Clinical Scientist - Freelance at TFS HealthScience

Copenhagen, Capital Region of Denmark, Denmark -

Full Time

Start Date

Immediate

Expiry Date

08 Mar, 26

Salary

0.0

Posted On

09 Dec, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Development, Clinical Research, Protocol Development, Data Analysis, GCP Principles, Collaboration, Communication, Regulatory Compliance

Industry

Pharmaceutical Manufacturing

Description

About this role TFS HealthScience is a leading global mid size Contract Research Organization that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service capabilities, resourcing, and Functional Service solutions. The Clinical Scientist is responsible for providing scientific support to clinical development programs, contributing to the planning, execution, and interpretation of clinical studies while ensuring scientific quality and regulatory compliance. As part of our SRS FSP team, you will be dedicated to one sponsor, a global pharmaceutical or biotechnology company recognized for its innovation and commitment to advancing patient care. Approximately: 0.5 FTE Key Responsibilities • Contribute to the scientific design and implementation of clinical studies, including protocol development and study documentation • Provide scientific input throughout study start up, conduct, and closeout to ensure data quality and adherence to protocol • Review and interpret clinical data to identify trends, potential risks, and scientific insights • Collaborate with cross functional teams including clinical operations, biostatistics, data management, regulatory, and medical teams • Support preparation of clinical and regulatory documents, reports, and presentations • Ensure compliance with applicable regulations, guidelines, and internal procedures Qualifications • Advanced scientific degree in life sciences, biomedical sciences, or a related field • Experience working in clinical development or clinical research within the pharmaceutical, biotech, or CRO environment • Solid knowledge of clinical trial methodology and GCP principles • Ability to analyze and interpret complex clinical data • Strong written and verbal communication skills • Ability to work effectively in a collaborative and fast paced environment What We Offer We provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and professional growth in a rewarding environment. You will be joining a team that values collaboration, innovation, and making a difference in the lives of patients. A Bit More About Us Our journey began over 27 years ago in Sweden, in the city of Lund. As a full service, global Contract Research Organization, we build solution driven teams working towards a healthier future. Bringing together over 800 professionals, TFS delivers tailored clinical research services in more than 40 countries with flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology, Neuroscience, Oncology, and Ophthalmology. Our core values of Trust, Quality, Passion, Flexibility, and Sustainability guide decision making at all levels of the organization. They help us attract and retain talented professionals who share our values and foster a culture of collaboration, innovation, and mutual respect. Together, we make a difference.

Responsibilities

The Clinical Scientist is responsible for providing scientific support to clinical development programs and ensuring scientific quality and regulatory compliance. Key tasks include contributing to study design, reviewing clinical data, and collaborating with cross-functional teams.