Interventional Study Scientist Medical Director
$187.28k - $312.13kGlaxosmithkline
Interventional Study Scientist Medical DirectorLocations – GSK HQ UK, New Oxford Street & USA - Upper Providence/ Waltham MAReports to: Head of Interventional & Supported StudiesJoin GSK's Medical Affairs team and be part of a global organization that drives innovation, scientific excellence, and patient-centered solutions. At GSK, we are committed to improving lives by ensuring the safe and effective use of our medicines and vaccines, bridging critical scientific insights with impactful healthcare strategies. As a member of Medical Affairs organisation, you’ll collaborate with cross-functional teams to shape clinical practice, engage with healthcare professionals, and deliver on our promise to help people do more, feel better, and live longer.This role offers an exciting opportunity to lead the scientific design and execution of interventional clinical studies within the Medical Affairs organization. You will play a pivotal role in shaping data generation strategies, ensuring studies are conducted with the highest standards of quality and ethics, and collaborating with cross-functional teams to deliver impactful results. We are looking for a leader who is passionate about advancing science, thrives in a collaborative environment, and is motivated to make a meaningful impact on patient outcomes.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 & SkillsExperience leading global Phase IIIb/IV interventional studiesExperience 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?We are seeking candidates who want to grow into a visible scientific leader. This is a hybrid role based in either United Kingdom or United States with an expected in-office presence of around two to three days per week. You will have the opportunity to shape strategy, mentor colleagues, and influence clinical evidence generation across teams.We are committed to creating an inclusive workplace where everyone can thrive. If you are passionate about making a difference and have the skills and experience, we are looking for, we encourage you to apply.Closing Date for Applications: 7th August 2026 (EOD) Please take a copy of the Job Description, as this will not be available post closure of the advert. When applying for this role, please use the ‘cover letter’ of the online application or your CV to describe how you meet the competencies for this role, as outlined in the job requirements above. The information that you have provided in your cover letter and CV will be used to assess your application. SkillsDigital 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.Why GSK?Uniting science, technology and talent to get ahead of disease together.GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at View email address on click.appcast.io where you can also request a call.Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a Recruitment FAQ guide. Click the link where you will find answers to multiple questions we receiveImportant notice to Employment businesses/ AgenciesGSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at SummaryLocation: UK – London – New Oxford Street; USA - Massachusetts - Waltham; USA - Pennsylvania - Upper ProvidenceType: Full time
$199k - $343.85k
...currently searching for the best talent for a Medical Director Clinical Development. This is a hybrid... ...listed within the job posting.The Interventional Oncology (INTO) group, a cross-sector... ...clinical trial data. Able to manage study start-up, and guides study team in...SuggestedFull timeWork at officeLocal areaImmediate start$119.7k - $222.3k
...Location: Cambridge MA Internal: Principal Scientist I/II LI#-Hybrid The individual will... ...scientific and operational support to Study Quality and Compliance group within the... ...individuals with disabilities. If, because of a medical condition or disability, you need a...SuggestedPermanent employment$260k - $318k
...leading the fight against MASH.Madrigal’s medication, Rezdiffra (resmetirom), is a once-... ...time, in the right way.The Senior Director, Clinical Scientist, will support the development and execution... ...across clinical programs, driving study design, execution, and cross-...SuggestedMinimum wageFull timeLocal areaFlexible hours- ...our Philadelphia, PA headquarters. The Director, Clinical Scientist plays a key role in supporting the... ...of-concept through late-stage pivotal studies, working closely with Clinical Operations... ...CAR-T programs, partnering with the Medical Director and other Clinical...SuggestedRemote work
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...of the way.Learn more at The Director Clinical Research Oncology is... ...implementation of clinical research studies that are part of a global... ...with the clinical project scientists and Clinical Leader in Late Development... ...studies. He/She leads the medical review of critical data...SuggestedFull timeContract workWork experience placementImmediate start$213k - $260k
...the fight against MASH.Madrigal’s medication, Rezdiffra (resmetirom), is a once-... ...Safety & Aggregate Reporting, the Director, Global Clinical Safety Scientist will play a key role within Clinical... ...critical feedback to relevant sections of study documents including Protocol,...Minimum wageFull timeLocal areaFlexible hours$178k - $218k
...our shared purpose: leading the fight against MASH.Madrigal’s medication, Rezdiffra (resmetirom), is a once-daily, oral, liver-... ...right way.Madrigal Pharmaceuticals is seeking an Associate Director, Study Toxicologist to support nonclinical development programs for...Minimum wageFull timeContract workLocal areaFlexible hours- ...&D will serve as a clinical sciences leader on global oncology studies and contribute to program-level activities. Responsible for the... ...to-end clinical development strategy.Assume responsibility for medical review of clinical trial data, both directly as needed and/or via...Full timeContract workLocal areaRelocation
- ...execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.Job Description• The Study Specialist will augment activities performed by existing study team members whether from client or client’s preferred CROs by providing...Local areaImmediate startRemote work
