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- ...seeking a Microbiologist III in Lincolnshire, IL. This role conducts a variety of test methods and serves as study director, ensuring tests comply with GMP/GLP/ISO and client specifications. You will train incoming staff and help approve SOPs and protocols. Responsibilities...Suggested
$160k - $240k
...tenacity to overcome barriers, together.Opportunity OverviewAs the Associate Director, GCP/GLP/GVP QA, you will oversee GCP activities, ensure compliance and quality execution of clinical studies. You will assist in the development and management of GCP quality processes...SuggestedContract workWork at officeImmediate startNight shift$140k - $160k
Frontage Laboratories, Inc. is seeking an Associate Director/Director of Toxicology in Chicago, IL. This full-time role focuses on leading Developmental and Reproductive Toxicology studies, managing scientific teams, and ensuring regulatory compliance. Ideal candidates...SuggestedFull time- ...University of Texas Medical Branch is seeking a Regulatory Scientist II in Galveston, TX. This role focuses on managing scientific studies compliant with U.S. FDA regulations while overseeing project design and execution. The ideal candidate will have extensive experience...Suggested
- ...’re improving health and improving lives.Labcorp is seeking a Study Director - DART, Chemical and Crop Protection to join our dynamic team... ...are conducted in full compliance with Good Laboratory Practice (GLP) requirements to support global regulatory submissions.Plan,...SuggestedTemporary workCasual workInternshipRelocation packageFlexible hours
- ...’re improving health and improving lives.Labcorp is seeking a Study Director I - Metabolism to join our team in Greenfield, IN!Job Responsibilities... ...Job Standards:Awareness of requirements for working within a GLP, GCP and GMP (as appropriate) environment Basic awareness of...SuggestedTemporary workCasual workInternshipRelocation packageFlexible hours
$80.1k - $105.5k
Inotiv is looking for a Study Director in Rockville, Maryland, who will oversee study designs, manage regulatory compliance, and interact with sponsors. Qualified candidates should have a Ph.D. or a Master's degree in a scientific discipline, with relevant experience in...Suggested$172.6k - $233.4k
The Associate Director Study Management (AD Clinical Operations) is responsible for leading a team of Global Trial Leaders and Trial Managers within the Study Management Organization. The position is responsible for staff development and study oversight, and will work...SuggestedFull timeTemporary workLocal areaRemote workFlexible hours- ...CDMO, advanced material sciences and in the support of clinical studies. Job Description Supervise and assist in the conduct... ...development, design and implementation. Responsibilities as stated in GLP regulations. Data interpretation and report writing....SuggestedFull timeMonday to Friday
Eurofins USA BioPharma Services
South Brunswick, NJ16 days ago - ...Job Description Job Description Study Director – Non-Human Primate Research Program Location: Corpus Christi, Texas Job Type:... ...with an emphasis on sponsor-facing roles. ~ Familiarity with GLP/GCP environments is an asset, however, at this time the facility...SuggestedFull timeWeekend work
RPM ReSearch
Corpus Christi, TX27 days ago - ...The Local Study Associate Director (LSAD) leads Local Study Team(s) (LSTs) at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying with Client Procedural Documents, international guidelines such...SuggestedLocal areaFlexible hours
PAREXEL
Honolulu, HI1 day ago $137.94k - $206.91k
...Are you ready to lead country execution of pivotal clinical studies and help bring new cancer medicines to patients faster? This is your... ...and advances the standard of care! As a Local Study Associate Director, you will lead cross-functional Local Study Teams to deliver...SuggestedWork at officeLocal areaFlexible hours3 days per weekAstraZeneca
Wilmington, DE4 days ago- Associate Director, University Studies, Transition Programs Department: Academic Affairs Classification: Professional Faculty Job Category: Administrative or Professional Faculty Job Type: Full-Time Work Schedule: Full-time (1.0 FTE, 40 hrs/wk) Location: Fairfax,...SuggestedFull timeWork at office
$143.3k - $193.3k
...motivated, collaborative, and most importantly, share our passionate interest in fighting cancer. ~Provides management to Global Study Management Associates (gSMAs) at various levels in one or multiple regions, including line management, mentorship, coaching, and personal...SuggestedFull timeLocal areaBeiGene
Remote5 days ago- Charles River Laboratories in Horsham, PA is seeking an experienced Study Director to oversee preclinical efficacy and toxicology studies. You will design study plans, schedules, ensure GLP compliance, and coordinate protocols with technical teams. You will prepare reports...Suggested
$81.6k - $111.53k
