CSL

Director, Global Clinical Scientist Lead

CSL

full-time

Posted on:

Location Type: Hybrid

Location: King of PrussiaMassachusettsPennsylvaniaUnited States

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About the role

  • Provides strategic and tactical scientific leadership and guidance for clinical development activities for 8-10 clinical scientists
  • Ensures consistency of program strategy and provides appropriate oversight and scientific support of clinical scientist activities for Phase 1-4 clinical studies
  • Collaborates with other Clinical Scientist Leads, Global Clinical Leads (GCL)s, Clinical Program Strategy (PST) representatives, and Global Product Leads (GPLs) to ensure adequate resourcing across the portfolio
  • Ensures that resourcing is adequate to cover all roles and responsibilities of the clinical scientists in the TA
  • Drives quality scientific and operational clinical development execution
  • Participates in the hiring, on-boarding, training and mentoring of Clinical Scientists
  • Accountable for providing guidance, training and mentorship to the scientist group
  • Ensures group budget is adequately planned for, communicated and tracked in accordance with CSL processes and policies
  • Provides high quality clinical & scientific content into the core clinical development documentation.

Requirements

  • Bachelor’s degree, or equivalent in Science related field is required
  • An advanced degree (MSc, PhD) in Science, PMP certification, or equivalent is preferred
  • At least 10 years of experience in the biotechnology or pharmaceutical industry (or where relevant a biomedical research organization) is required
  • Recognition and achievements in clinical sciences, document authorship, product research, process development/improvement is required
  • Has demonstrated an advanced ability and level of experience with working across multiple studies for incorporation of consistent medical/scientific concepts in multiple protocols and ensuring they meet strategic program objectives
  • Demonstrated in-depth understanding of the drug development process
  • Experience providing oversight to CROs.
Benefits
  • Health insurance
  • Professional development opportunities
  • Flexible working hours
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
clinical developmentclinical studiesscientific leadershipclinical documentationdrug development processoversight of CROsclinical scientist trainingprocess developmentmentorshipbudget planning
Soft Skills
collaborationstrategic thinkingtactical leadershipcommunicationmentoringoversightteam managementproblem-solvingorganizational skillsquality assurance
Certifications
PMP certificationMScPhD