Clinical Development Medical Director - Breast Cancer (m/f/d)

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Beschreibung



Clinical Development Medical Director - Breast Cancer (m/f/d)

Reference: -en
Start: asap
Duration: 20 MM++

Main tasks:
  • Provides clinical leadership and medical strategic input for all clinical deliverables in the assigned project or section of a clinical program if applicable. Clinical deliverables may include clinical sections of individual protocols consistent with the Integrated Development Plans (IDP), clinical data review, program specific standards, clinical components of regulatory documents/registration dossiers, and publications
  • Leads development of clinical sections of trial and program level regulatory documents (e.g., Investigator’s Brochures, briefing books, safety updates, submission dossiers, and responses to Health Authorities)
  • Drives execution of the section of the clinical program in partnership with global line functions, assigned Global Trial Directors (GTDs), and regional/country medical associates if applicable
  • Oversees/conducts ongoing medical and scientific review of clinical trial data with Clincal Scientific Expert(s)
  • May be the Program Manager of other associates (e.g.., CSE)
  • May act as study medical monitor 
  • Supports (Sr.) GPCH in ensuring overall safety of the molecule for the assigned section, may be a core member of the Safety Management Team (SMT), and supports overall program safety reporting (e.g., Periodic Safety Update Reports (PSURs), Drug Safety Update Reports (DSURs), and other safety related documents) in collaboration with Patient Safety
  • Supports the Therapeutic Area Head (TAH) by providing medical input into IDP and CTP reviews and contributing/driving development of disease clinical standards for new disease areas. May take on other TA responsibilities as directed by the TAH
  • As a medical expert, supports the (Sr.) GPCH or TAH in interactions with external stakeholders (e.g., regulatory authorities, key opinion leaders, data monitoring boards, advisory boards, patient advocacy groups), internal stakeholders (e.g., CTT, Research, Translational Medicine, Global Medical Affairs, Marketing, HE&OR), and internal decision boards


Main qualifications
  • MD or equivalent medical degree required
  • Advanced knowledge and clinical training in a medical/scientific area (e.g., internal medicine or sub-specialty) required, with Medical Board certification preferred
  • Profound Clinical practice  (including residency) preferred
  • Previous involvement in clinical research or drug development in an academic or industry environment spanning clinical activities in Phases I through IV
  • Previous contribution to and accomplishment in all aspects of conducting clinical trials (e.g., planning, executing, reporting and publishing) in a global/matrix environment in pharmaceutical industry
  • Experience with Breast Cancer
  • Profound experience as a clinical research physician in the pharma/biotech industry with oncology solid tumor (lung cancer, preferred) 
  • Demonstrated ability to establish strong scientific partnership with key stakeholders
  • Thorough knowledge of GCP, clinical trial design, statistical analysis methodology, and regulatory/ clinical development process
  • People management experience preferred, this may include management in a matrix environment. Global people management experience desirable
  • Excellent communication skills, written and oral  


Main advantages:
  • You will work in an international environment



About us:
With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.

My contact at Hays:

My contact person:
Emina Mustafic

Referencenumber:


Make contact:
Phone:
Email:
Start
ab sofort
Dauer
20 MM++
(Verlängerung möglich)
Von
Hays AG
Eingestellt
23.01.2021
Ansprechpartner:
Kerstin Werner
Projekt-ID:
2034724
Vertragsart
Freiberuflich
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