...Job Description Working under the supervision of the Associate Dean for Undergraduate Studies, the Associate Director of Undergraduate Studies in the Schaefer School of Engineering and Science (SES) is responsible for the day-to-day operations of the Undergraduate Studies...Part timeFor contractorsWork at officeStevens Institute of Technology
Hoboken, NJa month ago$178k - $218k
...strategy to ensure we have the right talent, at the right time, in the right way.Madrigal Pharmaceuticals is seeking an Associate Director, Study Toxicologist to support nonclinical development programs for metabolic dysfunction-associated steatohepatitis (MASH). This role...Minimum wageFull timeContract workLocal areaFlexible hours- ## Associate Director, Talent Management, School of Professional StudiesApplylocations: Pearl Education Buildingtime type: Full timeposted... ...role in a school on the move? The School of Professional Studies (SPS) is in a period of exciting, rapid growth, and we are looking...Full timeWork at officeWeekend workAfternoon shift
- Introduction to roleAre you ready to lead the charge in groundbreaking clinical studies? As a Global Study Director (GSD), you will play a pivotal role in the Cell Therapy Clinical Operations organization, driving the operational planning and delivery of high-priority and...Full time
- ...journey, HLS is a place where you can thrive, contribute, and be part of something bigger.Job DescriptionThe Senior Director of International Legal Studies is a key member of the leadership team for the Graduate Program and International Legal Studies with primary...Remote work
- ...that serve as a vital resource for advanced research in global studies for the consortium, the CUNY system, and scholars worldwide. NYPL... ...and diversity of their international holdings. The Associate Director will also work with stakeholders across the Library and with...Worldwide
$195k - $275k
...inclusivity, so that our people are valued, seen, and heard.How you’ll contribute:Provide strategic and operational leadership for end‑to‑end study start‑up activities across assigned clinical programs, ensuring timely, compliant, and high‑quality site activation.Accountable for...Contract workLocal area$194.12k - $242.65k
...Director, GLP-1 and Cardiometabolic Health Program Manager Remote, USA Omada Health is on a mission to bend the curve of chronic disease. Job overview Omada Health is seeking a Director to drive the day-to-day execution and operations of our GLP-1 solutions within...Local areaRemote workWork from homeFlexible hoursOmada Health
United States4 days ago$143.3k - $193.3k
General Description Provides management to Global Study Management Associates (gSMAs) at various levels in one or multiple regions, including line management, mentorship, coaching, and personal/career development. Responsible for assignment of qualified gSMA resources to...Hourly payLocal areaWorldwide$185.68k - $242.65k
Role Description Omada Health is seeking a Director to drive the day-to-day execution and operations of our GLP-1 solutions within our broader cardiometabolic platform. This leader will help translate Omada’s GLP-1 strategy into clear plans, workflows, and cross-functional...Full timeRemote workWork from homeFlexible hoursOmada Health
Remote3 days ago- NIS P&D Study Delivery Lead, Associate Director - Oncology For candidates seeking to be located at our Stevenage site, this role will temporarily be based at Stevenage. However, the Company plans to relocate its offices to Cambridge, UK. The location of this role will therefore...Full timeWork at officeLocal areaRemote workRelocation
$19.95 - $39.66 per hour
## Associate Clinical Study Manager (San Antonio, Tx)Applyremote type: Hybridlocations: San Antonio, Texastime type: Full timeposted on: Posted Todayjob requisition id: JR102659Who we areWe’re a global, midsize CRO that pushes boundaries, innovates and invents because the...Hourly payLocal areaWorldwide- Participant Recruitment & Study Startup Manager About ClariMed, Inc. ClariMed is a human-centered development and regulatory practice for medical products developed by Pharmaceutical and Medical device manufacturers. Our best-of-breed professional services cultivate innovation...
$120k - $160k
...more accessible for all. To learn more about Care Access, visit How This Role Makes a Difference Reporting to the Sr. Director of Study Feasibility & Clinical Partnerships, the Associate Director and Director of Study Feasibility & Clinical Partnerships provides...Full timeTemporary workWork at officeLocal areaRemote workWorldwideVisa sponsorshipWork visaFlexible hoursCare Access
Boston, MA23 days ago$165k - $185k
...resonates, read on.About the Role: The Associate Director, Biomarker and Assay Development will... ...interpret translational and preclinical studies, including studies evaluating editing... ...assaysExperience supporting IND-enabling studies, GLP toxicology studies, and regulatory...Work at office
