Average salary: $119,849 /yearly
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- ...Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinical development program. The AD provides statistical strategies for the clinical trials and regulatory submissions and is accountable for the statistical deliverables within...SuggestedInterim role
- ...Job Description Responsible for providing Clinical Research support for all clinical trials. Under the direction of supervisor or designee, this position will serve as support for the clinical study team. Essential Duties And Responsibilities Participate...Suggested
- ...Clinical Research Associate The Clinical Research Associate for Beckman Coulter Diagnostics is responsible for supporting clinical activities to generate clinical evidence that will support product registration and/or product market clearance/approval. This position...SuggestedRemote work
- ...SUMMARY The Clinical Research Coordinator (CRC) is responsible for the coordination of daily clinical trial activities. USRC has a research Partnership with the principal investigator (PI) and their physician practice. The local oversight and direction for activities...SuggestedFull timePart timeWork at officeLocal area
- ...A leading clinical research organization is seeking a Clinical Research Associate to manage site monitoring responsibilities and ensure... ...and fluency in English, with preferred experience in clinical trials. This role requires a commitment to delivering high-quality results...Suggested
$60.41k - $65k
...Job Summary: The Clinical Research Associate I (CRA I) will join a team of experienced associates and manage various research trials, including first in human through phase 3 trials. The role will be expected to manage 2-3 studies simultaneously. The will ensure compliance...SuggestedFull timeWork at officeMonday to FridayFlexible hoursAfternoon shift$20.16 - $29.01 per hour
...A prominent healthcare institution located in Boston is seeking a Clinical Research Associate to enroll patients in clinical studies. The role involves coordinating with clinical teams, managing data submissions, and ensuring compliance with institutional protocols. Ideal...SuggestedHourly pay- ...Title: Clinical Research Associate (CRA) - B Location: San Diego, CA Duration: 8 Months 100% Onsite RESPONSIBILITIES: Carry out assigned functions applying knowledge and skill in an accurate, timely manner. Apply knowledge of FDA regulations to site...SuggestedTemporary workInterim roleFlexible hours
- ...Responsibilities: Excellent employment opportunity for a Clinical Research Associate in the South San Francisco area.... ...issues. May be asked to assist in the training of Clinical Trial Assistants. May conduct site evaluations/initiations and closeout...SuggestedContract work
- ...Responsibilities Primary point of contact for investigative site, providing contextual information on clinical trials and connecting stakeholders. Align, train, and motivate site staff and principal investigator on the goals of the clinical trial program, protocol, and...SuggestedContract workTemporary workLocal areaRemote work
$48k
...Overview Responsible for pre-clinical trial set up, initial and ongoing regulatory submission and IRB activities, subject screening and enrollment, specimen collection and transmittal, data collection and management, adverse event management to ensure protocol compliance...SuggestedLocal area- ...Job Summary: Coordinate various research trials for the Institute for Global Health, including early or late phase FDA-regulated trials... ...regulatory agencies. Enroll, register and screen patients for clinical research trials; collect and submit clinical trial patient data...SuggestedWork at officeMonday to Friday
- The Clinical Research Associate (CRA) position represents an opportunity to grow within an emerging medical device company. Solid knowledge... ...this requirement.) Prior experience in neurology clinical trials is strongly preferred Proficiency in Microsoft suite of...SuggestedFlexible hours
- * Design and implement consistent processes for clinical research and clinical trial infrastructure from the application stage through study startup to closeout and reporting.* Manage departmental space needs across vision science research labs, research faculty, and clinical...Suggested
$42k - $63k
...Position Summary Responsible for assisting UNMC Clinical Research Coordinators and Principal Investigators as needed in... ...project management, coordination, and implementation of clinical trials. Provide clinical, laboratory, and administrative support to the...SuggestedFull timeTemporary workWork at officeRemote work$55.89k - $65k
