Clinical Study Manager
Relay Therapeutics
Relay Therapeutics in Cambridge, MA is seeking a Manager, Clinical Science to drive asset development and implement the clinical strategy. You will collaborate with clinical PM, regulatory affairs, operations, biostatistics, data management and medical writing to advance studies and provide strategic scientific input. You will design studies, direct protocol development, oversee DSUR timelines, and support regulatory questions while ensuring data quality and integrity across initiatives with #J-18808-Ljbffr
$95k - $105k
...on a range of projects involving the set-up and management of de novo, global real-world evidence (RWE) studies, including ethics applications and site support Salary... ...About the Role We are seeking an experienced clinical research professional to join the RWE team at Costello...SuggestedPermanent employmentFull timeContract workTemporary workWork at officeLocal areaWork from homeFlexible hours- ...Clinical Study Manager Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission...SuggestedContract work
- ...services company powering the acceleration of clinical research to transform patient outcomes.... ...world-wide. The Research Finance Manager is a senior leader at the intersection of... ...leadership, and the operational rigor to keep study startup moving efficiently at scale. Where...SuggestedContract workTemporary workFor contractorsFor subcontractorH1bWork at officeLocal areaWork visa2 days per week
$137.8k - $206.8k
...Job DescriptionGeneral Summary:The Senior Manager, Clinical Study Quality Lead provides study-level quality oversight for assigned clinical trials to help ensure they are conducted in compliance with Good Clinical Practice (GCP), applicable global regulations, study protocols...SuggestedSummer workRemote workFlexible hours2 days per week$164k - $199k
...scientific or healthcare discipline, with 8+ years of clinical operations experience, including 4+ years as a clinical trial manager, leading cross-functional teams and... ...management activities and lead the cross-functional study teamContribute to the development and...SuggestedContract workLocal area- POSITION OVERVIEWScience 37 accelerates clinical research by expanding patient access to trials, leading to faster approvals and... ...traditional means of conducting clinical research.The Clinical Study Design Manager is responsible for working with our clients and internal...Work at officeFlexible hours
$145k - $175k
...Vascular Laboratory Manager When you join the growing BILH team, you're not just taking... ...lives. Oversee the programmatic and clinical operations management of the Vascular... ...compliment of staff to perform vascular studies and procedures. Develops and maintains...Work experience placementInterim roleWork at officeShift work- ...Senior Clinical Data ManagerOdyssey Therapeutics is propelling drug development beyond what is now possible... ...opportunity:Odyssey is seeking a Senior Clinical Data Manager to own clinical data management deliverables from study start-up through close-out. Reporting to the...
- ...BeOne Medicines USA, Inc. in Cambridge, MA seeks a Manager, EDC Administration to lead Data Management administration for US-based clinical studies, coordinating with CTMS, IRT, and MDW integrations, and supervising EDC Admins. This is a full-time role with a telecommuting...Full timeRemote work
- ...Clinical Data Manager A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well... ...capabilities to achieve quality, timely, cost-effective study deliverables. • Coordinating program work of Data Manager...Work at office
- ...Clinical Data Management Leader Provide leadership, strategic planning, direction and implementation of clinical systems for data collection... ...budgeting, resource planning, vendor oversight, EDC build and study timelines, etc. Perform or provide oversight to staff...
- ...liaison between Company and CRO for Data Management. Provide support and oversight for... ...Management team. Collaborate with the team on study design, protocol development, CRF design... ...planning, and CSRs. Review clinical study protocols and provide comments if...
- ...Moderna Services, Inc. is seeking a Sr. Manager, Clinical Data Management to lead data management activities and vendor oversight for clinical studies in Cambridge, Massachusetts. You will ensure milestones are met with quality and represent your function in cross-functional...Remote work
$119k - $179k
...Clinical Operations Manager The Clinical Operations Manager serves as a dedicated functional expert within a cross-functional team, contributing... ...expertise to ensure operational execution of clinical studies. This role focuses directly on driving core operational milestones...Full time- ...Manager, Clinical Marketing Our organization is a rapidly growing Boston-based life science company whose mission is to save lives of patients... ...initiatives and tools, which may include development of case study series, competitive toolkits (customer facing and internal...Work at officeLocal area
- Biogen is seeking a Data Manager in the Implantable Device Unit to lead clinical data management for studies, coordinating with internal teams and external CROs. You will develop data management plans, ensure protocol alignment, and generate data listings and summaries...
