Global Clinical Development Director

hace 3 semanas


Barcelona, España Barrington James A tiempo completo

Barcelona
- 02-08-2023
- JOB TYPE
- Permanent
- EMP TYPE
- Full-Time
- EXPERTISE
- Business Services, Clinical Development
- SALARY TYPE
- Annually
- SALARY
- Negotiable

We are partnered with an internationally renowned pharmaceutical company who are currently looking for a Clinical Development Director with at least 5 years of industry experience (pharma/biotech).

They are looking for a Clinical Development professional to report into the VP of Clinical Development and lead the strategy, design, monitoring, data interpretation and reporting of phase II/III clinical trials of Immunology agents (including biologics). This is a fantastic opportunity in Barcelona for a medic who is passionate about clinical development to join a driven team, with plenty of progression opportunities worldwide to develop novel science.

You will serve as a medical expert for the study team and medical monitor for Phase 2-4 clinical trials. This position additionally offers substantial opportunities for regulatory and commercial interactions and career advancement in the fast-moving area of Immunology.

**Responsibilities**:

- Medical Expert for clinical study team
- Medical monitoring responsibilities
- Protocol development from concept to final protocol
- Protocol execution including interaction with investigators, and contributing to data review, data analysis and clinical study report authoring
- Strategic guidance to Phase II/III development programs and oversight of global clinical trials/trial team (s) on assigned program(s)
- Presentation at academic congresses, investigator meetings and advisory meetings
- Development of medical content for regulatory document, and responses (including but not limited to NDAs/BLAs, sNDAs/SBLAs, briefing packages and common technical documents
- Data review

**Requirements**:

- MD/MBBS/MBChB
- 5+ years of experience in the pharmaceutical industry in clinical development
- Previous clinical trial experience as medical monitor in industry setting
- Protocol development experience
- Understanding of regulatory requirements related to clinical trials
- Excellent written / oral communication skills in English
- Interest in career progression and ability to take on a more senior roles in 1-3 years
- EU citizen able to relocate to Barcelona, Spain

This is a hybrid role where you need to be based in Spain, and commute to the Barcelona office 1-2 times per week.

This position has been highly popular, and it is likely that it will close prematurely. We recommend ing as soon as possible to avoid disappointment.

Please click ‘’ or contact Mollie Laurens-Chalmers for any further information.

LI-ML1

Consultant
- Mollie Laurens-Chalmers
- +441293776644



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