Clinical Research Associate
ICON
Clinical Research Assoicate ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What You Will Do: You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively. Key responsibilities include: Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. Collaborating with investigators and site staff to facilitate smooth study conduct. Performing data review and resolution of queries to maintain high-quality clinical data. Contributing to the preparation and review of study documentation, including protocols and clinical study reports Your Profile: You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills. Required qualifications and experience: Bachelor's degree in a scientific or healthcare-related field. Minimum of 2 years of experience as a Clinical Research Associate. In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. Strong organizational and communication skills, with attention to detail. Ability to work independently and collaboratively in a fast-paced environment. Willingness to travel as required (approximately 60%) What ICON can offer you: Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: Various annual leave entitlements A range of health insurance offerings to suit you and your family's needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here #J-18808-Ljbffr
$115k - $140k
...What You Will Do You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants in... ...trials and respond to emergency situations based upon clinical research standards. Responsibilities Responsible for all aspects of study...SuggestedWork at officeLocal areaRemote workNight shift- ...IQVIA is seeking a Clinical Research Associate to ensure smooth operation of study sites and drive breakthrough research in oncology. You will perform site visits, assist with recruitment plans, provide protocol training, and maintain TMF/ISF documents while ensuring regulatory...Suggested
- ...Clinical Research AssociateTo be eligible for this position, you must reside in the same country where the job is located. Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol...SuggestedLocal area
- ...Description Experienced Clinical Research Associate - Sponsor Dedicated Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into...SuggestedContract workInterim roleLocal areaImmediate startRemote workFlexible hours
- ...SUMMARY: Under direction of the Manager of Grants & Special Projects, the Clinical Research Associate coordinates all aspects of clinical trials within the assigned unit.at the Adult Immunology Clinic, Highland Campus. In consultation with providers and other clinical...SuggestedFull time
- ...ICON plc is a world-leading healthcare intelligence and clinical research organization. We are seeking a CRA II to design and analyze clinical trials, interpret data, and contribute to innovative treatments and therapies. You will conduct site visits, ensure protocol compliance...
- ...Bring your monitoring expertise to the forefront of innovation. We are looking for a Clinical Research Associate (CRA) to join our A-team (remote; with travel). As a CRA at Allucent, you will independently control and monitor investigational sites, pro-actively detect...Work at officeRemote workFlexible hours2 days per week
- ...the frontline of medical science, changing lives, and bringing new medicines to those who need them. Job Description As a Clinical Research Associate you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of...Work visa
$85k - $130k
...an important member of the Alira Health Clinical team. The CRA is highly motivated and functions... ...with Lead CRAs, Sr CRAs, in-house CRAs, Associate Director of Clinical Monitoring and... ...AND LANGUAGES Knowledge of clinical research, ICH GCP and local regulations Knowledge...Contract workInterim roleLocal areaRemote workFlexible hours- ...AbbVie is seeking a Clinical Research professional to advance clinical trials by engaging investigators, training site staff, and monitoring site performance with a strong focus on data integrity and patient safety. You will partner with sites to ensure compliant trial...
$110.52k - $138.15k
...Oncology ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment... ..., or medicine. Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and...Work experience placementFlexible hours$92.32k - $126.94k
...that drive clear economic value, better clinical outcomes and improved quality of life for... ...CRA supports the day to day operations associated with the execution of clinical trials. He... ...of operational aspects of clinical research and regulatory regulations; Good interpersonal...Temporary workWork experience placementInterim roleWorldwide$100k
...subject protection is maintained, Good Clinical Practice (GCP), and applicable regulations... ...proficiency. Understanding of clinical research processes and regulations. Certifications such as Society of Clinical Research Associates (SoCRA) or Association of Clinical Research...Contract workInterim roleLocal areaRemote work- ...abbvie on LinkedIn, Facebook, Instagram, X and YouTube. Job Description Advance AbbVie's pipeline by striving for excellence in clinical research, turning science into medicine for our patients and leveraging new advanced capabilities to drive industry leading performance...Contract workTemporary workLocal area
- Location Portola Valley, San Mateo County Posted Aug 2026 About this position Position: Clinical Research Associate (CRA) Location: Redwood City, CA Length: 6 Month Contract Job Description: Were seeking a Clinical Research Associate (CRA) with strong clinical monitoring...Contract workInterim role
$90k - $110k
Avania is hiring Clinical Research Associates II (CRA II) - Medical Device Clinical Trials Salary range $90,000 - $110,000 + Annual performance related bonus + Benefits - Minimum 2+ years of prior CRA experience needed Avania's Clinical Research Associate II (CRA II)...- Abbott Laboratories in Alameda, California is seeking a Clinical Research Associate I to support clinical trials, monitor site activities, and ensure protocol compliance under supervision. You will collaborate with cross-functional teams, assist with data collection and...
$83.48k - $125.22k
About Karius Karius is a life science, venture-backed clinical metagenomics company, focused on elevating patient care through microbial... ...of education and experience. Three to five years of clinical research monitoring experience, including independent site management responsibilities...Interim roleWork at officeLocal areaRemote work- ...office. QT Imaging is a medical device company engaged in research, development, and commercialization of innovative body imaging... ...QT Imaging is seeking a motivated and detail-oriented Clinical Research Associate (CRA) to support the execution and management of clinical...Contract workPart timeInterim roleWork at officeRemote work
- JOB DESCRIPTION: Clinical Research Associate I Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to: Career development with an international company...Worldwide
$70 - $75 per hour
Sr. Field Clinical Research Associate Remote with Travel required in the North Central Region (ideally based out of Boston, MA or Philadelphia, PA) Hybrid role Compensation: $70 - $75 per hour ABOUT THE ROLE Our client, a leading life sciences company, is seeking a Sr....Hourly payContract workPart timeLocal areaRemote work$130k
Avania is hiring SeniorClinical Research Associate (Sr CRA) Salary Range up to $130,000 + Annual Performance related bonus + Benefits Avania's ClinOps Team establishes, maintains and supports clinical trials; as a key member of the team, our Sr CRA performs clinical...- ...Founded in 1995, PSI CRO is a privately owned, global Contract Research Organization with more than 3,000 employees dedicated to... ...PSI is the right place for you. Job Description As a Lead Clinical Research Associate, you'll provide leadership, oversight, and mentorship...Contract workRemote workWorldwideWork visa
- Alameda Health System seeks a Clinical Research Associate to coordinate all aspects of clinical trials at the Adult Immunology Clinic, Highland Campus. Under the Manager of Grants & Special Projects, you will select, implement and monitor trials, educate staff and enroll...
- Elanco seeks a Senior Clinical Research Associate (CRA) - Animal Health to lead and execute monitoring for farm and companion animal studies within the Global Clinical Development Sciences team, ensuring studies meet GCP/VICH standards and support regulatory approvals....
- Allucent is seeking a Clinical Research Associate (CRA) to independently monitor investigational sites, ensuring compliance with the trial protocol and GCP. The role is remote with travel across the United States, coordinating between sponsors and sites to maintain trial...Remote job
- ...Bio is seeking a Senior In-House CRA to oversee monitoring of clinical trials, coordinate with sites, CROs, and vendors, and ensure inspection... ...-friendly role reports to the Senior Clinical Trial Manager/Associate Director Clinical Operations and requires strong GCP, FDA, and...Remote job
$50k - $70k
...Summary The In-house CRA is an important member of the Alira Health Clinical team. In-house CRAs manage and support clinical sites from site... ...or equivalent experience 1-2 years of experience in clinical research Permanent authorization to work in the U.S. Languages English...Permanent employmentContract workLocal areaRemote workFlexible hours- Syneos Health is seeking a Clinical Research Associate - Full-Service to support remote monitoring of site activities across the United States. You will conduct site qualification, initiation, interim monitoring, and close-out visits, ensuring compliance with ICH-GCP and...Remote jobInterim role
- The Department of Digestive Diseases at UCLA is seeking a Staff Research Associate to support clinical studies in general gastroenterology, GI hemorrhage, and digestive diseases. You will collect and manage research data, maintain study databases, prepare reports, and...
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