Clinical Scientist

Discera Search; Stuttgart; Hybrid; EUR 70.000 - 90.000; Vollzeit

Zusammenfassung

A leading international biotech company is looking for a Clinical Scientist to contribute to pivotal oncology studies. The role involves reviewing clinical data, developing analytical tools, and collaborating with stakeholders to ensure data integrity for drug approval processes. The ideal candidate is proactive, passionate about data, and has relevant clinical development experience. This position is remote with occasional office presence in Germany.

Leistungen

Emphasis on work-life balance

Supportive work culture

Opportunities for personal growth

Qualifikationen

• Experience in Clinical Development, including protocol development.
• Passion for data and confidence in interpretation.
• Oncology clinical experience is beneficial.

Aufgaben

• Review TLFs and SAPs of clinical studies.
• Develop internal analytical tools.
• Conduct data alignment calls with stakeholders.
• Perform data analysis, interpretation, and reporting.

Kenntnisse

Data analysis

Clinical development experience

Oncology experience

Proactive communication

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 company conducting pivotal and early-phase oncology studies, seeking a data-driven clinical scientist.

The role : With a pivotal phase III top-line data readout expected by early 2027, it is crucial to have the right clinical strategy and data interpretation. The Chief Development Officer relies on the CRS to analyze, review, and confirm data, study amendments, and publications. We are looking for someone passionate about data, proactive, team-oriented, and interested in contributing to potential drug approval. Responsibilities include:

• Review of TLFs and SAPs of clinical studies.
• Development of internal analytical tools, e.g., tumor evaluation trackers.
• Data alignment calls with stakeholders.
• Data analysis, interpretation, and reporting.
• Coordination of externally published materials.
• Contributing to core clinical, medical, and regulatory documents.
• Supporting meetings such as investigator meetings and data reviews.
• Quality control of documents.

Requirements :

• Love data and confident in reading and interpreting it.
• Experience in Clinical Development, including protocol development and data interpretation.
• Oncology clinical experience, in academia, industry, or other settings.
• Fluent in English (German not required).
• Based in Germany and able to work locally.
• Proactive and communicative.
• Biotech experience is a plus.

The offer :

• Location: Germany, with initial biweekly office presence, then 1-3 days/month.
• Company stage: Building data for multiple trials, including a global pivotal oncology trial.
• Culture: Supportive, respectful, and honest environment.
• Holidays: Emphasis on work-life balance and personal time.

Next Steps :

• Apply, email, or connect on LinkedIn.
• Initial interview with Charles or another recruiter.
• Team interview.
• In-person interview with presentation.
• Offer stage.

If you are passionate about data, clinical trials, and making a difference, apply now! Please note, due to volume, personal rejection notes may not be provided, but you will receive updates on your application status.