Clinical Trials Manager
$146.54k - $189.64kKite Pharma
We’re here for one reason and one reason only – to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We’ve made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet. Join Kite, as we make even bigger advances in cancer therapies, and help shape where our business and medical science goes next. We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Kite and help create more tomorrows. Job Description As a Clinical Trials Manager at Gilead/Kite, you will be responsible for: Coordinating and supervising all aspects of a clinical study. Monitors clinical trial sites. Assists Clinical Program Manager in overall study management. Drafts and coordinates review of relevant documents including protocols, informed consents, case report forms, monitoring plans, investigator brochures, and clinical study reports. Maintains study timelines. Contributes to development of study budget. Contributes to development of RFPs and participate in selection of CROs/vendors. Manage CROs/vendors. Coordinates review of data listings and preparation of interim/final clinical study reports. May contribute to development of abstracts, presentations, and manuscripts, Ensures effectiveness of site budget/contract process. May be asked to train CROs, vendors, investigators, and study coordinators on study requirements. Assists in determining the activities to support a project’s priorities within functional area. Under supervision, may design scientific communications within the company. Excellent teamwork, communication, decision-making and organizational skills are required. Thorough knowledge and understanding of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials is desirable. Must be able to generally understand, interpret, and explain protocol requirements to others. Must be able to prioritize multiple tasks. May serve as a resource for others within the company for clinical trials management expertise. Under general supervision, is able to examine functional issues from an organizational perspective. Must be able to participate in multiple departmental or interdepartmental strategic initiatives under limited supervision. Must have a general, functional expertise to support SOP development and implementation. Travel is required. Basic Qualifications: BS or BA in a relevant scientific discipline and 6 + years of relevant experience OR RN license (2 or 3 year certificate) and 6 + years of relevant experience. Preferred Qualifications: Experience in the following therapy areas is helpful: Hematology, Oncology, Rheumatology, Autoimmune disorders, Familiarity and experience with In-Vivo studies. People Leader Accountabilities: •Create Inclusion - knowing the business value of diverse teams, modeling inclusion, and embedding the value of diversity in the way they manage their teams. •Develop Talent - understand the skills, experience, aspirations and potential of their employees and coach them on current performance and future potential. They ensure employees are receiving the feedback and insight needed to grow, develop and realize their purpose. •Empower Teams - connect the team to the organization by aligning goals, purpose, and organizational objectives, and holding them to account. They provide the support needed to remove barriers and connect their team to the broader ecosystem. The salary range for this position is: Bay Area: $146,540.00 - $189,640.00. Other US Locations: $133,195.00 - $172,370.00. Kite considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*. For additional benefits information, visit: * Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans. Kite is a biopharmaceutical company engaged in the development of innovative cancer immunotherapies with a goal of providing rapid, long-term durable response and eliminating the burden of chronic care. The company is focused on chimeric antigen receptor (CAR) and T cell receptor (TCR) engineered cell therapies designed to empower the immune system's ability to recognize and kill tumors. Kite is based in Santa Monica, CA. For more information on Kite, please visit Sign up to follow @KitePharma on Twitter at For jobs in the United States: Kite Pharma is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, sex, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact View email address on click.appcast.io for assistance. For more information about equal employment opportunity protections, please view the 'Know Your Rights' poster. NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT Kite Pharma will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, (c) consistent with the legal duty to furnish information; or (d) otherwise protected by law. Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team. Kite Pharma provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion. For Current Kite Pharma Employees and Contractors: Please apply via the Internal Career Opportunities portal in Workday. Change The World With Us Everyone at Kite is grounded by one common goal – curing cancer. Every day, we aim to establish a direct line between that purpose and our day-to-day work. We are creating Kite together, with the recognition that the best teams are built by the best people. We maintain an attitude of curiosity, and creativity with each challenge as we develop a new market for cancer therapies. We appreciate and respect one another, and most importantly, we don’t take success for granted. While we’ve come a long way to make what others viewed as impossible, possible, we know one thing is certain. Today is just the beginning.
