Sr. Clinical Research Associate
$110.52k - $138.15kICON Strategic Solutions
Sr. Clinical Research Associate - West Coast 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 Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. What You Will Do You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement. Key Responsibilities Include Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution. Collaborating with cross‑functional teams to ensure timely and accurate data collection and reporting. Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct. Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations. Your Profile You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others. Required Qualifications And Experience Bachelor's degree in a relevant scientific discipline or healthcare‑related field Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements. Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem‑solving skills. Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex 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. Salary range: $110,520.00‑$138,150.00 Bonus, Com, Stock, Benefits & Disclaimer Verbiage Actual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill level. You may be eligible for a bonus, stock compensation and commissions in some cases depending on your role and performance. 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
$109.5k - $153.3k
...As an investigator site facing role, the Sr. CRA will act as a customer advocate through... ...corporate goals. Organize and maintain clinical study documentation (e.g., Trial Master... ...preferred. Minimum of five (5) years of clinical research monitoring experience (including pre-...SeniorFor contractorsLocal areaRemote work- ...Direct message the job poster from Integrated Resources, Inc ( IRI ) Lead Recruiter at Integrated Resources Inc. (IRI) Sr Clinical Research Spec 100% remote in CA/MN 12 Months+ Preferred location(s): Santa Rosa, CA / Northern California - Bay Area / Plymouth...SeniorContract workRemote work
- ...A renowned clinical research organization in California is looking for a Clinical Research Associate to oversee monitoring activities for clinical sites. Responsibilities include conducting various types of monitoring visits, preparing monitoring reports according to regulatory...SeniorLocal areaRemote work
$110.52k - $138.15k
...Senior Clinical Research Associate – Oncology – Southern California ICON plc is a world‑leading healthcare intelligence and clinical research organization... ...mission to shape the future of clinical development. The Sr. Clinical Research Associate (Sr. CRA) will be responsible...SeniorWork experience placementInterim roleLocal areaRemote workFlexible hours- AbbVie in South Chicago Heights, Illinois is hiring for a role focused on advancing clinical research excellence through effective collaborations and adherence to high-quality standards. As a primary point of contact, you will engage with site staff and investigators to...Senior
$97k - $193k
Worldwide Clinical Trials Holdings, Inc. is looking for a Clinical Research Associate with 5+ years of experience and a solid background in CNS/Neurology. The role involves managing clinical research projects, ensuring compliance, and training sites. Strong organizational...SeniorWorldwide- ...Responsibilities include monitoring activities for assigned clinical sites, both in person and remote, including planning and execution... ...of education and experience. Experience Requirements > 5 years of experience as a Clinical Research Associate. #J-18808-Ljbffr ProPharmaSeniorInterim roleWork at officeLocal areaRemote work
$97k - $193k
Responsibilities Managing research activities at sites participating in Worldwide’s clinical research projects. Involved in all stages of the clinical study, including... ...5+ years of experience as a Clinical Research Associate. 4‑year university degree or Nursing degree....SeniorRemote jobWork at officeWorldwide- ...investigators and verifies that the investigator has adequate qualifications, resources, facilities, equipment and staff to conduct the clinical study throughout the study period. Trains investigational site staff as necessary When applicable, supports preparation of...SeniorInterim roleRemote work
- ICON Strategic Solutions is seeking a Sr. Clinical Research Associate for the West Coast to manage clinical trial activities, ensuring compliance with protocols and regulatory requirements. You will be responsible for monitoring trial sites, conducting site visits, and...Senior
- .... As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol... ..., nursing, or medicine. Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and...SeniorRemote workWorldwide
- ...We are looking for a FREELANCE, PART-TIME CRA to strengthen our clinical operations team in Ventura, Illinois & Ohio! Job Requirements... ...of onsite monitoring activities Profound knowledge of clinical research processes and medical terminology Expert knowledge of ICH GCP,...Part timeFreelanceLocal areaRemote work
- ...Responsibilities Manage day-to-day operational execution of assigned clinical studies to achieve study milestones, quality expectations, and... ...credentials preferred. Typically requires 5+ years of clinical research or pharmaceutical industry experience, including 2+ years of...
