Executive Clinical Development Director Hematology
- Recruiter
- Barrington James
- Location
-
United Kingdom
United KingdomUnited Kingdom
- Salary
- Competitive
- Posted
- 01 Jul 2022
- Closes
- 21 Jul 2022
- Job Title
- Associate Director
- Category
- Scientific and Pharmaceutical
- Contract Type
- Permanent
- Hours
- Full Time
We are currently looking for a Clinical Development Director who is Board Certified in Internal Medicine with at least 5 years of industry experience ( Senior and Executive levels available for more senior candidates!).
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 rare disease .
Responsibilities:
Medical Expert for clinical study team
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 with board–certification (preferably – if not then extensive experience) in Oncology / Hematology / Internal Medicine / Nephrology
Industry clinical or basic science research experience (5 years minimum)
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
Please note that this role is office–based/hybrid in Barcelona, where commute will be required.
Following your application Mollie Laurens–Chalmers, a specialist Executive Pharmaceutical Researcher, will discuss the opportunity with you in detail. She will be more than happy to answer any questions relating to the position and company, plus put a focus on career growth. The conversation can also progress further to discussing other opportunities, which are also available right now or will be imminently becoming available on the Medical Team here at Barrington James.
This position has been highly popular, and it is likely that it will close prematurely. We recommend applying as soon as possible to avoid disappointment.
Please click apply or contact Mollie Laurens–Chalmers for any further information
Mollie Laurens–Chalmers
Medical Recruitment Resourcer
Email: MLChalmers (at)
Call
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 rare disease .
Responsibilities:
Medical Expert for clinical study team
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 with board–certification (preferably – if not then extensive experience) in Oncology / Hematology / Internal Medicine / Nephrology
Industry clinical or basic science research experience (5 years minimum)
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
Please note that this role is office–based/hybrid in Barcelona, where commute will be required.
Following your application Mollie Laurens–Chalmers, a specialist Executive Pharmaceutical Researcher, will discuss the opportunity with you in detail. She will be more than happy to answer any questions relating to the position and company, plus put a focus on career growth. The conversation can also progress further to discussing other opportunities, which are also available right now or will be imminently becoming available on the Medical Team here at Barrington James.
This position has been highly popular, and it is likely that it will close prematurely. We recommend applying as soon as possible to avoid disappointment.
Please click apply or contact Mollie Laurens–Chalmers for any further information
Mollie Laurens–Chalmers
Medical Recruitment Resourcer
Email: MLChalmers (at)
Call