$36.37 - $58.52 per hour
Direct Jobs is seeking a Clinical Research Coordinator in Santa Monica, California. This role involves supporting the operation of clinical... ..., conduct, and closeout. The Coordinator is responsible for managing research activities to meet deadlines and regulatory compliance...SuggestedHourly pay$140k - $170k
Puma Biotechnology, Inc. is seeking a Senior Clinical Trial Manager in Los Angeles, California. This role involves overseeing all clinical aspects of trials, ensuring compliance with GCP guidelines, and managing study timelines. The ideal candidate will have at least 6...SuggestedRemote jobFull time$36.37 - $58.52 per hour
UCLA Health is looking for a Clinical Research Coordinator based in Santa Monica, CA. The successful candidate will manage clinical research activities throughout the study lifecycle, ensuring compliance with regulations. Key qualifications include a Bachelor's degree and...SuggestedHourly payFlexible hours- UCLA Health is seeking a Senior Clinical Research Coordinator in Santa Monica, CA. This role entails managing clinical research activities, including multicenter trials. Candidates should have strong analytical skills, proficiency with Microsoft Excel, and over 4 years...SuggestedFlexible hours
- The University of California - Los Angeles Health is seeking a Clinical Research Coordinator to support operational management of clinical research. This role involves managing study activities, ensuring compliance with regulations, and collaborating with Principal Investigators...Suggested
$89.45k - $143.9k
Direct Jobs is seeking a Senior Clinical Research Coordinator in Santa Monica, California. This role involves overseeing clinical trials from start to finish while ensuring compliance with protocols and regulations. Candidates must have a minimum of 4 years in a clinical...$27 - $33 per hour
...accommodation or an alternative application process. Clinical Research Coordinator FullTime Technical Alliance Clinical... ...Coordinator (CRC) supports the conduct of clinical trials by coordinating study visits, managing data collection, and ensuring compliance with...Hourly payFull timeH1bMonday to Friday- ...Position: Clinical Research Coordinator Location: West Hollywood, CA 90046 Overview The Clinical... ...CRC is responsible for ensuring clinical trials are conducted in compliance with study... ...detail, and the ability to effectively manage multiple clinical research activities while...Contract workWork at officeLocal area
- ...RDI is a trial management organization connecting IVD manufacturers and pharmaceutical companies with a network of doctors participating in... ...provide sample procurement, conduct testing, and simplify the clinical trial process for our clients while recruiting, educating,...
$50 - $67 per hour
...Clinical Research Coordinator A dynamic and experienced Consulting Clinical Research Coordinator... ...drive the success of diverse clinical trials including Phase I‑IV industry, NIH, and... ...capacity, with demonstrated success in managing complex clinical trials. Extensive...Hourly payFlexible hours$36.37 - $58.52 per hour
...Description The Department of Psychiatry is seeking to hire a Clinical Research Coordinator to join the TMS Research Service. You will contribute to the overall operational management of clinical research activities from design, set up, conduct, through closeout. Primary...$36.37 - $58.52 per hour
...The Department of Medicine is seeking a Clinical Research Coordinator to support the full... ...research activities for one or more studies, managing day-to-day operations, and prioritizing... ...math ability and knowledge of clinical trials research budgeting process to assist...Hourly payFlexible hours$38 - $40 per hour
...Clinical Research Coordinator - Spanish Bilingual Compensation: ~ ($38–$40/hr) Project We are seeking a high-level Spanish speaking... ...study lifecycle—from site activation and patient enrollment to IP management and data close-out. Strict Requirements Clinical Skills:...Private practiceLocal areaRemote workRelocation$25 - $40 per hour
...Part-time employment to start. This position is to fulfill a role for Clinical Research Coordinator at multiple sites (Oxnard, Palmdale, Valencia, Sherman Oaks, West Hills, Downtown LA, Inglewood). Some days you will work remote. Past experience as a Clinical Research...Hourly payPart timeLive inRemote work$43 - $53 per hour
