Clinical Development Director

Clinical Development Director

18 month Contract
Hybrid or remote

Job Purpose
The Clinical Development Director (CDD) is the clinical/scientific and clinical development expert and provides leadership and support to clinical development deliverables and activities within a defined global clinical development program and/or global clinical trial (e.g. clinical development plan, clinical trial protocol), under the
leadership of the GPCH.

Major Activities

1. Supports and if assigned leads delivery of all assigned clinical deliverables in the assigned section of a clinical program. Clinical deliverables may include the clinical development strategy for assigned program section(s), clinical sections of individual protocols consistent with the Integrated Development Plans (IDP), clinical data review and program specific standards, clinical components of regulatory documents/registration dossiers, and publications
   
2. Provides input into final analyses and interpretation including the development of the Clinical Study Report(s) (CSRs), publications and internal/external presentations.
   
3. 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)
   
4. Oversees/conducts ongoing clinical and scientific review of clinical trial data with medical monitor, Clinical Scientific Expert(s) with appropriate oversight from Medical Lead. Work in close collaboration with the data management and statistics teams to ensure proper data quality and analysis of clinical trial results.
   
5. Inspection Readiness and interaction with QA - risk assessments, audit preparation, mock interviews, storyboard and presentation prep; Author and/or review abstracts, presentations and manuscripts for accuracy of clinical data and content
   
6. May be the Program Manager of other associates (e.g., CSE)
   
7. Provides support to Sr CDMD and/or GPCH in monitoring and safety data and signals the molecule for the assigned section of the clinical trial, may be a 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 the medical monitor, CDMD and Patient Safety Major Activities CDD
   
8. As a clinical development expert, may support the GPCH or CDH 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
   
9. May work with 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 assigned
   
10. Ensures career development of Program reports and other clinical colleagues through active participation in the performance management and talent planning processes. Provides on-boarding, training, & mentoring support
    
11. Contributes to medical/scientific training of relevant Client's stakeholders on the disease area and compound/molecule. May serve as speaker for franchise medical/scientific training
    
12. May serve on or lead global initiatives (e.g., process improvement, training, SOP development, other Clinical Development line function initiatives)
    
13. May be assigned to lead clinical trial(s) as Clinical Scientific Lead and provide leadership and guidance for all clinical aspects of a clinical trial in close collaboration with the assigned medical monitor and/or CDMD
    
    KPI's
    

• Timely delivery of high quality IDP/CDP sections, CTPs, and other clinical deliverables aligned with IDP/CDP and TPP and endorsed by review committees and internal boards, with acceptance by key external and internal stakeholders
  
• Applies effective clinical research methodology, including trial /analyses, efficacy endpoints, safety assessments, and risk management across disease
  area and development phases
  
• Strong evidence of quality clinical/scientific review of trial data; lead TA through high quality IDP and protocol reviews; timely development of quality disease/program clinical standards, publications, internal/external presentations, and other CD deliverables
  
• Strong evidence of quality contributions to and acceptance of clinical sections of
  regulatory documents, Investigators' Brochures, briefing books, safety updates,
  and submission dossiers by key external and internal stakeholders
  
• Well managed, effective, and engaged clinical teams; demonstrated ability to
  deputize for GPCH at GCT, as well as other venues as needed
  
• Clearly demonstrates Client Values and Behaviours
  
  Number of associates: May lead team of approx. 3 direct and indirect reports (dependent on the size of the programs and functional responsibilities)
  Financial responsibility: Overall lifetime clinical budget of program which can vary and be in excess of $20 million.
  
  Impact on the organization:
  External
  
• Timely submission and delivery of high-quality clinical program data supporting regulatory approval of key compounds (or new indications), as appropriate
  
• Effective interaction with and influence on key external decision makers (e.g., regulatory authorities, medical experts, pricing and reimbursement bodies)
  Internal
  
• Clinically and scientifically sound programs and trials resulting in the timely delivery of
  high-quality data and analysis of trial data which enables strategic decisions within the clinical program
  
• High quality clinical/scientific review of CTPs and CDPs, industry leading clinical processes
  
• Identification and development of key talent
  
  Ideal Background
  Experience/Professional requirement:
  
• ≥ 7 years of involvement in clinical research or drug development in an academic or industry environment spanning clinical
  activities in Phases I through IV. ≥ 3 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
  
• Advanced knowledge of assigned therapeutic area
  
• Demonstrated ability to establish strong scientific partnership with key stakeholders
  
• Thorough knowledge of GCP, clinical trial design and methodology, statistical analysis
  methodology, and regulatory/clinical development process
  
• Around 1 year of People management experience preferred this may include
  management in a matrix environment. Global people management experience
  desirable
  
• Excellent communication skills, written and oral
  
• Excellent interpersonal skills
  
• Excellent negotiation and conflict resolution skills
  
  Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy