Average salary: $139,606 /yearly
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$71.5k - $142.5k
...is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the...SuggestedHourly payFull timeContract workWork at officeRemote workWorldwideFlexible hours$95k - $125k
...is responsible for the initiation and independent oversight of clinical centers to ensure the successful conduct of active clinical studies... ...clinical study centers for participation in Inspire clinical trials. Serve as a primary point of contact for study sites,...SuggestedWork experience placementLocal areaRemote workFlexible hours$112.15k - $168.23k
...into faster access to life-changing medicines for patients? As a Clinical Research Associate, you will be the face of AstraZeneca at... ...efficient, cost- and time-optimized delivery of quality clinical trials; apply risk-based thinking to streamline processes and improve...SuggestedHourly payFull timeTemporary workLocal areaRemote work- ...Clinical Research Assistant Works under direct supervision and assists research coordinators with organizing, gathering and compiling... ...for staff and all researchers participating in clinical trials in accordance with IRB regulations. May provide clerical and technical...SuggestedWork at officeLocal areaRemote workShift work
- ...Pulse Biosciences is seeking a Senior Clinical Research Associate to manage and monitor soft tissue ablation trials in the U.S. remote setup. The Sr. CRA will support study planning, site startup, patient recruitment, data quality, and regulatory compliance with CFR FDA...SuggestedRemote work
- ...Syneos Health in Germany is seeking a CRA I to join our clinical solutions team. This role supports site qualification, initiation, monitoring, and close-out visits, performed on-site or remotely, to ensure regulatory and ICH-GCP compliance. You will verify informed consent...SuggestedRemote work
- A large financial institution is seeking a remote CRA Program Support Specialist to assist in the Community Reinvestment Act (CRA) initiatives. This role involves collaborating with internal teams, supporting CRA compliance examinations, and analyzing performance data. ...SuggestedRemote work
- ...CRA for Germany (remote across Leipzig/Halle/Berlin) to monitor clinical sites. The role requires fluency in German and English, good... ...activities, ensuring data integrity and patient safety throughout the trial. The candidate will collaborate with sponsor teams, review ISF/...SuggestedRemote work
- Description Experienced Clinical Research Associate - Sponsor DedicatedSyneos Health is a leading fully integrated biopharmaceutical solutions... ...and completeness. Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator/physician site is...SuggestedContract workInterim roleLocal areaImmediate startRemote workFlexible hours
$225k - $270k
...of Individual Case Safety Reports (ICSRs) Perform comprehensive medical review of Individual Case Safety Reports (ICSRs) from clinical trials and post-marketing sources. Assess the clinical significance, seriousness, expectedness, and causality of adverse events...SuggestedRemote workFlexible hours- ...within the Peredo Lab in the Department of Special Education at Vanderbilt University. This individual will support an NIH Phase 1 clinical trial investigating a naturalistic developmental behavioral intervention (NDBI) approach for Latino families. The Research Assistant...SuggestedFull timeContract workWork at officeRemote workFlexible hoursDay shift
- Job Description CANDIDATE MUST RESIDE IN ONE OF THE FOLLOWING LOCATIONS AND BE FLUENT IN SPANISH : South Florida - Ft. Lauderdale, Miami, Boca Raton, Key LargoThe role is accountable for performance and compliance for assigned protocols and sites in a country.Under the ...SuggestedRemote work
- ...Syneos Health is recruiting for a CRA II to support multisponsor clinical monitoring across Germany with a focus on the north-east region. The role involves on-site or remote monitoring, site qualification and initiation, overseeing data quality, and ensuring regulatory...SuggestedRemote work
- ...Associate Clinical Research SpecialistLocation: Irvine, CA (Hybrid, 50% onsite, 50% remote) Duration: 16+ months contract with the possibility... ...of MS Office Suite and Clinical Systems such as CTMS (Clinical Trial Management System), eTMF (electronic Trial Master File)Good...SuggestedContract workWork experience placementImmediate startRemote work
$80k - $99k
...there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special...SuggestedFull timeContract workWork at officeRemote workWorldwideFlexible hours- ...Syneos Health, Inc. is seeking a Clinical Monitoring/CRA to support site management, monitoring, and data integrity across sponsor studies... ...travel up to 75%. Knowledge of GCP/ICH guidelines is essential for audit readiness and successful trial delivery. #J-18808-LjbffrRemote work
