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.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
$122k - $212.75k
...talent for a The Associate Director, Clinical Project Scientist to be based in Horsham,... ...of Investigator Initiated Study(ies) (IIS), collaborative... ...(CSS), including both interventional and registry studies. In... ...in collaboration with US Medical Affairs Oncology staff as...SuggestedFull timeContract workTemporary workLocal areaFlexible hours$215k - $264k
...leading the fight against MASH.Madrigal’s medication, Rezdiffra (resmetirom), is a once-... ...the right time, in the right way.The Director, Clinical Scientist, will support the development and... ...leadership 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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...to conduct and/or monitor toxicity studies (GLP and non-GLP) as a Study Director or Study Monitor. Toxicologists... ...the findings from all contributing scientists into reports that characterize the... ...benefits. Available benefits include medical, dental, vision healthcare and...SuggestedFull timeFor contractorsLocal area$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,...SuggestedMinimum 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- ...recognize their merit.Job Function: Medical Affairs GroupJob Sub Function: Medical... ...Affairs organization as an Associate Director, Clinical Scientist, Gastroenterology located in Horsham,... ...support the conduct/execution of clinical studies, advancement of collaborative &...Full timeWork experience placementWork at officeLocal areaRemote work2 days per week
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- ...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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...Program Implementation Manager, Clinical Studies. This position can be home-based.... ...facilitation of educational opportunities, intervention tracking, and process mapping. This person... ...offer a wide array of benefits including medical, dental, vision, disability, and life...Full timeWork at officeLocal areaRemote workWork from homeNight shift$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 ManagerAt Real we're always looking for new and ambitious people to help deliver exceptional service levels, change the... ...with some of the world's best pharmaceutical, biotechnology and medical companies.As specialists in recognising talent we pride ourselves...Local areaFlexible hours
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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$194k - $334.65k
...people living with immune diseases. The Medical Director provides medical and scientific... ...development. The role leads assigned studies and contributes to program strategy, with... ...leading or materially contributing to interventional clinical trials, including protocol development...Full timeLocal areaImmediate start$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 startWork from home- A leading clinical research organization is seeking a Clinical Study Manager to oversee clinical studies. Responsibilities include supporting site management, ensuring compliance with regulations, and solving complex project issues. The ideal candidate will have 5+ years...Remote job
- ...evaluates and treats patients in an applicable medical and/or surgical specialty or... ...others, as needed.Performs therapeutic interventions to stabilize acute and critical health problems... ...provide feedback and consultation for studies as they progress.Delegate operational functions...Full timePart timeTraineeshipWork at officeLocal area
$70k - $78.3k
...B. Braun Medical Inc., a leader in infusion therapy and pain management... ...S., which includes B. Braun Interventional Systems, Aesculap® and CAPS®... ...and support drug stability studies, including protocol... ...guidance and support to junior scientists and laboratory personnel....- A healthcare provider is seeking a professional to assist the Invasive Cardiologist with diagnostic and interventional procedures, ensuring efficient department functioning. The ideal candidate must have 3 years of relevant experience and certifications in cardiac radiography...
- A healthcare provider in Clairton is seeking an experienced professional to assist Invasive Cardiologists in diagnostic and interventional procedures. The ideal candidate will have a minimum of 3 years' experience in a cardiac cath lab, relevant certifications, and strong...
- ...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
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- ...Opportunity FirstEnergy Corp is looking to fill one (2) mid-level scientist positions in Greensburg or Reading, PA, Holmdel, NJ, Morris... ..., Botany, Wildlife/Zoology, Environmental or Physical Sciences/Studies, Engineering or related field from an accredited college/university...Local areaNight shift
- ...Our Opportunity We are currently seeking a Human Factors Scientist for our Human Factors Practice in Philadelphia, PA for a Summer... ...range of consulting activities that involve usability testing, study and survey design, human factors in accidents and their prevention...Full timeSummer workWork at officeRelocationFlexible hours
- In vitro ADME Senior/Principal Scientist - DMPKLocation: Exton, PA Department: DMPK (Drug Metabolism & Pharmacokinetics)Employment Type:... ...interpretation, and reporting of a broad range of in vitro ADME studies supporting drug discovery and IND-enabling programs.Roles &...Contract workTemporary work
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