Clinical Scientist

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

Zusammenfassung

A leading biotech firm is looking for a data-driven Clinical Scientist to analyze oncology trial data. The role requires collaboration with various internal teams, data interpretation, and participation in multiple clinical studies. Excellent English and relevant oncology clinical experience are mandatory. This position allows for remote work after an initial office presence. Enjoy a supportive company culture that values both professional growth and personal time.

Leistungen

Healthy company culture

Supportive management

Flexibility for personal time

Qualifikationen

• Love data and confident in ability to read, interpret and action it.
• Clinical Development experience with protocol development or amendments.
• Confident in oncology clinical trials and literature.
• Proactive and not afraid to ask questions.

Aufgaben

• Main internal stakeholder for review of TLFs and SAPs.
• Develop internal analytical tools for clinical studies.
• Collect, interpret, analyze, and report on data.
• Coordinate externally published materials.
• Support internal and external meetings.
• Conduct quality control checks of clinical documents.

Kenntnisse

Data interpretation

Clinical development

Oncology clinical experience

Proactivity

Fluent English

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 who is looking for a DATA DRIVEN clinical scientist.

If you love clinical development, data and cancer research more than your own family - please read on. (ok.....close 2nd is also fine).

The role : With a pivotal phase III top-line data read out expected by early 2027, it is critical to have the right clinical strategy and data interpretation. The Chief Development Officer is in many meetings so he relies on his CRS to analyse, review and confirm the data, study amendments and anything that is published.Therefore I am looking for someone who loves data, is proactive, enjoys working in a team and wants to be part of a potential drug approval. Below is what you will be doing and more about what I need :

Key Responsibilities :

• Main internal stakeholder for review of TLFs and review of SAPs of clinical studies as assigned.
• Responsible for development of adequate internal analytical tools e.g. tumour evaluation tracker across clinical studies as assigned.
• Responsible for the internal data alignment call with all internal stakeholders e.g. data management, medical, stats, lab etc.
• Collect, interpret, analyse, and report on data, identifying patterns and trends in data sets.
• Responsible for coordination of externally published materials (posters, abstracts, manuscripts, and articles), as assigned.
• Contribute to the development clinical, medical, and regulatory core documents (e.g., Investigator Brochure, trial protocol, trial amendments, patient information sheet and consent form, case report forms, SOPs, and others), as assigned.
• Support various internal and external meetings, e.g., investigator meetings, data review or clinical advisory board meetings, as assigned.
• Quality control checks of clinical, medical, and regulatory documents, as assigned.

Requirements :

Essential : Love data and confident in your ability to read, interpret and action it.

Essential : Clinical Development - must have Clin Dev work - this includes areas like protocol development or amendments, interpreting data and feeding back to leadership or other areas strong related to this.

If : If you have a Clin Ops background only - it could work if you have sponsor experience and worked in oncology. The same for Medical Writing or Data Management. Those with no Clinical Development and no Sponsor experience it will be hard to progress.

Essential : Oncology clinical experience - this can be in the form of academic, industry or other but you must feel very confident in oncology clinical trials and literature.

Essential : English fluent (German not needed).

Essential : Must be in Germany and able to work here - we can not relocate people at this stage.

Essential : Proactive and not afraid to ask questions or reach out if you are unsure / if others are slowing you down.

Ideal not essential : Biotech experience.

The offer :

Location : Germany - first 2 months I need biweekly office presence (location shared after conversation). After that 1-3 days a month in the office.

Company stage : Next 2 years is building data and presentations for multiple trials including a global pivotal oncology trial.

Culture : Honest when I say this - the executive team are great people. Culture is healthy, respectful and supportive.

Holidays : Company takes seriously holiday, personal time and room for you and family - no micromanagement, get your work done and spend time with family / yourself.

Next Steps :

Apply here, send me an email or connect on Linkedin (with a note referencing this).

Talk with Charles / Recruiter.

First Interview - With hiring manager or team member.

Second Interview - with others in team.

Third interview - in person, small presentation and coffee together.

Offer.

So, if you want to work with a wonderful company that cares for its people and you personally enjoy data, clinical trials and the opportunity to work on something special - then apply now!

Note - I am a human. I read all applications but I do not have time to send personal rejection notes - dont hate me for this. I appreciate all those who apply and I try my best, at a minimum, to give a Yes / No note so you know the status of your application. )