Clinical Trial Assistant
$90k - $108kSocket
Revolution Medicines is a global, commercial-state oncology company dedicated to discovering, developing and delivering innovative medicines for patients with RAS-addicted cancers. Leveraging its differentiated RAS(ON) tri-complex inhibitor platform, the company is advancing a broad, integrated portfolio of oral RAS(ON) inhibitors designed to directly target the active, cancer-driving state of RAS. Founded on rigorous scientific inquiry and a willingness to challenge long-held assumptions, Revolution Medicines is committed to changing the trajectory of disease for patients with RAS-addicted cancers worldwide. Our people are united by a shared way of working: follow the science, challenge assumptions, act with urgency and hold ourselves to a high standard of rigor—all in service of patients. The Opportunity: This is a unique opportunity for an entry-level Clinical Operations Professional. The Clinical Trial Assistant of Clinical Operations, initially reporting to the Director, Clinical Operations, will be responsible for acting as a central contact for the clinical study teams and assist with the clinical execution and management to support RevMed clinical trials. Specifically, you will be responsible for: Assisting in the development, review, distributing, and archiving of study specific documents and reports (plans, training materials, study guides, manuals etc.). Assisting with updating and maintaining clinical systems and any reporting tools. Set up and maintenance of the trial master files (TMF) if applicable, or work with CRO to audit and resolve discrepancies. Create, maintain, and track information for key study related activities. Assisting in the preparation of meeting materials, scheduling meetings, and developing agendas, taking meeting minutes for internal clinical operation team meetings. Gathering investigator and site information, to support study start-up, maintenance and close out activities. Working with cross functional study teams, and vendors to assist in the coordination of clinical trial activities. Support other clinical operations activities as appropriate. Required Skills, Experience and Education: RN or bachelor’s degree in biological sciences or related health related field required. 1-3-years relevant experience in the pharmaceutical or biotech industry. Thrives in a collaborative team setting and is driven by a desire to deploy innovative approaches and technologies in a high-energy environment. Excellent written and verbal communication and people skills. Demonstrate proficiency in Microsoft Word, Excel, and PowerPoint. Demonstrated ability to multi-task, prioritize options. Travel may be required (~25%). Preferred Skills: Experience in working with cooperative group studies and investigator sponsored trials, preferred. Experience in clinical operations or clinical research. Experience of Global clinical trial operations outside the USA. Knowledge of the APAC region. #LI-DN1 #LI-Hybrid The base pay salary range for this full-time position for candidates working onsite at our headquarters in Redwood City, CA is listed below. The range displayed on each job posting is intended to be the base pay salary range for an individual working onsite in Redwood City and will be adjusted for the local market a candidate is based in. Our base pay salary ranges are determined by role, level, and location. Individual base pay salary is determined by multiple factors, including job-related skills, experience, market dynamics, and relevant education or training. Please note that base pay salary range is one part of the overall total rewards program at RevMed, which includes competitive cash compensation, robust equity awards, strong benefits, and significant learning and development opportunities. Revolution Medicines is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital status, medical condition, and veteran status. Revolution Medicines takes protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone. We will only collect, process and use any personal data that you provide to us in accordance with our CCPA Notice and Privacy Policy. For additional information, please contact View email address on click.appcast.io. $90,000—$108,000 USD #J-18808-Ljbffr
$129.4k - $152.3k
...Clinical Research Associate IIRedwood City, California, United StatesFor more than 25 years, Corcept has been singularly focused on the... ...and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver...SuggestedFull time- ...Clinical Trial AssistantThe Clinical Trial Assistant (CTA) provides operational and administrative support to the Clinical Operations team in the execution of Sagimet's clinical trials. This role requires a highly organized, detail-oriented individual who can manage multiple...SuggestedWork at office
$149k - $170k
...has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation...SuggestedFull timeInterim roleWork at office3 days per week- Position: Clinical Research Associate (CRA) Location: Redwood City, CA Length: 6+ Month Contract Job Description Were seeking a Clinical... ...onsite reviewing study documentation across multiple active trials. Review and evaluate: Chain of custody records Laboratory batch...SuggestedContract workInterim role
- 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...SuggestedContract workInterim role
- Corcept Therapeutics is seeking a Clinical Research Associate II to monitor clinical study activities according to Good Clinical Practices... ...setting. Skills in communication, organization, and clinical trial processes are essential. #J-18808-Ljbffr Corcept Therapeutics
- Digital Prospectors in Redwood City, CA is seeking a Clinical Research Associate (CRA) with hands-on monitoring to support multiple ongoing clinical studies. This role focuses on on-site monitoring and ensuring adherence to study protocols, GCP, and regulatory requirements...Interim role
$129.4k - $152.3k
Corcept Therapeutics in Redwood City, California is hiring a Clinical Research Associate II to monitor clinical study activities and ensure... ...will supervise study preparation, coordinate clinical trial components, and liaise with vendors and team members. Applicants...- ScholarshipsAds Inc. is seeking an experienced Clinical Research Associate (CRA) to support a growing clinical team in California. The position is monitoring-focused, with an emphasis on site visits and centralized monitoring across multiple studies. Location: Redwood...Contract work
$25 per hour
