Clinical Research Coordinator — Trials & Compliance Lead
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Stanford University is seeking a Clinical Research Coordinator Associate to oversee the management and implementation of multiple research protocols at Stanford Hospital and Clinics. You will ensure regulatory compliance, assist with IRB submissions, consent processes, data collection, and CRF preparation, working with Principal Investigators. Responsibilities include recruitment, subject scheduling and follow-up, adverse event reporting, drug accountability, and maintaining study supplies, #J-18808-Ljbffr Stanfordlivetickets
- Stanford University in Stanford, CA, seeks a Clinical Research Coordinator Associate to manage multiple protocols, ensure regulatory compliance, and support IRB submissions. This on-site role works with the Stanford Hospital and Clinics, coordinating visits, data collection...Suggested
- Stanford Radiology is seeking a Clinical Research Coordinator 2 (CRC2) to support complex imaging studies... ...partners to coordinate multi-site trials, regulatory activities, data management... ...study progress, train staff, and ensure compliance with timelines and safety...Suggested
- Stanford University in Palo Alto is seeking a Clinic Clinical Research Coordinator Associate (CRCA) to coordinate oversight and implementation of neuromuscular... ...research protocols, ensuring efficiency and regulatory compliance. You will serve as the primary research liaison on...Suggested
- Stanford University is seeking a Clinical Research Coordinator II (CRCII) to conduct clinical research and independently manage complex studies... ...multiple studies, supervise staff, and ensure regulatory compliance under the CRM and PI supervision. The role may involve evenings...SuggestedWeekend workAfternoon shift
- .... Stanford University is seeking a Clinical Trial Regulatory lab manager (Clinical Trials... ...the administration and regulatory compliance of clinical research within SINC, and representing the... ..., participants, and study coordinators. This position is a 1-year fixed term...SuggestedFixed term contract
- Stanford University Department of Cardiothoracic Surgery, Division of Thoracic Surgery seeks a Clinical Research Coordinator Associate to coordinate moderately complex studies. The role supports principal investigators and residents in grant preparation, data management...Work at office
- ..., Inc. in Redwood City is seeking a Clinical Trial Manager to lead operational planning and delivery for assigned trials, ensuring GCP/ICH compliance and adherence to SOPs. You will collaborate... ...and at least 4 years in clinical research, with strong communication and...
$45 - $50 per hour
...Clinical Research Coordinator 1512819 ~ Hourly pay: $45-$50/hr ~ Worksite: Leading university (Palo Alto, CA 94304 - Hybrid) ~ W2 Employment... ...through regulatory compliance, data management, and sponsor... ...coordinating oncology treatment trials. ~ Experience supporting...Hourly payWork at office$157.59k - $203.94k
...Senior Clinical Trials Manager role leading global Phase I–IV clinical trial execution across therapeutic areas. Oversees study management teams,... ...operational strategy, timelines, budgets, and regulatory compliance while partnering with cross-functional stakeholders and...- ...Corcept Therapeutics seeks a Clinical Trial Manager to independently oversee medium to large... ...all clinical aspects, ensuring protocol compliance, GCP adherence, and successful study execution... ..., guidance, and oversight to Clinical Research Associates with regular performance...Contract work
- ...Cancer Institute (SCI) is seeking a Clinical Research Coordinator 2 to support neurology-related oncology... ..., manage data, ensure regulatory compliance, and collaborate with investigators across... ...staff, and coordination of complex trials, with responsibilities spanning budgeting...