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...against MASH.Madrigal’s medication, Rezdiffra (... ...Senior Medical Medical Director, Translational Medicine... ...is a senior physician-scientist responsible for leading... ...mechanistic clinical studies and shaping the... ...leadership of early phase interventional trials.· Strong track...Minimum wageFull timeLocal areaFlexible hours$203.78k - $339.63k
...and patients. The role of Director, Global Real-World Evidence... ...& Health Outcomes Research Scientist is critical to achieving this... ...evidence and other non-interventional study methods. The role will be a... ...for engaging closely with medical and matrix stakeholders and...Full timeLocal areaWork from homeFlexible hours- ...Clinical Study Manager At Real we're always looking for new and ambitious people to help deliver exceptional service levels, change... ...with some of the world's best pharmaceutical, biotechnology and medical companies. As specialists in recognising talent we pride ourselves...Local areaFlexible hours
$284.25k
The Senior Medical Director, Oncology Clinical Development - GU will report... ...with physicians, scientists, regulatory professionals,... ...develop and execute phase 1-3 interventional clinical trialsRepresent Clinical... ...(protocol concept to final study report) to ensure...Full timeWork at officeLocal areaWorldwide2 days per week$185.25k - $308.75k
...Position Summary The role of Director, Global Real-World... ...Outcomes Research Scientist Hematology-Oncology ensures... ...and execute multiple studies for a given asset and... ...internal experts (medical affairs, clinical, commercial... ...across the non-interventional study organization. Build...Local area$120 - $135 per hour
...What You'll Be Doing: This position can be part-time or full-time. Minimum 20 hours per week. As a Cardiology, Field Medical Director you will be a key member of the utilization management team. We can offer you a meaningful way to make a difference in patients...Full timePart timeWork at officeImmediate start- ...drivers of disparities is highly desired. Must-haves Evaluation science background Understanding of control/intervention groups Ability to identify and address bias in study designs Experience with patient outcomes, patient behavior measurement, or healthcare program...
- ...I. Qualifications The associate medical director shall be licensed to practice medicine in the... ...to primary physicians on medical interventions consistent with the hospice philosophy... ...or outside seminars or approved self-study and research. Documentation of orientation...
- ...'s ability to pay for health care. The Invasive Cath Lab/Interventional Radiology Technologist performs interventional radiology examinations... ...Epic Demonstrates the action of understanding specific medications utilized in Cardiac catheterization procedures and...Full time
- ...Join a cardiology practice of 2 interventional cardiologists, 1 non-invasive, 2 electrophysiologists... ...-V ICD: 65 Loop Recorder Insert: 177 EP Study: 23 Ablation simple: 171 Ablation... ...allowance annual CME stipend paid vacation medical/dental/vision and life insurance...Work at officeLocal areaRelocation packageMonday to FridayNight shiftWeekend work
- ...coronary, vascular and structural heart interventions and an advanced heart failure program.... ...through the Geisinger Center for Clinical Studies. The Institute serves as an educational... ...Medicine (Required) Experience: Licensed Medical Doctor - State of Pennsylvania Skills...Full timePart time
- ...practice. Our team comprises 2 noninvasive, 2 interventional and as well as a team of 3 advanced... ...?ll feel at home in our sophisticated medical community in the heart of Central... ...interpret laboratory tests and diagnostic studies Perform procedures as applicable to...Full timePart timeReliefWork at officeImmediate startRelocation packageFlexible hours
$123k - $130k
...feel passionate about.Job OverviewServe as the Principle Investigator/Senior Scientist responsible for the development and execution of highly complex method development and characterization studies related to the testing characterization and analysis of biotherapeutics...Contract workFor subcontractorLocal areaWorldwideFlexible hours- ...offering contingent labor as a variable cost.Job Description• The scientist will be responsible for activities that support protein... ...provide protein for high-throughput screening and crystallography studies. • Additional responsibilities include experimental design, data...Immediate start
- ...recruiting a Senior Autonomous Systems Research Scientist who has a passion for solving complex... ...performance.Collaborative Autonomy: Study AI approaches to motion planning, task planning... ...of benefits including comprehensive medical, prescription, dental, and vision insurance...Full timeWork experience placement
$156.9k - $247k
...senior leader, an Associate Principal Scientist/Associate Director, has primary responsibility for... ...and health systems globally.Types of studies executed include prospective and retrospective... ...with clinical development, medical affairs, biostatistics, market access...Full timeFor contractorsLocal areaFlexible hours$173.2k - $272.6k
...Research Laboratories, is seeking a Principal Scientist to join our department in West Point, PA... ...and drug products from preclinical studies through Phase III clinical trials with... ...of benefits. Available benefits include medical, dental, vision healthcare and other insurance...Full timeFor contractorsLocal areaFlexible hours- ...sciences and in the support of clinical studies, as well as having an emerging global presence... ...time benefits including comprehensive medical coverage, dental, and vision optionsLife... ...hire, train and manage highly qualified scientists to perform laboratory services using our...Full timeContract workDay shift
- ...Hands-on experience with operating HPLC is an added plus.Responsibilities include (1) execution of process development laboratory studies (fermentation, purification) and maintaining thorough records in lab notebooks [80% time] and (2) assisting with protocols, development...Work at officeImmediate start
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- ...of the Position:We are seeking a highly skilled and motivated Scientist with expertise in cell-based assays for CAR T cell therapy. As... ...Cabaletta Bio lab safety policies and SOPs.Oversee in vivo mouse studies and perform related ex vivo assays as needed.Ensure proper maintenance...
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