$91.34k - $114.17k
...Clinical Research Associate - Multi Therapeutic Area (Early Development) - West Region What You Will Be Doing Serve as the primary point of contact between investigational sites and the sponsor Conduct all types of site visits, including selection, initiation, routine...Work experience placementLocal areaVisa sponsorshipFlexible hours- ...We are hiring in Chicago, Southern California & NY (Northeast). 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 areaRemote work
- ...Job Description: Conduct site monitoring visits (initiation, routine, and close-out) to ensure compliance with the clinical protocol, GCP, and regulatory requirements. Assist in the preparation and review of essential trial documents, such as informed consent forms, case...Work at office
$71.9k - $189k
...Clinical Research Associate, Sponsor Dedicated California, United States of America | Full time | Field-based | R1541733 To be eligible for this position, you must reside in the same country where the job is located. Essential Functions Perform site monitoring visits (...Full timePart timeLocal areaImmediate startWorldwide$90k - $130k
...FL, GA, KS, MA, MD, MI, NC, OH, OK, TN, TX, WA Vanguard Clinical, Inc. is a Contract Research Organization (CRO) headquartered in San Diego, CA. Our... ...clinical data at assigned sites. The Clinical Research Associate (CRA) will execute monitoring responsibilities for clinical...Permanent employmentFull timeContract workInterim roleWork at officeRemote workFlexible hours- Join our team and use your skill with an organization known nationally for excellence in research! The Clinical Research Associate I works under the direction of a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or other supervising staff...Daily paidLocal area
- Cedars-Sinai Medical Center is looking for a Clinical Research Associate I in California to support the implementation of noncomplex research studies. The role involves collecting and evaluating clinical research data, assisting in the prescreening of research participants...
- ICON Strategic Solutions is seeking a Clinical Research Associate for the West Region to serve as the primary contact between investigational sites and the sponsor. The ideal candidate will have a Bachelor’s degree in Life Sciences and 2+ years of on-site monitoring experience...
- Clinical Research Associate - Full-Service Syneos Health is a fully integrated biopharmaceutical solutions organization focused on accelerating customer success and improving patient outcomes. Job Responsibilities Perform site qualification, site initiation, interim monitoring...Interim roleLocal areaImmediate startRemote workFlexible hours
- Cedars-Sinai is seeking a Clinical Research Associate I to join their team in Missouri. The role involves assisting in the coordination and implementation of research studies, including data collection and IRB submissions. The ideal candidate will have a High School Diploma...
$90k - $120k
Clinical Research Associate job at Piper Companies. California. Piper Companies is seeking Clinical Research Associates to join a highly accredited CRO. This position is fully remote but does require on-site monitoring in Canada. The Clinical Research Associate will take...Remote work- Direct Jobs is seeking a Clinical Research Associate I in California, Missouri, to assist with the coordination and implementation of noncomplex research studies. Key responsibilities include collecting and evaluating data, scheduling research participants, and assisting...
- Clinical Research Associate 3 job at V R Della Infotech Inc. California. Senior Clinical Research Associate (In-House in Sunnyvale & Field Role)... ...Fluorescence Imaging Clinical Team, and other team members. The Sr CRA will also travel frequently to Investigational Sites to...Interim roleWork at officeRemote workShift work3 days per week
- IQVIA Argentina is seeking a Clinical Research Associate to provide on-site monitoring and ensure adherence to clinical and regulatory standards. Candidates must have at least 2 years of experience and a Bachelor's degree in a relevant field. The role involves collaborating...
- Initial Therapeutics, Inc. is looking for a Clinical Research Associate to join our team in California. The role involves ensuring effective site engagement and maintaining regulatory compliance in clinical trials. You will be the main point of contact for investigative...
- A global clinical research organization is seeking a part-time Freelance Clinical Research Associate (CRA) to join their team. The role involves monitoring clinical trials, ensuring compliance with regulations, and maintaining data integrity. The ideal candidate should...Part timeFreelance
- BoneSource is seeking a Clinical Research Associate I in California, Missouri to assist in coordinating noncomplex research studies. This role includes tasks like data collection, scheduling research participants, and compliance with IRB submissions. Ideal candidates have...
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Sr. Clinical Research Associate. Be the first to apply!
- clinical research assistant California, MO
- clinical research associate cra California, MO
- senior clinical research associate California, MO
- on-site clinical research associate (traveling/remote) California, MO
- clinical research associate California, MO
- clinical research administrator California, MO
- clinical trials assistant California, MO
- senior data management analyst California, MO
- senior app developer California, MO
- senior game producer California, MO