- ...invites applications for a Clinical Research Coordinator 2 (CRC2) on a fixed-term 2-... ...complex industry-sponsored trials in ICU and OR settings, with... ...populations. You will lead recruitment, manage study data... ...investigators, ensure regulatory compliance, and support budget...Fixed term contract
- Stanford University in Stanford, CA seeks a Clinical Research Coordinator 2 (Fixed-term 2 years) to manage multiple complex industry-sponsored trials in ICU/OR, including sepsis, ARDS, and AKI. The CRC2 will recruit, collect data, and ensure protocol adherence across study...Fixed term contractNight shift
- ...Perioperative, and Pain Medicine seeks a Clinical Research Coordinator 2 (CRC2) for a fixed‑term 2‑year... ...coordinate complex industry‑sponsored trials in critical care and OR settings, recruit... ...Responsibilities include regulatory compliance, IRB interactions, budget development...Fixed term contract
$156.6k - $184.3k
...antagonists. With advanced clinical trials in patients with hypercortisolism... ...(when applicable) to ensure compliance with protocol and the... ...goals. May serve as a Study Lead to the multifunctional team... ...of data. Providing Clinical Research Associates with project‑specific...Full timeWork at office3 days per week$160k - $170k
...grow and develop their skills.The Sr. Clinical Trial Manager (Sr CTM) is responsible for effective... ....Review monitoring reports for compliance to study protocols, regulations and ICH... ...and EDC metrics reporting. Assist in coordinating study specific training or re-training...Full timeTemporary workWork experience placementWork at officeRemote workFlexible hours$34 per hour
...Assistant Clinical Research Coordinator 1503779 ~ Hourly pay: $34/hr ~ Worksite: Leading university (Palo Alto, CA 94304 - Hybrid) ~ W2 Employment, Group Medical, Dental... ..., and study operations while ensuring compliance with research protocols and regulatory requirements...Hourly payShift work3 days per week- Stanford University invites applications for a clinical research professional to support the Sean N. Parker Center for Allergy and Asthma... ...focuses on recruitment, data management, budgeting, regulatory compliance, and collaboration with investigators and sponsors to ensure...
- Ascendis Pharma, a global biopharmaceutical company, is seeking a Senior Clinical Trial Manager (Sr CTM) to lead global and regional clinical trials. The role is based in Palo Alto, CA or remote, reporting to the Director, Clinical Operations. Responsibilities include site...Remote job
$34.56 - $40.3 per hour
A leading medical institution is seeking a Cancer Clinical Research Coordinator Associate to oversee clinical studies in the Melanoma-Oncology area. This role entails serving... ...for research participants and ensuring compliance with protocols while managing critical research...Hourly pay$84.86k - $97.02k
A leading educational institution in California is seeking a Clinical Research Coordinator Associate for clinical research projects in pediatric oncology. This full-time, entry... ...studies, managing data, and ensuring compliance with research protocols. Ideal candidates...Full timeWork at office- Palo Alto Veterans Institute for Research (PAVIR) is seeking a Clinical Research Coordinator II to support day-to-day operations of one or more clinical studies. The role works closely with the Principal Investigator, sponsors, regulatory bodies, and participants to ensure...Full time
- Stanford University’s Skin Innovation and Interventional Research Group (SIIRG) in the Department of Dermatology is seeking a Clinical Research Coordinator Associate (CRCA) to coordinate clinical studies The CRCA will coordinate moderately complex aspects of one or more...
- Stanford University’s Stanford Center for Clinical Research (SCCR) is seeking a Clinical Research Coordinator Associate to support hospital medicine studies. The... ...close-out, manage patient interactions, and ensure compliance with protocols and regulatory requirements. The...
- Stanford University Department of Dermatology seeks an Assistant Clinical Research Coordinator to support data collection and coordination of clinical studies, including dermatology trials. The role operates under supervision of the principal investigator and research manager...
- Stanford University’s Department of Dermatology is seeking an Assistant Clinical Research Coordinator (ACRC) to perform administrative support duties related to the collection of clinical data and the coordination of clinical studies. The ACRC will support federal and non...
- Stanford University is seeking an Assistant Clinical Research Coordinator to provide administrative support for clinical data collection and study coordination. You will work under the supervision of the principal investigator and study coordinators, handling regulatory...
- Stanford University is seeking a Clinical Research Coordinator 2 to conduct clinical research and work independently on progressively more complex projects/assignments. Independently manage significant and key aspects of a large study or all aspects of one or more small...
$146.54k - $189.64k
...Operations plays a key role in ensuring that Gilead clinical trials are conducted in compliance with applicable SOPs, company policies and... ...ensure project team goals are met.With guidance, may lead contract research organization (CRO) and vendor selection and, where...Full timeContract workFor contractorsFor subcontractorInterim roleLocal areaFlexible hours$120k - $150k
...opportunity for an experienced Clinical Operations Professional who... ...managing Phase I-III clinical trials in an industry setting and a... ...be responsible for Contract Research Organization (CRO) oversight... ...on time, within budget and in compliance with Standard Operating Procedures...Full timeContract workFor contractorsInterim roleLocal areaWorldwide
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