational execution of clinical studies, contributing to the safe, effective, and responsible development of new therapies. You may also take on Study Lead responsibilities for national and international trials, depending on project needs.

Key Responsibilities

• Independently plan, conduct, and follow up on pre-study, site initiation, routine monitoring, and close-out visits, both on-site and remotely, in line with the applicable monitoring plan

• Oversee study site performance, including recruitment progress, and provide ongoing support to sites on study-related questions and operational issues

• Review eCRF data, timelines, and queries; identify and report protocol deviations; and maintain clear communication with project management and sponsors

• Review and maintain study documentation at site level, including Investigator Site Files (ISF), ensuring inspection readiness and compliance with applicable regulations

• Collaborate cross-functionally with medical, project management, quality management, and data management teams, and support sites during audits and inspections

Qualifications

• Degree in a scientific or medical discipline, or completed vocational training in a relevant healthcare or medical field

• Additional training in clinical research or CRA certification, combined with several years of experience as a Clinical Research Associate

• Strong knowledge of GCP, ICH guidelines, and clinical research processes, with a high level of accuracy in handling study data and regulatory requirements

• Fluent German and English language skills, both written and spoken, with willingness to travel nationally and internationally as required

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.