Clinical Study Manager
Aimwel
Provide operational leadership, coordination, and oversight for assigned clinical studies. Ensure studies are conducted in compliance with ICH/GCP guidelines, regulatory requirements, company SOPs, study protocols, and study-specific plans. Partner with cross-functional teams, CROs, vendors, investigators, and study sites to deliver high-quality studies on time and within scope.
Vacancy posted 1 day ago
Similar jobs that could be interesting for youBased on the Clinical Study Manager in Durham, NC vacancy
$56.99 - $71.32 per hour
...Job Title: Clinical Study Manager Pay Rate: $56.99 - $71.32/hr. Location: Durham, NC ZIP Code: 27701 Start Date: Right Away Shift: 8:00 AM- 5:00 PM Keywords: #ClinicalStudyManagerjobs #Durhamjobs Job Description The Contract Clinical Study Manager provides operational...SuggestedContract workWork at officeLocal areaImmediate startShift work- Intellectt Inc is seeking a Contract Clinical Study Manager in Durham, NC to provide operational leadership for assigned clinical studies. You will coordinate with CROs, vendors, investigators, and site personnel to deliver milestones on time and within quality standards...SuggestedContract work
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$85 - $95 per hour
Position Overview We are seeking a Clinical Operations Manager for a global Phase II pan‑tumor oncology trial. This is a 100% remote role, preferred... .... Responsibilities Own operational accountability for study‑level time, cost, and quality deliverables for a global Phase...Hourly payContract workTemporary workRemote work$93.1k - $232.8k
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...Job Description Job Description Title: Clinical Study Manager Hiring Organization: Connexion Systems & Engineering Compensation, Benefits, and Employment Type Duration: 1+ year contract, possible extension Pay rate: $56.99–$71.32/hour Job Location:...Contract workWork at officeMonday to Friday- Belcan Corporation in Durham, NC is seeking a Contract Clinical Study Manager to provide operational leadership and oversight for assigned studies, ensuring adherence to ICH/GCP, regulatory requirements, SOPs, and study plans across CROs, vendors, investigators, and sites...Contract work
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$110k - $145k
About the Role The Principal Clinical Data Manager (PCDM) is primarily responsible for providing in-depth guidance as Subject Matter Expert in... ...outside of Biometrics. Responsibilities 1. Projects/Clinical Studies Participate in project meetings and client meetings as...Flexible hours$80k - $106k
The Supervisor, Clinical Laboratory oversees day‑to‑day operations of assigned laboratory areas... ...established performance specifications. Manage scheduling, staffing, and workload... ...and operations within a regulated clinical study environment (ICH E6 (GCP), ISO 20916, FDA...Full timeWork at officeLocal areaFlexible hoursShift workNight shiftAfternoon shift- ...which transplant is not currently an option. Who You Are The Clinical Supply Chain Manager, Strategic Development will manage the manufacture, supply... ...packaging and labeling Attend and participate in study‑related meetings to build cross‑functional relationships,...Contract workTemporary workWork experience placement3 days per week
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...Essential Functions Manage staff in accordance with organization’s policies and applicable regulations.... ...applicable. Participate in the allocation of resources to clinical research projects by assigning staff to clinical studies based on their experience and training. Manage...Full timePart timeImmediate start$57 - $71 per hour
...operational leadership, coordination, and oversight for assigned clinical studies. Ensure studies are conducted in compliance with ICH/GCP... ...on time and within scope. Primary Responsibilities Manage day-to-day clinical study activities from study start-up through...For contractorsWork at office- Executive Director, Oncology Clinical Pharmacology Modeling and Simulation We have an exciting... .... provide managerial support to CPMS Managers and Directors. Individuals will be... ...initial design for clinical pharmacology studies (e.g., rBA/BE, DDI, special population,...Work at officeLocal areaWorldwide2 days per week3 days per week
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...Executive Director, Clinical Data Science At Eisai, satisfying unmet medical needs and... ...Clinical Data Science strategies for clinical studies and development plans across the... ...with industry best practices. Risk Management & Problem Solving: ~ Evaluate analytical...- ...Responsibilities Lead and manage clinical data management activities for oncology clinical trials, ensuring adherence to project timelines... ...direction to CRO clinical data management teams for assigned studies. Develop and implement data management plans, case report forms...Work at office
$28.6 - $44 per hour
Join to apply for the Oncology Clinical Data Manager role at Labcorp Join to apply for the Oncology Clinical Data Manager role at Labcorp Get... ..., and regulatory standards. Provide strategic insights into study protocol development, focusing on external data collection and...Full timePart timeCasual workReliefWork at officeFlexible hours- ...scientifically rigorous, decision‑relevant, and ready to support clinical studies, payer/HTA engagement, pricing, and reimbursement. With... ...scientific leadership to cross‑functional teams and executive management, serving as a trusted advisor on program risk, opportunity,...Full timeContract workWork at office
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