Clinical Research Coordinator managing screening, enrollment, and retention of study participants for USF. Ensuring quality of data and implementing research procedures under supervision.
About the role
- Director, Global Clinical Scientist Lead at CSL Behring overseeing clinical development activities for a team of clinical scientists. Collaborating cross-functionally to drive strategic clinical programs.
Responsibilities
- 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
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Tech skills
Location requirements
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