$117k - $184.2k
...country or a cluster.Responsibilities:Main Point of Contact (POC) for assigned protocols and link between Country Operations and clinical trial team (CTT).Responsible for project management of the assigned studies: pro-actively plans, drives and tracks execution and...Full timeFor contractorsLocal areaRemote workFlexible hours$180k - $210k
...Who We Are Emerald Clinical Trials is a global leader in clinical research, partnering with over 160 biotech companies and 15 of the world's top 20 pharmaceutical firms. Headquartered in Singapore, we combine scientific excellence with operational expertise to...Full timeLocal areaRemote workWorldwide- ...Clinical Research Associate Advance AbbVie's pipeline by striving for excellence in clinical research, turning science into medicine... ...effective engagements positioning AbbVie as the choice in clinical trials. Focus on site clinical research that ensures appropriate...Contract workLocal areaImmediate startRemote work
- ...Supporting Clinical Operations in a remote full-time capacity, the Clinical Trials Assistant will manage essential documents for clinical trials, assist with study drug release, and participate in investigator meetings while ensuring compliance with regulatory guidelines...Full timeRemote work
- ...candidates with PhDs and/or Post-Doctoral Researchers with Gastrointestinal (GI) experience for a full-time,office-basedAssociate Clinical Trial Manager (aCTM) position in our Cincinnati, OH office. The aCTM is part of the Clinical Trial Management team working with...Full timeContract workWork at officeWork from home
- ...we are currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team in our Dallas office. The aCTM will be a part of the Clinical Trial Management...Full timeContract workWork at officeWork from home
- ...Clinical Research Associate II - Medical Device Clinical Trials Avania's Clinical Research Associate II (CRA II) establishes, maintains and supports clinical trials. Through the monitoring process, you will verify that the rights and well-being of human subjects are...Work experience placementRemote workFlexible hoursNight shift2 days per week3 days per week
- Vitalief is seeking a Research Office Assistant to support a long-term NIH-funded study focused on women with Alcohol Use Disorder. The role involves assisting with participant care, regulatory compliance, and study coordination in Newark, NJ, with some remote days as ...Work at officeRemote work
- ...As a Clinical Research Associate you will be responsible for a variety of monitoring tasks and you will have a chance to work on clinical... ...in different therapeutic indications, ensuring the clinical trial is conducted in compliance with study protocol and procedures,...Contract workWork from home
$80k - $110k
...Clinical Research Associate IISystImmune is seeking a high quality, ambitious and experienced Clinical Research Associate II (CRA II) to support SystImmune's clinical trials. The CRA II is responsible for the management and oversight of their assigned clinical study sites...Contract workInterim roleWork at officeLocal areaRemote work- ...elevate others.The CRA is an important member of the Alira Health Clinical team. The CRA is highly motivated and functions independently to conduct site monitoring responsibilities for clinical trials; as well as providing oversight, leadership, and guidance in the management...Contract workInterim roleLocal areaRemote work
- ...Clinical Study CoordinatorPrimary responsibilities of the positionServes as a primary contact between the company and study sites. Coordinates... ...related areas.Minimum 2 years working experience of clinical trials with IVD company; other devices or pharmaceutical clinical...Work experience placementWork at officeLocal area
$60k - $80k
...are searching for talented and passionate people who want to help shape the future of veterinary care. About the position The Vet Clinic Implementation Associate at Vetcove is responsible for overseeing the end‑to‑end management of large‑scale projects that enhance the...Hourly payFull timeRemote workHome office- ...Clinical Research Associate (CRA) for Beckman Coulter DiagnosticsThe Clinical Research Associate (CRA) for Beckman Coulter Diagnostics... ...templates (e.g., study guides, study tools/worksheets) and ensure Trial Master File (TMF), Sponsor Site Files (SSF), and Investigator...Contract workWork experience placementWork at officeRemote work

