Clinical Study Lead (Sr. Clinical Research Associate)
$120k - $130k6AM City
Job Description Salary: $120-130K Company Summary: A global, specialty pharmaceutical group with an impressive track record is seeking a motivated Clinical Study Lead for a hybrid role in San Francisco (Palo Alto). Their commercial supply of pharmaceutical products generated $83m in revenue in FY2023 (a 24% uptick from the year prior during a year of record layoffs). Since their first clinical trials in 2006, they've had 3 approvals already on the market. Currently, they have 6 indications in Phases II and III, so they are looking for a driven, growth-oriented Clinical Study Lead to drive their pipeline forward. ***** Candidate must be based in SF to be considered.***** The Clinical Study Lead will be responsible for: Leading in house study activities for a large global Phase 3 study Mentoring junior team members Overseeing the set‑up and maintenance of study systems which may include Clinical Trial Management System (CTMS), Trial Master File (TMF), study SharePoint etc. Reporting into the Clinical Program Lead May be responsible for CRA and CTAs as direct reports An ideal candidate for this role MUST have: 5+ years of sponsor/CRO experience 3+ years of on‑site monitoring experience 2+ years of experience leading studies or trials in house (rare disease or derm preferred) At least 2 years of experience managing direct reports or mentoring junior clinical operations team members A Bachelor's degree in Biological Sciences, Nursing, Pharmacy or a related discipline A working knowledge of ICH GCP guidelines Benefits: Competitive salary with benefits High degree of commercial exposure early in your career Being a part of team whose work directly aims to improve the quality of people's lives Great work‑life balance If you are interested in this Clinical Study Lead role, don't hesitate to reach out! #J-18808-Ljbffr
$100k - $125k
Clinical Research Associate (Sr.) job at EPM Scientific - San Francisco County, CA *** MUST BE LOCAL TO CA OR NY STATE - NO EXCEPTIONS *** Salary... ...Clinical Research Associate to facilitate their in house studies. Responsibilities Managing and investigating clinical trials...SeniorLocal area$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 to foster an inclusive... ...Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good...SeniorWork experience placementFlexible hours$109.5k - $153.3k
...investigator site facing role, the Sr. CRA will act as a customer advocate through a study life cycle. Understand and... ...corporate goals. Organize and maintain clinical study documentation (e.g., Trial... ...of five (5) years of clinical research monitoring experience (including...SeniorFor contractorsLocal areaRemote work- EPM Scientific, a leading global pharmaceutical group, is seeking a Clinical Research Associate (Sr.) for a hybrid role in San Francisco. You will manage clinical trials, coordinate... ...with guidelines while supporting crucial studies aimed at improving healthcare. This role...SeniorLocal area
- ...include monitoring activities for assigned clinical sites, both in person and remote,... ...parameters. Ex-US: Potentially perform study startup activities in accordance with local... ...Requirements > 5 years of experience as a Clinical Research Associate. #J-18808-Ljbffr ProPharmaSeniorInterim roleWork at officeLocal areaRemote 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
- ...ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted... ...trial sites to ensure adherence to study protocols, regulatory requirements, and... .... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical...SeniorRemote workWorldwide
- 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...SeniorRemote jobLocal area
$110.52k - $138.15k
Senior Clinical Research Associate - Oncology - Southern California ICON plc is a world‑leading healthcare intelligence and clinical research organization. We’re proud to foster... ...shape the future of clinical development. The Sr. Clinical Research Associate (Sr. CRA) will...SeniorWork experience placementInterim roleLocal areaRemote workFlexible hours$110.52k - $138.15k
Senior Clinical Research Associate - Oncology - Southern California ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster... ...shape the future of clinical development. The Sr. Clinical Research Associate (Sr. CRA) will...SeniorWork experience placementInterim roleLocal areaRemote workFlexible hours$71.9k - $189k
...Clinical Research Associate, Sponsor Dedicated California, United States of America | Full time | Field... ...predictability. Administer protocol and related study training to assigned sites and... ..., managers, and clients. IQVIA is a leading global provider of clinical research services...Full timePart timeLocal areaImmediate startWorldwide- ...with an organization known nationally for excellence in research! The Clinical Research Associate I works under the direction of a Clinical Research... ...the coordination/implementation of noncomplex research studies. Supports objectives of research studies through noncomplex...Daily paidLocal area
$90k - $140k
...Overview We are hiring a Clinical Research Associate II or Senior Clinical Research Associate with Major... ...monitoring visit activities, inclusive of all study visit types (PSV, SIV, IMV and COV)... ...with oversight from the Clinical Team Lead role Provide feedback to assist sites...Hourly payRemote work- ...IQVIA Argentina is seeking a Clinical Research Associate to provide on-site monitoring and ensure adherence to clinical and regulatory standards.... ..., managing site practices, and ensuring quality throughout study execution. The company offers competitive compensation based...