...site network, fully dedicated to oncology clinical research. Throughout our history, START... ...“Hope Through Access” to cutting edge trials throughout the United States and Europe.... ...will be involved in patient treatment and management. Maintain an up‑to‑date contact list....Currently hiringWork at officeLocal areaWorldwideMonday to FridayFlexible hours$36.37 - $58.52 per hour
..., and EEG operations (preferred) Analytical skills to evaluate clinical research protocols and regulatory requirements, identify issues... ...and data entry systems Strong organizational skills with the ability to manage multiple projects and competing deadlines UCLA HealthHourly payRemote workMonday to Friday$62.4k - $83.2k
...Clinical Research Coordinator Inglewood Clinical is part of the Irvine Clinical Research... ...s Disease prevention and treatment drug trials, and our doctors were the largest... ...operational excellence. Job Duties Study Management: Serve as the primary or co-coordinator...Hourly payFull time- ...potential patients for protocol eligibility, presenting non-medical trial concepts and details to patients, and participating in the... ...Institutional Review Board. Maintains research practices using Good Clinical Practice (GCP) guidelines. Maintains strict patient...Local area
- ...year of employment Job Description The Clinical Research Coordinator will work under the... ...Investigator, Sub-Investigators, and/or Director/Manager of Clinical Research Operations to... ...applicable federal regulations for clinical trial participation. Strong Communication...Local areaFlexible hours
$24 - $39.76 per hour
A leading medical center in Los Angeles seeks a Clinical Research Coordinator I to manage patient scheduling, document research activities, and comply with federal regulations. Ideal candidates have a high school diploma or GED, with a preference for a bachelor's degree...Hourly payFull time- A leading medical center in Los Angeles is seeking a Clinical Research Coordinator II to manage study coordination, including patient scheduling and data collection. The role requires effective communication with medical personnel and compliance with FDA regulations. Candidates...
- Cedars-Sinai in Los Angeles is seeking a Clinical Research Coordinator to support clinical research protocols effectively. This role involves processing laboratory specimens, maintaining records, and facilitating patient recruitment. The ideal candidate holds a High School...Remote work
- UCLA Health is seeking a Clinical Research Coordinator to join a centralized clinical research team focusing on pediatric trials. This role encompasses various activities including recruitment, data management, and adherence to clinical research standards. The ideal candidate...Flexible hours
- Cedars-Sinai is looking for a Clinical Research Coordinator I in Los Angeles to oversee clinical studies, ensuring compliance with federal regulations while coordinating with patients and medical personnel. The ideal candidate should hold at least a High School Diploma...
- The University of California - Los Angeles Health is seeking a Clinical Research Coordinator to manage clinical research studies from design to closeout. This role requires strong communication and organizational skills, along with the ability to comply with regulations...
- Men's Health Foundation in West Hollywood is seeking a Clinical Research Coordinator to participate in clinical research projects. The role involves ensuring compliance with regulations and maintaining high professional standards in research operations. The ideal candidate...
- Direct Jobs is seeking a Clinical Research Coordinator I in Los Angeles, CA. The role involves independently managing clinical research studies, ensuring compliance with federal regulations, and maintaining patient confidentiality. Responsibilities include coordinating...
- ...the California Heart Center is to integrate quality health care, clinical research, and continuing education to create an environment... ...potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and supporting the...Local areaImmediate start
- A leading medical institution in Los Angeles is seeking a Clinical Research Coordinator to support clinical research protocols. The role includes managing laboratory specimens, scheduling patient appointments, and ensuring compliance with research protocols. Ideal candidates...
- Overview EXPERIENCED Clinical Research Coordinator - Onsite Job Details: 15-20 hours/week for the first 3 months... ...Coordinator (CRC) to join our dynamic clinical trials team. The CRC will plan, coordinate, and manage all activities associated with the initiation, conduct...Full timeWork at officeLocal areaRemote workVisa sponsorship
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