Medical Director / Senior Medical Director (Walpole)
Our clinical-stage biopharmaceutical client is seeking a Medical Director / Senior Medical Director with strong Oncology Clinical Development experience to cover development programs spanning phases I,II,III.
Responsibilities:
clinical leadership; from early-stage clinical trial design for novel cancer drugs through to CoP stage closely and liaise with the clinical operations team, clinical study teams, pharmacovigilance, the SVP and stakeholders in protocol design through all phases highest ethical standards are met in terms of compliance, laws and Support regulatory leaders with submissions and strategy development.
Prepare clinical reports and publications Presentations at regulatory meetings, internal and external meetings As well as the above teams, maintain and develop relationships with partners, sponsors, CROs, KOLs, and patient advocacy groups Requirements & Qualifications An M.
D.
or M.
D/Ph.
D.
with 3
years experience as a Medical Director in Oncology Clinical Development Significant drug development experience from IND through NDA Knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical trials, and experience in strategy development and protocol design Experience designing, planning, and monitoring clinical trials.
Experience presenting to internal and external audiences Ability to work well with others and build up members of a cross- functional team in a fast-paced environment #J-18808-Ljbffr Recommended Skills Clinical Development Clinical Works Drug Development Ethics Leadership Oncology Apply to this job.
Think you're the perfect candidate? Apply on company site Estimated Salary: $20 to $28 per hour based on qualifications.
Responsibilities:
clinical leadership; from early-stage clinical trial design for novel cancer drugs through to CoP stage closely and liaise with the clinical operations team, clinical study teams, pharmacovigilance, the SVP and stakeholders in protocol design through all phases highest ethical standards are met in terms of compliance, laws and Support regulatory leaders with submissions and strategy development.
Prepare clinical reports and publications Presentations at regulatory meetings, internal and external meetings As well as the above teams, maintain and develop relationships with partners, sponsors, CROs, KOLs, and patient advocacy groups Requirements & Qualifications An M.
D.
or M.
D/Ph.
D.
with 3
years experience as a Medical Director in Oncology Clinical Development Significant drug development experience from IND through NDA Knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical trials, and experience in strategy development and protocol design Experience designing, planning, and monitoring clinical trials.
Experience presenting to internal and external audiences Ability to work well with others and build up members of a cross- functional team in a fast-paced environment #J-18808-Ljbffr Recommended Skills Clinical Development Clinical Works Drug Development Ethics Leadership Oncology Apply to this job.
Think you're the perfect candidate? Apply on company site Estimated Salary: $20 to $28 per hour based on qualifications.
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