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$147.3k - $220.9k
Position Summary:The Associate Director, Study Management will work effectively across multiple scientific teams to direct the delivery of study... ...work to support analysis of assays for non-regulated, GLP-regulated, GCP-regulated and commercial diagnostic (CLSI, CLIA...SuggestedLocal areaPrecision Medicine Group
Frederick, MD3 days ago- ...join our team in Madison, WI!Job Responsibilities:The Senior Study Director will have extensive Met-ID experience and is responsible for managing... .... Applies up to date knowledge and application of current GLP, GCP, GMP and regulatory guidelines relevant to study conduct....SuggestedTemporary workCasual workInternshipRelocation packageFlexible hours
Laboratory Corporation of America
Madison, WI1 day ago $147.3k - $220.9k
The Associate Director, Study Management will work effectively across multiple scientific teams to direct the delivery of study milestones within... ...work to support analysis of assays for non-regulated, GLP-regulated, GCP-regulated and commercial diagnostic (CLSI, CLIA...SuggestedLocal area$95k - $130k
Study DirectorTitle: Study Director; Developmental and Reproductive Toxicology (DART)Location: Chicago, IL (on-site)Reporting to: VP of ToxicologyFull... ...communication skills required.Thorough understanding of GLP regulatory requirements, and various toxicology testing guidelines...SuggestedContract workTemporary workImmediate startFrontage Laboratories
Chicago, IL14 hours ago- ...CDMO, advanced material sciences and in the support of clinical studies.Job DescriptionSupervise and assist in the conduct of regulatory... ...development, design and implementation.Responsibilities as stated in GLP regulations.Data interpretation and report writing.Client...SuggestedFull timeMonday to Friday
Eurofins
Trenton, NJ14 hours ago $171.2k - $256.8k
...Avenue, in the Fenway area of Boston, Massachusetts.SummaryThe Director, GCP & GLP QA, reporting to the Executive Director, Quality, is... ...readiness, and vendor oversightProvide QA oversight of GLP studies at contract research laboratories, including facility/study...SuggestedContract workTango Therapeutics
Boston, MA2 days ago- Director of Study Management# Director of Study ManagementHot JobMillcreek , UT 84106## OverviewPosition TypeFull Time## DescriptionPrimary Purpose... ...), Study Director, or equivalent leadership role supporting GLP and/or GCP bioanalytical studies.* Minimum 5 years of people...SuggestedContract workWork at office
- Precision Medicine Group seeks an Associate Director, Study Management to lead study delivery across Bioanalytical, Companion Diagnostic, Flow... ...management experience, with strong leadership and regulatory experience (GLP/GCP). #J-18808-Ljbffr Precision Medicine GroupSuggested
- ...Medicine Group, LLC. in Frederick, Maryland, seeks an Associate Director, Study Management to direct delivery of study milestones across... ...scientific teams, manage budgets, and ensure quality and compliance in GLP/GCP-regulated studies. You will lead a team of Project...Suggested
- ...This is a remote role. Oncology experience is required for this role and cell therapy is strongly preferred! The Local Study Associate Director (LSAD) leads Local Study Team(s) (LSTs) at country level to deliver committed components of clinical studies according to...SuggestedLocal areaRemote workFlexible hours
PAREXEL
Ewing, NJ1 day ago - ...The Associate Clinical Study Manager (ACSM) supports the planning, execution, and oversight of clinical trials to ensure studies are conducted in compliance with study protocols, company SOPs, and regulatory requirements. This role works closely with cross-functional...SuggestedFull timeContract work
Advanced Recruiting Partners
United States3 days ago - ...company, is seeking a Microbiologist II to join our New Jersey team to conduct a variety of microbiology analyses and ensure studies comply with GMP/GLP/ISO and client specifications. The candidate will train staff and participate in SOP approvals. Responsibilities include...Suggested
$160.8k - $201k
...benefits, see our website: The Importance of the Role We are seeking an associate director-level candidate with clinical operations experience, with specific expertise in feasibility and study start-up, who is interested in applying their experience to develop, build out,...SuggestedFull timeSarepta Therapeutics
Somerville, MA1 day ago$142.4k - $224.1k
Job DescriptionRole Overview:The Associate Director, Study Data Services leads and develops a programming and reporting team - set goals, assign work, coach performance, and manage recruiting/onboarding - while communicating status and risks to leadership and partners....SuggestedFull timeFor contractorsLocal areaVisa sponsorshipFlexible hoursMerck Sharp & Dohme (MSD)
Rahway, NJ3 days ago- MSD is seeking an Associate Director, Bioanalytical Laboratory in Gaithersburg, MD. You will lead the bioanalytical lab, directing assay validations and sample testing while ensuring GLP/GCLP compliance and staff proficiency. You will collaborate with senior management...Suggested
- The University of Texas at Austin invites applications for Associate Director of the Texas Center for Disability Studies (TCDS) to lead UCEDD and LEND programs. This senior role reports to the Executive Director and works with faculty, staff, partners and people with disabilities...