Posting Information Department: LCCC - Clinical Trials-426806 Career Area: Research Professionals Is this an internal only recruitment? No Posting Open Date: 03/24/2026 Application Deadline: 04/14/2026 Position Type: Permanent Staff (SHRA) Position Title: Soc/Clin...Permanent employmentFull timePart timeWork at officeMonday to FridayAfternoon shift$120k - $145k
...Program. To enable cancer and population sequencing, Personalis' Clinical Laboratory was built with a focus on clinical accuracy, quality... ...Familiarity with Electronic Data Capture (EDC) platforms and Trial Master File (TMF) organization and structure. Experience with...Full timeRemote work- ...medicine through cutting-edge research. Come join us as a Clinical Research Associate I. If you are adaptable, independent, and... .... Medical Record, Health Information Systems, clinical trials exposure or related health field. City of Hope employees...Work experience placement
$45 - $50 per hour
...Currently seeking a Clinical Research Associate in Alameda, CA. Details for the position are as follows: Job Description: ~ Pay: $45-50/hr. ~ Travel: 30-50% ~6-month assignment with possibility for extension or conversion based on performance...$70k - $110k
...Job Description About the Role The Clinical Research Associate (CRA) is primarily responsible for ensuring the rights and wellbeing of trial participants are protected and the reported trial data are accurate, complete, and verifiable from the source documents....Local areaFlexible hours- ...monitoring, closure, and management of sites participating in clinical research studies sponsored by Glaukos. The SR. Clinical Research... ...Verify and reconcile site's essential documents against the trial master file as required Oversee and conduct monitoring activities...Work experience placementInterim roleWork at officeRemote workNight shift
- ...Job Title: Clinical Research Associate Location: Los Angeles, CA 90025 Duration: 13 weeks Shift: Schedule: Day 5x8-Hour... ...necessary to ensure adequate funding throughout the course of the trial. • Ensures timely filing of annual renewals and amendment...Contract workRemote workShift work
- ...week. If hired you must reside in the commutable area. The Clinical Research Associate I works under the direction of a Clinical Research... ...of potential research participants for various clinical trials. Schedules research participants for research visits and research...Local area
- ...Document site progress and escalate risks or issues to the clinical team Assist in tracking site budgets and ensuring timely site... ...pharmaceutical or CRO industry Experienced monitoring oncology trials required. Proficient in ICH-GCP, local regulatory requirements...Local areaRemote workVisa sponsorship
- ...Clinical Research Associate Step into a role where your work directly supports groundbreaking therapies that can transform the lives... ...and organize administrative aspects of assigned clinical trials Support monitoring visit scheduling and report review Prepare...Work experience placementWorldwide
- ...Associate Clinical Trial Manager Medpace is a leading CRO for Biotech companies and we are currently seeking candidates with PhDs and/or Post-Doctoral Research experience within Metabolic research for a full-time office-based Associate Clinical Trial Manager (aCTM)...Full timeContract workWork at officeLocal areaImmediate startFlexible hours
- ...diseases, shaping the future of medicine through cutting-edge research. We are seeking a highly skilled and detail-oriented Clinical Research Associate II to manage multiple research protocols with a focus on efficiency, regulatory compliance, and study oversight...Work experience placement
- ...Industry: Medical Devices Title: Clinical Research Associate III Job ID: ISIJP00011794 Location: Sunnyvale CA (Hybrid: 3... ...candidate will have in-depth knowledge of clinical research in drug trials, including Good Clinical Practice (GCP) and relevant US...Contract workInterim roleWork at officeRemote workShift work
- ...lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical... ...Identify if any untrained staff are participating in Clinical trial activities, document and communicate the issues and suggested...Contract workFlexible hoursNight shift
- ...Job Summary Under general supervision, the clinical research associate (CRA) will be responsible for oversight of clinical trials for the SLU School of Medicine. Responsibilities include screening, recruiting and enrolling subjects, conducting subject research visits...Work experience placementWork at office

