Clinical Scientist

Discera Search; Dortmund; Hybrid; EUR 60.000 - 80.000; Vollzeit

Zusammenfassung

An international biotech firm is seeking a Clinical Scientist to support pivotal oncology trials. You will review clinical study data, develop analytical tools, and coordinate with internal teams. Ideal candidates will have clinical development experience and a passion for data. The position is largely remote with some in-person requirements in Germany, offering a supportive work culture and emphasis on work-life balance.

Leistungen

Supportive work culture

Emphasis on work-life balance

Flexible in-office presence after initial months

Qualifikationen

• Experience in Clinical Development with an oncology background.
• Strong understanding of trial processes and literature.
• Fluent in English (German not required).

Aufgaben

• Review TLFs and SAPs for clinical studies.
• Develop internal analytical tools for data evaluation.
• Coordinate calls with internal stakeholders for data alignment.
• Collect, analyze, and report clinical study data.
• Manage published materials for various clinical studies.
• Contribute to development of regulatory documents.
• Support internal and external meetings.
• Perform quality control on clinical documents.

Kenntnisse

Data analysis

Clinical development

Leadership feedback

Oncology expertise

Proactive attitude

Jobbeschreibung

Clinical Scientist - Germany - Remote

Location : Remote (Germany).

Title : Clinical Scientist - Reporting to Chief Development Officer.

Summary

Company Overview : Currently working with an international biotech with 1x Pivotal Phase III and 2x Phase I / II Oncology studies, seeking a DATA-DRIVEN clinical scientist.

If you love clinical development, data, and cancer research more than your own family - please read on. (Ok... close second is also fine).

The role : With a pivotal phase III top-line data readout expected by early 2027, it is critical to have the right clinical strategy and data interpretation. The Chief Development Officer relies on his CRS to analyze, review, and confirm data, study amendments, and publications. We are looking for someone who loves data, is proactive, enjoys teamwork, and wants to be part of a potential drug approval. Below are the responsibilities and requirements:

Key Responsibilities :

• Review of TLFs and SAPs of clinical studies as assigned, as the main internal stakeholder.
• Development of internal analytical tools, e.g., tumor evaluation tracker across clinical studies.
• Coordinate data alignment calls with internal stakeholders like data management, medical, stats, lab, etc.
• Collect, interpret, analyze, and report data, identifying patterns and trends.
• Manage externally published materials (posters, abstracts, manuscripts, articles).
• Contribute to development of clinical, medical, and regulatory core documents (e.g., Investigator Brochure, trial protocol, amendments, patient info, case report forms, SOPs).
• Support internal and external meetings, such as investigator meetings and data review sessions.
• Perform quality control checks of clinical, medical, and regulatory documents.

Requirements :

• Love data and confident in interpreting and acting on it.
• Experience in Clinical Development, including protocol development, data interpretation, and feedback to leadership.
• Relevant experience in Clin Ops, Medical Writing, or Data Management, especially with sponsor experience and oncology background.
• Strong oncology clinical trial experience, confident with literature and trial processes.
• Fluent in English (German not required).
• Must reside in Germany and be able to work locally; relocation is not available.
• Proactive attitude; comfortable asking questions and seeking clarification.
• Biotech experience is a plus but not essential.

The offer :

• Location: Germany. Initial 2 months require biweekly office presence; thereafter 1-3 days/month in the office.
• Company stage: Building data and presentations for multiple trials, including a global pivotal oncology trial over the next 2 years.
• Culture: Supportive, respectful, and healthy environment with great leadership.
• Holidays: Emphasis on work-life balance, personal time, and family without micromanagement.

Next Steps :

• Apply, email, or connect on LinkedIn (reference this role).
• Speak with Charles / Recruiter.
• First interview with hiring manager or team member.
• Second interview with team members.
• Final interview in person, including a brief presentation and informal meeting.
• Receive an offer.

If you want to work with a caring company on exciting data and clinical trials, apply now!

Note: I read all applications but cannot always send personal rejections. I appreciate your understanding and will provide updates on your application status.