...hazardous waste consolidation routines via specified processes as needed Supporting lab equipment maintenance routines as directed Assisting with the ordering and stock integrity of lab supplies through inventory management, procurement, and receiving processes and...Hourly payLocal areaMonday to FridayShift workWeekend workAfternoon shift$135k - $150k
Position: Senior Clinical Research Associate Location: Newark,... ...responsible for the execution of key clinical trial activities as delegated by the Clinical... ...plan; review site audit reports) •May assist with development and coordination of any...Contract workInterim roleLocal areaWorldwide- ...conducted among the VA Hospitals and is seeking a full-time Clinical Research Assistant - Health Educator. The Research Assistant - Health Educator... ...and regulatory audits.Ensure appropriate registration of trial information on clinicaltrials.gov and maintain renewals and...Full timeTemporary workPart timeWork at office
- ...Psychiatry & Behavioral Sciences is seeking a Clinical Research Coordinator Associate to perform... ...years of related experience in clinical trials PHYSICAL REQUIREMENTS Frequently stand,... ...participants according to protocol. Assist in developing recruitment strategies. Coordinate...Fixed term contractWork experience placementWork at officeNight shiftAfternoon shift
$28.72 - $53.61 per hour
...of Dermatology is seeking an experienced Clinical Research Coordinator Associate (CRCA) to... ...investigative work in support of clinical trials, clinical research, or biomedical research... ...participants according to protocol. Assist in developing recruitment strategies. Coordinate...Hourly payFull timeTemporary workPart timeFixed term contractWork experience placementWork at officeFlexible hoursAfternoon shift3 days per week$100k - $120k
...including Reproductive Science Center of the Bay Area—we combine clinical expertise, scientific innovation, and compassionate care. The... ...dental, and vision insurance401(k) with company matchTuition assistance and professional development supportPerformance-based bonus...Work at officeImmediate startMonday to Friday$80k - $100k
About Antheia: Antheia istheadvadvanced biosynthesiscompany transformingpharmaceutical manufacturing and innovation for the 21st century. Antheia's commercially proven technology platform produces high-value pharmaceutical ingredients in a fraction of the time compared...Full timeTemporary workPart timeLocal area$95k - $115k
...range of activities enabling our technical in vivo research and clinical development. About you: You are curious and driven. You want to... ...gavage administration, and necropsy in rodent models. Train to assist and/or perform sterile survival surgical procedures (...Weekend work- ...animal health checks, room temperature/humidity readings, cleaning/husbandry, and facility maintenance. Observe, document, and report clinical signs or adverse events. Measurements Perform tumor volume measurements by caliper and body weight measurements. Record...RelocationShift work
$790 per week
Join a paid research panel and pick the studies you actually want. Focus Group Panel connects everyday people with paid remote focus groups, surveys, and product tests — you choose which ones to join. Active members earn up to $790 a week on the studies they qualify ...Full timePart timeRemote work- Retro Biosciences is seeking a new member of the HSC team to execute tissue and sample processing, focusing on isolating immune cells from animal tissues and coordinating with in vivo studies. You will be reliable and collaborative, supporting time-sensitive workflows and...
$102.93k
...and analyze the results under the guidance of Senior Scientists Assist Senior Scientists in assay development Keep accurate and... ...continue to push the boundaries of molecular diagnostics. Recent clinical outcomes data for Unity Fetal Risk Screen and advances in cancer...Work at office$790 per week
...earn up to $790 a week for your honest opinion. Maxion Research connects everyday people with remote studies, surveys, and product trials run by real companies. Active members earn up to $790 a week on the studies they qualify for. No experience, no selling, no fees....Remote work- Reference: 630651Posted: 2026-09-04Location: Redwood City, CaliforniaCompany: Planet Pharma GroupContact: ApplicationsEmail: ****@*****.*** Research Associate, Target BiologyThe Opportunity:We are seeking a talented senior research associate with ...
$108.6k - $135.7k
...submission to FDA and other regulatory bodies and who can work effectively in a fast-paced environment to ensure that the highest quality clinical assays are developed and launched for our patients.Primary Responsibilities:Design, develop, and validate automated high-...Immediate startWorldwide$75k - $95k
...changes, and cell culture maintenance for iPSC/iHSC differentiation workflows, including weekend coverage as part of a team rotation. Assist with sample prep and handoff for downstream assays, including flow cytometry. Help store and organize large datasets from readouts...- ...Providing technical support.Train new users on instrument startup, QC procedures, sample acquisition, and best laboratory practices.Assist scientists with experimental design and flow cytometry workflows.Develop and maintain standard operating procedures (SOPs) for...
- Reference: 630582Posted: 2026-09-01Location: Redwood City, CaliforniaCompany: Planet Pharma GroupContact: ApplicationsEmail: ****@*****.*** Research Associate DMPK The Opportunity:Develop LC-MS/MS methods and analyze in vivo and in vitro samples to...Work experience placementFlexible hours
- ...platforms.Support implementation, operation, and continuous improvement of laboratory automation workflows and integrated robotic systems.Assist in assay transfer and scale-up activities, including protocol development, reagent qualification, documentation, and workflow...
- ...technical groups in Development, QA/QC and CMC teams supporting the clinical development of products.The senior research associate (SRA)... ...scientific information both written and oral with minimal assistance.• The candidate must be able to demonstrate strong organizational...Work experience placementImmediate start
$22 per hour
...upon experience. What you'll do ~ Provide daily care, feeding, exercise, and enrichment for Pets In Need's shelter animals. Assists with walking and rotating dogs from kennels throughout the day. May participate in showing dogs and or cats to members of the...Hourly payFull timeWork experience placementFlexible hoursAfternoon shift
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