$137.94k - $206.91k
Job Title: LSAD (Local Study Associate Director) Location: Field At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are...Hourly payTemporary workLocal areaWorldwideFlexible hours$75k - $115k
Job Posting Title: Associate Director - Texas Center for Disability Studies Hiring Department: School of Social Work Position Open To: All Applicants Weekly Scheduled Hours: 40 FLSA Status: Exempt from FLSA Earliest Start Date: Jan 11, 2027 Position Duration: Expected...Full timeFor contractorsWork at officeLocal areaFlexible hoursShift work- ...Summary Take the next step in your fundraising career by joining us as the Associate Director of Alumni Relations and Annual Giving at UCLA’s School of Education and Information Studies (Ed&IS). In this multi-faceted role, you will be an essential driver of alumni and...Weekend workAfternoon shift
$109.9k - $179.3k
...Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Clinical Study Associate Manager to join our Clinical Trial management team. In this role, you will support the Clinical Study Lead by taking...Full timeContract workWorldwideRegeneron Pharmaceuticals
Tarrytown, NY3 days ago- ...AbbVie, please visit us at Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube. Job Description The Senior Director, Global Study Start-Up (SSU) is accountable for leading study start-up strategy, talent, and execution across the AbbVie portfolio. This...Local area
$165k - $200k
...individuals, families and communities. Learn more at , and follow us on X, LinkedIn and Facebook.Role Summary:The Clinical Operations Study Lead ensures that clinical strategies are translated into operational plans and executed in line with clinical development plans (...Local areaDyne Therapeutics
Waltham, MA2 days ago$90k - $130k
Job Title: Associate Director, Inlife Operations Location: Chicago, IL Reports to: Vice President... ..., dermal, ocular, and carcinogenicity studies in support of pharmaceutical and... ...accordance with approved study protocols, SOPs, GLP requirements, and applicable regulatory...Contract workTemporary workImmediate startFrontage Laboratories
Chicago, IL3 days ago$185.85k - $251.44k
...them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Director, Study Evidence & Readiness What you will do Let’s do this. Let’s change the world. In this vital role you will lead the Study Evidence...Full timeWork experience placementFlexible hours$19.95 - $39.66 per hour
...workplace where people thrive by being themselves and are inspired to do their best work every day.Join us! What the Associate Clinical Study Manager does at Worldwide The Associate, Clinical Study Manager will be responsible for the site-level monitoring activities of on...Hourly payLocal areaWorldwide$80.1k - $105.5k
...guidelines Adherence to federal and/or local regulations as applicable Essential Position Responsibilities: Serve as the Study Director for non-GLP and GLP studies and performs the following duties for assigned studies: Prepare study protocols/amendments and assure that...Temporary workLocal area$98.1k - $160.1k
...with limited supervision to support the Toxicology department. You will contribute to toxicology studies and/or program development through study monitoring of outsourced non-GLP and GLP studies through remote and onsite CRO monitoring and other activities as assigned by...Full timeRemote work- Job Title: Associate Director, Clinical Development & OperationsLocation: Columbus, OHJob Type... ...for multiple complex bioequivalence studies. Managing internal and external resources... ...knowledge and thorough understanding of GMP, GLP, GCP and FDA requirements for drug...Full timeFor contractorsWorldwide
Hikma Group
Columbus, OH14 hours ago $298.7k
...authorization. External applicants must be eligible to work in the US. We are seeking an experienced clinical development leader to head the Study Start-Up Unit and provide strategic direction, operational oversight, and expert leadership across study start-up activities for the...Contract workFlexible hoursMerck
Billerica, MA3 days ago- ...once-monthly dosing, as well as MBX 6180, a GLP/GIP/GCGR triple agonist prodrug for once... ...Summary MBX is seeking an Associate Director, Statistical Programming to lead and contribute... ...for planned analyses, including study monitoring, data reviews, clinical study...For contractorsWork at officeLocal area
MBX Biosciences
Burlington, MA5 days ago
