Clinical Scientist

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

Zusammenfassung

A leading biotech firm is seeking a Clinical Scientist to work on pivotal oncology clinical trials. The candidate will analyze clinical data, contribute to study documents, and ensure quality control. A passion for data and experience in Clinical Development is essential. This role allows for remote work after an initial office presence, emphasizing work-life balance and a supportive company culture.

Leistungen

Work-life balance emphasis

Supportive culture

Flexible work arrangements

Qualifikationen

• Experience in Clinical Development, particularly in Oncology.
• Fluent in English; knowledge of German is not required.
• Biotech experience is a plus.

Aufgaben

• Serve as the main internal stakeholder for clinical studies.
• Develop analytical tools for tumor evaluation.
• Coordinate data alignment calls with stakeholders.
• Analyze and report data, identifying patterns.
• Manage external publications related to clinical studies.
• Contribute to core clinical and regulatory documents.
• Support internal and external meetings and quality checks.

Kenntnisse

Data interpretation

Analytical skills

Communication skills

Proactive mindset

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, having the right clinical strategy and data interpretation is critical. The Chief Development Officer relies on his CRS to analyze, review, and confirm data, study amendments, and publications. Therefore, I am looking for someone passionate about data, proactive, team-oriented, and eager to contribute to a potential drug approval. Below are the responsibilities and what I need from you:

Key Responsibilities :

• Serve as the main internal stakeholder for review of TLFs and SAPs of assigned clinical studies.
• Develop internal analytical tools, e.g., tumor evaluation trackers across studies.
• Coordinate data alignment calls with internal stakeholders such as data management, medical, stats, lab, etc.
• Collect, interpret, analyze, and report data, identifying patterns and trends.
• Manage external publications like posters, abstracts, manuscripts, and 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 (investigator meetings, data review, advisory boards).
• Perform quality control checks on clinical, medical, and regulatory documents.

Requirements :

• Love data and confident in reading, interpreting, and acting on it.
• Experience in Clinical Development, including protocol development, data interpretation, and feedback to leadership.
• Experience in Oncology clinical trials, academic, industry, or other, with confidence in oncology literature.
• Fluent in English (German not required).
• Must reside in Germany and be able to work locally (no relocation).
• Proactive, inquisitive, and communicative.
• Biotech experience is a plus but not essential.

The offer :

• Location: Germany. First 2 months require biweekly office presence; afterward, 1-3 days/month.
• Company stage: Building data and presentations for multiple trials, including a global pivotal oncology trial.
• Culture: Supportive, respectful, and honest leadership.
• Holidays: Emphasis on work-life balance, personal time, and family.

Next Steps :

• Apply, email, or connect on LinkedIn with a note referencing this role.
• Discuss with Charles / Recruiter.
• First interview with hiring manager or team member.
• Second interview with team members.
• In-person interview with presentation and coffee.
• Receive an offer.

If you want to work with a caring company on meaningful projects in oncology, apply now! Note: I personally review all applications but may not send personal rejections. I appreciate all applicants and will provide updates on your application status.