Interventional Study Scientist Medical Director
Scorpion Therapeutics
Reports to: Head of Interventional & Supported Studies In this role, you will: 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. Prepare and present study results for scientific meetings, publications, and regulatory submissions. Engage internal/external stakeholders (e.g., investigators and thought leaders) to enhance study design and execution. Basic Qualifications & Skills (required): Advanced degree in a relevant scientific discipline (MD, PhD, PharmD, or equivalent). Substantial experience leading interventional clinical studies in therapeutic areas such as oncology/haematology/immunology/specialty. 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. Excellent communication and organizational skills. Preferred Qualifications & Skills: Experience leading global Phase IIIb/IV interventional studies. Experience collaborating with regulatory authorities. Familiarity with innovative clinical trial design/execution approaches. Experience developing scientific content for publications and regulatory submissions. Understanding of digital tools/methodologies for evidence generation. Experience leading cross-functional teams in a matrixed environment. #J-18808-Ljbffr Scorpion Therapeutics
- Scorpion Therapeutics is seeking a senior professional to lead interventional clinical studies and oversee governance, safety data review, and risk mitigation. You will guide protocols, analysis plans, and interpretation of results while ensuring patient safety and scientific...Suggested
- ...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...SuggestedLocal areaImmediate startRemote work
$176.6k - $294.3k
The Clinical Development Scientist (Director) is responsible for scientific oversight, data integrity... ...clinical deliverables for one or more studies. They may also manage, supervise, and... ...Team meetings in collaboration with Medically Qualified Individual(s); reviews...SuggestedPermanent employmentFull timeH1bLocal areaVisa sponsorshipWork visaRelocation package2 days per week$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$96.2k - $151.4k
...and Development division, quantitative scientists, in partnership with other subject matter... ...approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of... ...clinical schedules in support of clinical study randomization and data unblinding under...SuggestedFull timeFor contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work- 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
$142.4k - $224.1k
...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...Full 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,...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- The Senior Medical Director, Oncology Clinical Development - GU will report... ...with physicians, scientists, regulatory professionals,... ...develop and execute phase 1-3 interventional clinical trials. Represent... ...protocol concept to final study report ensuring scientific...Local areaWorldwide
$274.5k
...Purpose This position is for a Senior Medical Director within the Hematology program. This individual... ...: Clinical Development Leadership on Study Teams and Development Subteams Serves... ..., in collaboration with Clinical Scientist and the cross-functional team. Strategic...Permanent employmentFull timeH1bLocal areaVisa sponsorshipWork visaRelocation package2 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$239.9k - $399.8k
...position is for a Clinical Development Medical Director within the prifetrastat program. This individual... ...Development Leadership on Study Teams and Development SubteamsConduct medical... ..., in collaboration with Clinical Scientist and the cross-functional team.Provide clinical...Permanent employmentFull timeInternshipH1bLocal areaVisa sponsorshipWork visaRelocation package2 days per week- ...Collegeville, PA. Discover Impactful Work The Senior Research Scientist independently performs, oversees, and directs a variety of... ...develop analytical methods and/or other specialty technologies studies that meet client requirements. • Acts as on-site Subject...Full timeContract workWork at office
- ...Conditions Office Job Description Job Description Role: Scientist, Biomarkers This is a fully onsite role based at our... ...responsibilities, ensuring data quality, accuracy, and adherence to study timelines. Document all laboratory activities clearly and...Full timeWork at officeRelocationRelocation package
- ...Clinical Scientist A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri... ...Responsibilities: • The supporting clinician will provide medical and scientific study and project support for multiple, global, Phase 1-4...
- ...seeks an experienced health outcomes/real-world evidence scientist to develop and execute studies supporting launch optimization and payer evidence across liver disease therapies. You will collaborate with medical, market access, R&D and commercial teams, design robust...
- ...approach to R&DPosition SummaryAre you a scientist in sterile drug product development... ...techniques and development (non-GMP) stability studies to optimize protein formulation. The... ...LISkillsDrug Delivery, External Manufacturing, Medical Device Evaluation, Molecular Modeling,...Local area
- GlaxoSmithKline seeks a scientist to lead protein formulation and drug product development within the DPD/FPD team. Focused on biopharmaceutical... ...assets, you will drive formulation optimization, stability studies, and process development for protein therapeutics (mAbs, ADCs,...
- ...injectables, mAbs and oligonucleotides. You will design and run studies, interpret results, and make clear recommendations. You will... ...team environments. Skills Drug Delivery, External Manufacturing, Medical Device Evaluation, Molecular Modeling, Pharmaceutical...Local areaRemote work
- A Medical Affairs Medical Director has strong clinical and scientific training and can take on many aspects of medical affairs work (insight generation... ...work. Provides input into the design of Phase IIIB/IV studies and real-world evidence studies (RWE) to address key...Local area
- GlaxoSmithKline is seeking a Medical Affairs Medical Director to provide clinical and scientific input across the medicine strategy, develop tactical... ...care. The candidate will contribute to Phase IIIB/IV study design, real-world evidence, and medical communications,...
$295.9k
...position is for a Clinical Development Medical Executive Director supporting Thoracic Cancers. The... ...and external stakeholder input into study designs Serves as primary interface with... ...documents, in collaboration with Clinical Scientist and the cross-functional team Oversee...Permanent employmentFull timeH1bLocal areaVisa sponsorshipWork visaRelocation package2 days per week- GSK seeks a scientist to lead formulation and process development for sterile and complex drug products, including long-acting injectables. You will design studies, interpret data, and collaborate with regulatory and supply teams to progress development and transfer to...
$203.78k - $339.63k
...and patients. Responsibilities Plan, design and execute multiple studies for a given asset and manage timelines, deliverables, and... ...to the decision making of different customers (reimbursement, medical societies, physicians). Collaborate with internal teams and participate...Local areaFlexible hours$284.63k
Senior Medical Director, Clinical Development, Neurodegeneration GSK is seeking a highly skilled Senior Medical Director, Clinical Development... ...probability of technical success PTRS evaluations and assess study/project risk-benefit, implementing mitigation strategies as...Work at officeLocal area2 days per week$156.9k - $247k
...person will lead several Human Factors scientists to perform and manage human factors activities... ...for all combination products and medical devices in our company's portfolio and pipeline... ...for use, conducting formative/summative studies, preparing regulatory submission...Full timeFor contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work$231.9k - $365k
...to join a highly collaborative team of scientists (12 anatomic pathologists, 3 clinical pathologists... ...in a wide variety of GLP-toxicology study types, many of which are run in-house,... ..., In Vivo Models, Laboratory Processes, Medical Biology, Molecular Diagnostic Techniques...Full timeFor contractorsLocal area- ...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
$87.3k - $137.4k
...seeking a highly motivated and skilled Scientist to join our collaborative, dynamic, and... ...integral role in executing in vivo research studies in both rodents and non-rodents and... ...care.• Clinical Care: Carry out prescribed medical treatment and research regimens for study...Full timeFor contractorsLocal areaImmediate startRotating shift
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