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An early stage oncology biotech is looking for a scientist or clinical project manager to help design and develop first-in-man studies.
You will be responsible for translational and phase 0/I studies working with the head of research and the head of clinical development. You will be help bring treatments into the clinical world for the first time and have access to all areas of the business.
On top of this, possibility of hybrid role (in Germany) if needed.
See below for the responsibilities, experiences required and the benefits.
As a Clinical Scientist you will be responsible for;
*Designing protocols and clinical plans using a strategic focus based on knowledge of asset, disease area, drug interactions and relevant science in order to meet requirements.
*Work with the pharmacology research team to support the preclinical dossier of bispecific antibody-based therapeutic molecules in cancer.
*Work on preclinical data generation, interpretation, and communication
*Contribute to the writing of non-clinical pharmacology study reports, investigator brochures, IND applications, regulatory annual reports, and other regulatory documents when appropriate.
*Investigator experience or knowledge is welcome as this role will interact with investigators and support when appropriate.
*Use a scientific and critical mind to medically review data of the trial, including eligibility review and safety.
*Collaborate closely with the C-level in the execution of oncology clinical trials. Participate in drafting clinical protocol synopses, clinical protocols.
The ideal Clinical / Translational Scientist will have the following skill set:
*Scientific Education (ideally Ph.D but can be bachelors / masters).
*Be able to work in Germany, EU.
*Clinical Science background( ideally Oncology but not necessary )
*Must have Clinical experiences.
*Experience with most of the points listed in the responsibilities.
*Excellent verbal and written skills.
*English fluent.
Benefits for this position:
*Base: Competitive
*Opportunity for those looking to work in Clinical Science / Development to get in (you don't need extensive study protocol development, just clinical project management).
*Hybrid work if desired.
*Supportive team and highly passionate about curing cancer.
*Help bring modern, cancer curing products, into the clinics for the 1st time.
*Learn from Chief Medical Officer and Head of Research.
*Gym, child care and relocation support if needed.
*Free fruit, tea and coffee.
Would you like to learn more? Please apply via Linkedin or reach out to me directly, all applications are confidential (tihana.sujica@epmscientific.com).
Not sure you have enough experience? Not sure if this is senior enough or challenging enough? Not sure about a career move right now?
Reach out anyway, we can have a 15 minute call and decide together if it makes sense to proceed. If this role isn't right, I have many other openings.
Clinical Scientist, Munich m/f/d
- Location Munich
- Job type Permanent
- Salary bonus
- Discipline Clinical Development
- Reference PR/356571_1653057315
You will be responsible for translational and phase 0/I studies working with the head of research and the head of clinical development. You will be help bring treatments into the clinical world for the first time and have access to all areas of the business.
On top of this, possibility of hybrid role (in Germany) if needed.
See below for the responsibilities, experiences required and the benefits.
As a Clinical Scientist you will be responsible for;
*Designing protocols and clinical plans using a strategic focus based on knowledge of asset, disease area, drug interactions and relevant science in order to meet requirements.
*Work with the pharmacology research team to support the preclinical dossier of bispecific antibody-based therapeutic molecules in cancer.
*Work on preclinical data generation, interpretation, and communication
*Contribute to the writing of non-clinical pharmacology study reports, investigator brochures, IND applications, regulatory annual reports, and other regulatory documents when appropriate.
*Investigator experience or knowledge is welcome as this role will interact with investigators and support when appropriate.
*Use a scientific and critical mind to medically review data of the trial, including eligibility review and safety.
*Collaborate closely with the C-level in the execution of oncology clinical trials. Participate in drafting clinical protocol synopses, clinical protocols.
The ideal Clinical / Translational Scientist will have the following skill set:
*Scientific Education (ideally Ph.D but can be bachelors / masters).
*Be able to work in Germany, EU.
*Clinical Science background( ideally Oncology but not necessary )
*Must have Clinical experiences.
*Experience with most of the points listed in the responsibilities.
*Excellent verbal and written skills.
*English fluent.
Benefits for this position:
*Base: Competitive
*Opportunity for those looking to work in Clinical Science / Development to get in (you don't need extensive study protocol development, just clinical project management).
*Hybrid work if desired.
*Supportive team and highly passionate about curing cancer.
*Help bring modern, cancer curing products, into the clinics for the 1st time.
*Learn from Chief Medical Officer and Head of Research.
*Gym, child care and relocation support if needed.
*Free fruit, tea and coffee.
Would you like to learn more? Please apply via Linkedin or reach out to me directly, all applications are confidential (tihana.sujica@epmscientific.com).
Not sure you have enough experience? Not sure if this is senior enough or challenging enough? Not sure about a career move right now?
Reach out anyway, we can have a 15 minute call and decide together if it makes sense to proceed. If this role isn't right, I have many other openings.