About this role
Role Overview
- Collaborate with medical directors, scientists, regulatory professionals, biostatisticians, and others in a matrix environment to develop and execute phase 1-3 clinical trials
- Ensure high quality protocol development aligned with the Clinical Development Plan to determine a medicine’s efficacy, safety profile, and value to patients in a timely manner.
- Use medical expertise in the entire process from protocol concept to final study report to ensure scientific integrity and timely delivery of clinical trials
- Interpret and summarize study results to define safety, efficacy, and applicability of data to the targeted patient population.
- Assume medical responsibility for clinical trials with participation in real-time medical monitoring.
- Author clinical study reports and regulatory documents and respond to health authority and ethics committee queries.
- Collaborate with Principal Investigators in evaluating publications associated with clinical data.
- Network to develop strategic partnerships with thought leaders to support GSK’s vision.
Requirements
- Medical degree with board certification/eligibility or registration qualifications in medical oncology, hematology, hematology/oncology, general surgery, internal medicine, or pathology.
- Oncology experience in the pharmaceutical/biotechnology industry, clinical academic medicine, or clinical medical practice settings.
- Experience in the conduct/participation of clinical trials (investigator initiated, company sponsored or cooperative group trials) and their subsequent publications
Benefits
- Annual bonus
- Eligibility to participate in share-based long term incentive program
- Health care and other insurance benefits (for employee and family)
- Retirement benefits
- Paid holidays
- Vacation
- Paid caregiver/parental and medical leave