Interventional Study Scientist Medical Director
Locations
Reports to
In this role, you will
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
- Design and oversee interventional clinical studies, ensuring alignment with strategic objectives and evidence plans.
- Facilitate medical governance, review safety data and guide risk mitigation actions.
- Provide scientific oversight for study protocols, analysis plans, and interpretation of study data.
- Ensure patient safety and scientific integrity throughout study conduct, including medical governance and monitoring.
- Collaborate with cross-functional teams to ensure seamless execution and delivery of clinical programs.
- Prepare and present study results for scientific meetings, publications, and regulatory submissions.
- Engage with internal and external stakeholders, including investigators and thought leaders, to enhance study design and execution.
Basic Qualifications & Skills
We are seeking professionals with the following required skills and qualifications to help us achieve our goals:
- Advanced degree in a relevant scientific discipline (MD, PhD, PharmD, or equivalent).
- Substantial experience leading interventional clinical studies in a therapeutic area such as oncology/haematology/ Immunology, Specialty, and other GSK-related therapeutic areas of interest.
- Considerable experience in clinical research, including interventional studies.
- Proven experience designing and executing clinical trials with demonstrated impact.
- Strong understanding of regulatory requirements and industry best practices for clinical research.
- Excellent communication and organizational skills.
Preferred Qualifications & Skills
- Experience leading global Phase IIIb/IV interventional studies
- Experience collaborating with regulatory authorities.
- Familiarity with innovative approaches in clinical trial design and execution.
- Exposure to working with key opinion leaders, investigators, and external partners.
- Experience developing scientific content for publications and regulatory submissions.
- Understanding of digital tools and methodologies for evidence generation.
- Experience leading cross-functional teams in a matrixed environment.
Why You?
Skills
Digital Fluency, Enterprise Thinking, External Stakeholder Management, High Impact Communication, Launch Excellence, Patient Impact
- If you are based in Cambridge, MA; Waltham, MA; Rockville, MD; or San Francisco, CA, the annual base salary for new hires in this position ranges $187,275 to $312,125. The US salary ranges take into account a number of factors including work location within the US market, the candidate’s skills, experience, education level and the market rate for the role. In addition, this position offers an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. Available benefits include health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave. If salary ranges are not displayed in the job posting for a specific country, the relevant compensation will be discussed during the recruitment process.
Uniting science, technology and talent to get ahead of disease together.
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Not included in the source posting: about the role, what you'll do, benefits.
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