Remote Clinical Research Associate Job at TFS HealthScience, Germany | Life Sciences Candidate, Apply Online
Looking for a clinical research associate job in Germany? TFS HealthScience is seeking a Clinical Research Associate (m/f/d) to join its Clinical Development Services (CDS) Oncology team. This full-time, home-based opportunity is suited to candidates with clinical research experience or relevant academic knowledge who want to contribute to clinical trials, patient safety, and oncology research.
- Position: Clinical Research Associate (m/f/d)
- Department: Clinical Development Services (CDS) – Oncology
- Location: Berlin, Germany
- Work Arrangement: Fully remote / home-based
- Job Requisition ID: 599264
About The Company
TFS HealthScience is a global Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout the clinical development process. Founded in Lund, Sweden, the company provides full-service clinical research, functional service provision (FSP), and resourcing solutions across therapeutic areas including oncology, dermatology, neuroscience, and ophthalmology.
With a team of more than 600 professionals and operations across over 50 countries, TFS focuses on delivering quality clinical research through collaboration, innovation, and patient-centered practices.
Job Description
TFS HealthScience is hiring a Clinical Research Associate (m/f/d) for its CDS Oncology team, with the position based remotely in Germany. Candidates in the Hamburg area are preferred.
The selected candidate will work as part of a clinical project team, supporting the initiation, monitoring, and closeout of clinical trial sites. The role involves ensuring compliance with study protocols, company procedures, Good Clinical Practice (GCP), International Council for Harmonisation (ICH) guidelines, and applicable regulatory requirements.
Remote Clinical Research Associate Job – Key Responsibilities
- Conduct onsite and remote monitoring of clinical trials in accordance with sponsor requirements, standard operating procedures, GCP, ICH guidelines, and relevant regulations.
- Ensure participant safety, data integrity, and clinical trial quality through monitoring activities.
- Verify informed consent procedures and compliance with study protocols.
- Review electronic or paper case report forms (CRFs) and source documentation for accuracy and validity.
- Check the proper handling, management, and accountability of investigational products.
- Prepare monitoring visit reports, document findings, track corrective and preventive actions, and escalate issues when necessary.
- Communicate identified issues and required action items to clinical trial sites.
- Submit essential site documents to the electronic Trial Master File (eTMF) or paper Trial Master File (TMF).
- Verify that Investigator Site Files (ISFs) are maintained according to GCP, ICH guidelines, and local regulatory requirements.
- Support audit and inspection preparation, participation, and follow-up activities.
- Coordinate clinical investigative supplies, including ordering, shipping, and reconciliation where applicable.
- Maintain accurate site-level information in Clinical Trial Management Systems (CTMS) and other project-related systems.
Educational Requirements For Remote Clinical Research Associate Job
- Bachelor’s degree, preferably in Life Sciences or an equivalent qualification.
- More than one year of relevant clinical experience or a relevant academic background in clinical trials or clinical development activities.
Skills and Qualifications
- Understanding of Good Clinical Practice (GCP) regulations and ICH guidelines.
- Basic knowledge of medical terminology and the science related to assigned drugs and therapeutic areas.
- Strong written and verbal communication skills.
- Fluency in both English and German.
- Excellent organizational and time-management skills.
- Good computer skills and confidence using clinical research software.
- Ability to work independently and within cross-functional project teams.
- Adaptability in fast-paced environments with changing priorities.
- Strong analytical thinking, attention to detail, and a proactive approach.
- Collaborative mindset, flexibility, and sound professional judgment.
- Willingness and ability to travel approximately 60–80%, including overnight and international travel when required.
This clinical research associate job offers an opportunity to contribute to oncology clinical trials while developing expertise in site monitoring, regulatory compliance, clinical documentation, and patient safety. Candidates with relevant clinical research knowledge, strong organizational skills, and fluency in German and English can explore this opportunity with TFS HealthScience.
Questions and comments