EXPIRED – Clinical Development Medical Director / no-398

Location
CH-Basel
Start
02.05.2023
End
31.10.2023
Workload
100 %
All-in / Hour
see job description
Total Hours
1.048

Deadline:

Deadline
EXPIRED

 

EXPIRED – Clinical Development Medical Director / no-398

Location
CH-Basel
Workload
100 %

Start

02.05.2023

End

31.10.2023

DEADLINE

Deadline
EXPIRED

  • CH-Basel
  • Applications have closed
  • CH-Basel02.05.202331.10.2023100 % 1.048see job descriptionDeadline
    EXPIRED

For our customer located in Basel/Switzerland we are currently looking for a: Clinical Development Medical Director (m/f/d)

 

  • Location: CH-Basel
  • Branch: Pharma
  • Duration: 02.05.2023 – 31.10.2023
  • Pay rate: 84,51 – 105,63 chf/h

Tasks & Responsibilities

• with Significant clinical development experience is also absolutely key
• Providing clinical leadership and strategic medical input for all clinical deliverables in the assigned project or section of a clinical program
• Leading development of clinical sections of trial and program level regulatory documents
• Driving execution of the assigned clinical program and/or clinical trial in partnership with global line functions, assigned Global Trial Directors (GTDs), and regional/country medical associates, where applicable
• Supporting (Senior) Global Program Clinical Head (GPCH) in ensuring overall safety of the molecule for the assigned section, and may act as a core member of the Safety Management Team (SMT), supporting overall program safety reporting in collaboration with Patient Safety colleagues
• Supporting the Clinical Development Head (CDH) by providing medical input into Clinical Development Plan (CDP), Integrated Development Plan (IDP) and Clinical Trial Protocol (CTP) reviews, and contributing to/driving development of disease clinical standards for new disease areas
• As a medical expert, supporting the (Sr.) GPCH or CDH in interactions with external and internal stakeholders and decision boards
• May work with a  Institute of Biomedical Research/ Translational Medical Sciences to drive transition of pre-PoC (Proof of Concept) projects to DDP (Development Decision Point) and with BD&L (Business Development & Licensing) including target identification and due diligences together with other medical matters, as needed.

Must Haves

  • MD or equivalent medical degree is required in addition to advanced knowledge and clinical training in medical/scientific area; Clinical practice experience 4 years (including residency) and board certification
  • Minimum of 7 years of experience in clinical research or drug development
  • Experience in an academic clinical research or industry environment spanning clinical activities in Phases I through IV required.
  • 2 years of 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 required.
  • Working knowledge of disease area is required, with proven ability to interpret, discuss and present efficacy and safety data relating to clinical trial(s) and proven ability to understand and interpret basic and clinical scientific research reports
  • Demonstrated ability to establish effective scientific partnerships with key stakeholders
  • Working knowledge of GCP, clinical trial design, statistics, and regulatory and clinical development processes
  • Previous global people management experience is preferred, though this may include management in a matrix environment.

Did we catch your interest?

The SimplyVision-Team is looking forward to receive your application (Word file is highly appreciated).

Kindly be informed that our customer is located in Switzerland. Therefore only applications from candidates within the EU or candidates holding Swiss work permission are required.

  • CH-Basel
  • Applications have closed
  • CH-Basel02.05.202331.10.2023100 % 1.048see job descriptionDeadline
    EXPIRED

For our customer located in Basel/Switzerland we are currently looking for a: Clinical Development Medical Director (m/f/d)

 

  • Location: CH-Basel
  • Branch: Pharma
  • Duration: 02.05.2023 – 31.10.2023
  • Pay rate: 84,51 – 105,63 chf/h

Tasks & Responsibilities

• with Significant clinical development experience is also absolutely key
• Providing clinical leadership and strategic medical input for all clinical deliverables in the assigned project or section of a clinical program
• Leading development of clinical sections of trial and program level regulatory documents
• Driving execution of the assigned clinical program and/or clinical trial in partnership with global line functions, assigned Global Trial Directors (GTDs), and regional/country medical associates, where applicable
• Supporting (Senior) Global Program Clinical Head (GPCH) in ensuring overall safety of the molecule for the assigned section, and may act as a core member of the Safety Management Team (SMT), supporting overall program safety reporting in collaboration with Patient Safety colleagues
• Supporting the Clinical Development Head (CDH) by providing medical input into Clinical Development Plan (CDP), Integrated Development Plan (IDP) and Clinical Trial Protocol (CTP) reviews, and contributing to/driving development of disease clinical standards for new disease areas
• As a medical expert, supporting the (Sr.) GPCH or CDH in interactions with external and internal stakeholders and decision boards
• May work with a  Institute of Biomedical Research/ Translational Medical Sciences to drive transition of pre-PoC (Proof of Concept) projects to DDP (Development Decision Point) and with BD&L (Business Development & Licensing) including target identification and due diligences together with other medical matters, as needed.

Must Haves

  • MD or equivalent medical degree is required in addition to advanced knowledge and clinical training in medical/scientific area; Clinical practice experience 4 years (including residency) and board certification
  • Minimum of 7 years of experience in clinical research or drug development
  • Experience in an academic clinical research or industry environment spanning clinical activities in Phases I through IV required.
  • 2 years of 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 required.
  • Working knowledge of disease area is required, with proven ability to interpret, discuss and present efficacy and safety data relating to clinical trial(s) and proven ability to understand and interpret basic and clinical scientific research reports
  • Demonstrated ability to establish effective scientific partnerships with key stakeholders
  • Working knowledge of GCP, clinical trial design, statistics, and regulatory and clinical development processes
  • Previous global people management experience is preferred, though this may include management in a matrix environment.

Did we catch your interest?

The SimplyVision-Team is looking forward to receive your application (Word file is highly appreciated).

Kindly be informed that our customer is located in Switzerland. Therefore only applications from candidates within the EU or candidates holding Swiss work permission are required.

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