$237.2k - $372.79k
...to shine? Join us as a Medical Director, Clinical Science, GI2 TAU in our Cambridge, MA... ...and other documents needed for CDP and study execution and regulatory submissions. Recommends... .... Presents study conclusions to Management and determines how individual study results...Minimum wageFull timeTemporary workWork at officeLocal areaRemote workNight shift$177k - $278.08k
...Position Objectives: Drives, or contributes to, strategy for clinical studies within the overall global clinical development for assigned... ...significance to individual patients.May present study conclusions to Management and determine how individual study results impact the...Minimum wageTemporary workLocal areaNight shift- ...to join the team as our Senior Director, Clinical Sciences. This is a hands-on leadership... ...analysis, and interpretation of clinical studies. You will ensure scientific rigor... ...oncologyDemonstrated experience in designing and managing clinical trials, including knowledge of...
$220k - $245k
...understanding of their bodies and daily lives.As the Director, Clinical Science, you will lead the clinical science function responsible... ...deep expertise in SaMD clinical development, including study design, endpoint development, clinical validation, regulatory strategy...Full timeWork at officeRemote workRelocation- ...engagement for multiple early-stage CNS clinical programs, including assets being developed... ...meaningfully impact clinical development plans, study design, and data interpretation.Lead and... ...’s early asset portfolio.Organize and manage global expert events (advisory boards,...Full timeTemporary workLocal areaFlexible hours
$120.2k - $180.4k
...DescriptionGeneral Summary:The Medical Writing Science Manager is responsible for preparing moderately complex clinical and regulatory documents and represents Medical... ...as a cross-functional team member at clinical study level activities. This role contributes...Full timeSummer workRemote workFlexible hours2 days per week- Job DescriptionGeneral Summary:The Clinical Pharmacology Director leads strategic, scientific... ...plans; assists in departmental management through program reviews and collaborative... ...PharmacologyExperience conducting and supervising clinical studies such as drug-drug interaction, special...Full timeSummer workRemote workFlexible hours2 days per week
$225k - $315k
Cambridge, MADevelopment - Clinical Pharmacology /Full-Time /On-siteScholar Rock is a late-stage global biopharmaceutical company focused... ...Development (MIDD).Contribute to clinical protocol design, study execution, data analysis, and writing clinical study reportsCollaborate...Full time$206.25k - $343.75k
...serves as a valued strategic partner with Clinical, Commercial, Regulatory, and Market... ...with field teams, global teams, alliance management and the relevant U.S. cross-functional partners... ...execution of US Phase IIIB-IV clinical study programs, including preparation of study...Full timeLocal area$257.6k - $404.8k
.... Join us as a Senior Medical Director, Clinical Science Neuroscience, in our Cambridge,... ...leadershipLeads Global (US/EU/Japan) Development Team managing both the US/EU Development Team and the... ...data from ongoing internal and external studies, assessing the medical and scientific...Minimum wageTemporary workWork at officeLocal areaRemote workNight shift$206.25k - $297.92k
...serves as a valued strategic partner with Clinical, Commercial, Regulatory, and Market... ...Medical Directors, Medical Science Liaison Managers, and Medical Science Liaisons) by cultivating... ...execution of US Phase IIIB-IV clinical study programs.Support the review and approval...Full time- ...DescriptionGeneral Summary:The Senior Director, Clinical Pharmacology will serve as a Disease Area... ..., Clinical Pharmacology will also manage the scientific functions and coordinate the... ...execute Clinical Pharmacology plans and studies for Disease Area programsDirects Clinical...Full timeSummer workRemote workFlexible hours2 days per week
$200k - $250k
....The RoleWe're looking for a Director of Clinical Affairs who will own the end-to-end execution of our regulatory-driven clinical studies. This is a hands-on, operationally intense... ...how to stand up a study from scratch, manage third-party clinical sites, write IRB and...Full timeContract workImmediate startWorldwideNight shift$183.8k - $330.3k
...Therapeutic programs, specifically supporting the Clinical Development Lead in the direction,... ...and evaluation of Phase 1-3 clinical studies. The principal responsibility for this... ...Clinical Safety & Pharmacovigilance, support managing study sites to ensure that study...Permanent employmentFull timeWork at officeWork from home
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