Oncology Clinical Research Associate II — Site Partner
Initial Therapeutics, Inc.
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 sites, training site staff, and mentoring junior associates. Ideal candidates will have at least one year of clinical research experience and strong cross-functional collaboration skills. We offer comprehensive benefits, including medical/dental insurance and a 401(k) plan. #J-18808-Ljbffr Initial Therapeutics, Inc.
- ...therapeutic areas including immunology, oncology, and neuroscience, as well as... ...by striving for excellence in clinical research, turning science into medicine for... ...industry‑leading performance. Partners with the investigator and site staff for meaningful and effective...WebsiteContract workTemporary workLocal 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... .... CRA) will be responsible for performing investigative site management and monitoring activities throughout the...WebsiteWork experience placementInterim roleLocal areaRemote workFlexible hours$90k - $120k
Clinical Research Associate job at Piper Companies. California. Piper Companies is seeking Clinical Research... ...is fully remote but does require on-site monitoring in Canada. The Clinical... ...concentration. Strong experience in onsite oncology monitoring. Phase 1 oncology required....WebsiteRemote work- ...full service mid-sized CRO specialising in Oncology and Rare Disease. Since its foundation... ...’s lives. Responsibilities Performs on-site or remote Pre-Study, Initiation, Interim,... ...facilities, equipment and staff to conduct the clinical study throughout the study period....WebsiteInterim roleRemote work
- ...you will oversee and manage clinical trial activities to ensure they... ...Monitoring clinical trial sites to ensure adherence to study... ...experience as a Clinical Research Associate, with a strong understanding... ...Ohio) - near a major airport. Oncology monitoring experience...WebsiteRemote workWorldwide
$91.34k - $114.17k
...Clinical Research Associate - Multi Therapeutic Area (Early Development) - West Region... ...between investigational sites and the sponsor Conduct all... ...Collaborate with cross‑functional partners including CTAs, LTMs, and... ...monitoring early development Phase I/II clinical studies, across...WebsiteWork experience placementLocal areaVisa sponsorshipFlexible hours- Clinical Research Associate - Full-Service Syneos Health is a fully integrated biopharmaceutical solutions... ...outcomes. Job Responsibilities Perform site qualification, site initiation, interim... ..., act as Site Management Associate II and support site activities throughout...WebsiteInterim roleLocal areaImmediate startRemote workFlexible hours
- ...to-day operational execution of assigned clinical studies to achieve study milestones, quality... ...feasibility assessments, country and site selection, vendor selection, system set-up... ...Typically requires 5+ years of clinical research or pharmaceutical industry experience, including...Website
- ...FREELANCE, PART-TIME CRA to strengthen our clinical operations team in Ventura, Illinois &... ...activities Profound knowledge of clinical research processes and medical terminology Expert... ...all aspects of the clinical monitoring and site management process Conducting remote and...WebsitePart timeFreelanceLocal 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...WebsiteWork 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... ...country where the job is located. Essential Functions Perform site monitoring visits (selection, initiation, monitoring and...WebsiteFull timePart timeLocal areaImmediate startWorldwide$90k - $130k
...TN, TX, WA Vanguard Clinical, Inc. is a Contract Research Organization (CRO)... ...internally and as a partner to our Sponsor... ...management of clinical sites and monitoring of clinical... ...Clinical Research Associate (CRA) will execute... ...experience with oncological trials strongly...WebsitePermanent employmentFull timeContract workInterim roleWork at officeRemote workFlexible hours- ...and Central County. Laboratory Technician II is the journey-level position in this classification... ...Laboratory Information System—and assist Clinical Laboratory Scientists with testing in... ...for transportation from collection sites to main laboratory and receives specimens...WebsiteFull timeWork at officeLocal area
- ...IRI ) Lead Recruiter at Integrated Resources Inc. (IRI) Sr Clinical Research Spec 100% remote in CA/MN 12 Months+ Preferred location... ...project management responsibilities for selected studies and site management activities as needed. This role utilizes their...WebsiteContract workRemote work
$110.52k - $138.15k
...Sr. Clinical Research Associate - West Coast ICON plc is a world‑leading healthcare intelligence and clinical research organization. We’re proud... ...improvement. Key Responsibilities Include Monitoring clinical trial sites to ensure adherence to study protocols, regulatory...WebsiteWork experience placementFlexible hours$109.5k - $153.3k
...responsibilities of the role As an investigator site facing role, the Sr. CRA will act as a... ...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-...WebsiteFor contractorsLocal areaRemote work- 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...Website
- ...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...WebsiteLocal areaRemote work
- The County of San Mateo is hiring a Family Partner Support Specialist I/II in California. This role supports families navigating behavioral health systems, emphasizing peer support and education, and requires fluency in Spanish. Ideal candidates have lived experience in...Full timeAfternoon shift
- ...Heights, Illinois is hiring for a role focused on advancing clinical research excellence through effective collaborations and adherence to... ...standards. As a primary point of contact, you will engage with site staff and investigators to ensure successful trial conduct and...Website
$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... ...projects, ensuring compliance, and training sites. Strong organizational skills and ability to work...WebsiteWorldwide- 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...Website
- ...include monitoring activities for assigned clinical sites, both in person and remote, including... ...teams, Sponsor teams, and external partners involved in execution of the trial.... ...> 5 years of experience as a Clinical Research Associate. #J-18808-Ljbffr ProPharmaWebsiteInterim 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....WebsiteRemote jobWork at officeWorldwide- Clinical Research Associate 3 job at V R Della Infotech Inc. California. Senior Clinical Research Associate... ...travel frequently to Investigational Sites to conduct co‑monitoring along with... ...at the participating clinical sites. Partner with data management (CRO) to help the...WebsiteInterim roleWork at officeRemote workShift work3 days per week
- ICON Strategic Solutions is seeking a Sr. Clinical Research Associate for the West Coast to manage clinical trial activities, ensuring compliance... ...requirements. You will be responsible for monitoring trial sites, conducting site visits, and providing support to ensure trial...Website
- 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...WebsitePart timeFreelance
- Escarraga's Luxury Cleaning in California is seeking partners for its floor care services, requiring operational autonomy and specialized... ...insurance, and a professional approach to operations, including site protection and equipment management. Opportunities are project-based...Website
$115k - $140k
Fortrea in California is looking for a Sr. CRA 2 with at least 4 years of Clinical Monitoring experience and strong expertise in Oncology monitoring. The role involves all aspects of study site monitoring, including pre-study visits, ensuring regulatory compliance, and...WebsiteRemote job- ...Partner Program Manager We are seeking a motivated and experienced Partner Program Manager to join our dynamic team. In this pivotal role... ...to individuals unable to submit an application through this site because of a disability. Contact ****@*****.***...WebsiteTemporary workFlexible hours
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