- ...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...
$90k - $120k
...Clinical Research Associate job at Piper Companies. California. Piper Companies is seeking Clinical Research Associates to join a highly accredited... ...guidelines. Support subject recruitment plans and provide study-specific training to site staff. Manage regulatory submissions...Remote work- ...FREELANCE, PART-TIME CRA to strengthen our clinical operations team in Ventura, Illinois &... ...activities Profound knowledge of clinical research processes and medical terminology Expert... ...rights and safety of patients involved in a study are protected Performing and coordinating...Part timeFreelanceLocal areaRemote work
$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... ...monitoring early development Phase I/II clinical studies, across multiple therapeutic areas Proficient in ICH‑GCP,...Work experience placementLocal areaVisa sponsorshipFlexible hours- ...Overview Experienced Clinical Research Associate - Full-Service Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate... ...support the effective conduct of the clinical study data review and capture. Verifies site compliance...Contract workInterim roleLocal areaImmediate startRemote workFlexible hours
- ...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...
$90k - $130k
..., OK, TN, TX, WA Vanguard Clinical, Inc. is a Contract Research Organization (CRO) headquartered... ..., Data Management and Study Startup. As a small... ...opportunity to successfully lead clinical programs for pharmaceutical... .... The Clinical Research Associate (CRA) will execute...Permanent employmentFull timeContract workInterim roleWork at officeRemote workFlexible hours- ...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...
- ...CEDARS-SINAI is seeking a Clinical Research Associate I to assist in the coordination and implementation of noncomplex research studies. You will work under supervision to support data collection and manage regulatory submissions in compliance with local and federal guidelines...Local area
- ...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
- ...Summary The Clinical Research Associate will perform monitoring and site management activities for Phase... ...that has experience with Breast Cancer studies, lives in Canada (BC, Ontario, Quebec)... ...out of scope activities to Lead CRA/Project Manager Proactively suggest...Contract workInterim roleLocal areaImmediate startRemote work
- ...Bayside Solutions is looking for a motivated Clinical Operations professional for a hybrid role based in Redwood City, CA. The successful candidate will manage the execution of clinical studies, ensuring adherence to regulations and quality standards. Responsibilities...Senior
$136k - $192.5k
Exelixis is looking for a Clinical Trials Manager to coordinate and oversee clinical trials. This role involves managing CROs, developing operational strategies, and ensuring adherence to regulatory standards. The ideal candidate has experience in protocol development...Senior$165k - $215k
...A leading biopharmaceutical company is seeking an Associate Director, Clinical Development Neurology to support clinical trial design and execution. This role requires a PhD in a scientific field and 5+ years in the biopharmaceutical industry, preferably with experience...Senior- A clinical research organization seeks a Senior Clinical Program Manager to lead clinical trials and ensure compliance with regulatory guidelines. This role involves managing project timelines and budgets, collaborating across teams, and analyzing data health metrics....Senior
- ...Initial Therapeutics, Inc. is looking for an Associate Director of Clinical Development in California. This role involves leading the design and execution of clinical studies with responsibilities in regulatory compliance and team management. The ideal candidate will have...Senior
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