Clinical Project Manager
Trial Library
Our mission is to improve health equity by expanding access to cancer precision medicine. About Trial Library Trial Library, Inc. is a venture-backed startup founded in 2022 focused on accelerating enrollment and retention to clinical trials with an AI-platform. Trial Library is a mission-driven health technology company dedicated to improving health equity in cancer care by expanding access to precision medicine through clinical trials. We work with community oncology sites, patients, and industry partners to ensure that clinical research is accessible, navigable, and inclusive. As a Clinical Associate Project Manager, you will work closely with the Chief Executive Officer, Chief Product Officer, Director of Operations, Provider Customer Success Manager, and Ally Navigation team to support Study Sponsors on the Trial Library Platform. This is a remote position. You will play a pivotal role in ensuring seamless communication and satisfaction between Trial Library and sponsor study teams (our customers). You will act as the main point of contact and manage relationships with study teams for activated clinical trials on the Trial Library platform. You will build strong relationships with sponsors with a focus on close collaboration with study teams to deliver timely reports and insights regarding Trial Library services. Your Responsibilities Serve as the primary liaison between Trial Library and pharmaceutical study sponsors, maintaining regular communication channels, providing updates, and gathering feedback Ownership of all sponsor study team inquiries and troubleshooting to support study teams when necessary Deliver timely reports and insights regarding Trial Library platform’s services and performance for contracted clinical trials to sponsor study teams Bridge the gap between Trial Library operations, provider customer success, and pharmaceutical sponsor reporting Oversee outgoing clinical trial related materials to study teams regarding Trial Library performance and services Oversee and deliver post-sales sponsor presentations from launch of services for a trial to ongoing performance reporting meetings Communicate Sponsor feedback to internal stakeholders to implement changes to Trial Library software such as updates to inclusion/exclusion criteria or clinical trial site locations Demonstrate rigor in being detail oriented in reporting obligations to study teams Develop standardized pharma reporting procedures and best practices Oversee all written documentation sent regarding performance metrics to study teams Maintain up to date knowledge of Trial Library product offering for study teams Your Qualifications Excellent organizational and time management skills Excellent communication skills, oral and written Detail and process oriented Minimum 5+ years of professional experience in oncology clinical research Interact with internal and external customers with a high degree of professionalism Experience with oncology clinical trials, pharmaceutical sponsor reporting needs, and trial enrollment activities Demonstrate a bias towards action and seek to intervene before issues arise Strong communicator and persistent, able to influence behaviors to help drive the desired outcomes Facilitate an analytical approach and use data to drive actions Agile and willing to adapt quickly in order to achieve desired outcomes Demonstrated ability to exercise autonomy in engagement of sponsors Core Values Ally is our favorite moniker The most inclusive approach is worth the work Celebrate measurable improvements in equity outcomes Fearless advocates for belonging Incentives matter to stakeholders choosing our products Taking initiative is actually giving We are accountable for the experience of patients and providers Empathy and humility are the real dynamic duo Trial Library, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to age, ancestry, color, family or medical care leave, gender identity or expression, genetic information, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran status, race, religion, sex (including pregnancy), sexual orientation, or any other characteristic protected by applicable laws, regulations, and ordinances. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us. Seniority level Mid-Senior level Employment type Full-time Job function Project Management and Information Technology #J-18808-Ljbffr
- ...Vir Biotechnology, Inc. in San Francisco is seeking a temporary Project Manager to support cross-functional project management activities for a clinical-stage asset. Ideal candidates should have a strong background in project management within the biopharmaceutical industry...SuggestedTemporary work
- ...Will Be Doing: Responsible for independently leading the clinical trial study team and managing global clinical trial activities on a pivotal trial or... ...activities such as but not limited to: Developing project management plans, strategy, cost and timelines Identification...SuggestedContract workTemporary workLocal areaFlexible hours
$150k - $165k
...by T‑cell engager programs, led by a potential first‑in‑class clinical asset and complemented by an exciting preclinical portfolio in... ...Operations, Lakefront Biotherapeutics is hiring a Clinical Trial Manager to manage the operational aspects of specific clinical studies...Suggested- The University of California, San Francisco is seeking a Research Assistant/Project Manager to support DoC-IT research projects and collaborate with UCSF Health and external researchers. The role involves coordinating activities, developing timelines, maintaining documentation...Suggested
- ...Clinical Research CoordinatorResponsibilities: Ensure each study patient is fully informed of the study at the time of the consent. Patient... ...on each study protocol in order to stay updated. Manage research staff to achieve maximally, meet all deadlines and ensure...Suggested
- ...internationally recognized global leader in HIV clinical care, research and education and has... ...to assist the Principal Investigators, project directors, and Senior Clinical Research... ..., data/specimen collection, data management, and quality assurance. The incumbent will...Work experience placementWork at officeLocal areaWork from homeWorldwideAfternoon shiftEarly shift
- ...prescreening, screening, and consentMaintain and report up-to-date recruitment metricsServe as the main point of contact for participants in clinical trialsAssist with adverse event documentation and reportingAssist in writing and updating clinical study documents (CRFs, SOPs,...
$140k - $170k
...Clinical Trial ManagerSan Francisco, CA or Remote or HybridBraveheart Bio is a clinical-stage biopharmaceutical company focused on developing... ...rapidly evolving therapeutic area.The RoleThe Clinical Trial Manager (CTM) is a key member of the Clinical Operations team and will...Interim roleRemote work$34.32 - $55.19 per hour
...Job Summary The Clinical Research Coordinator will independently execute, manage, and coordinate research protocols, as directed by the Clinical Research Supervisor... .... Ability to work well independently, complete projects timely, and prioritize multiple projects to ensure...Hourly payFull timeWork experience placementWorldwideMonday to FridayShift workDay shift- ...Clinical Trial ManagerBrisbane, CACareDx, Inc. is a leading precision medicine solutions... ...ensure delivery on time. The Clinical Trial Manager (CTM) is responsible for the management... ...trial execution.Prepare and present project debriefings to Clinical Operations management...Full timeWork at officeRemote workWorldwide
$35 - $40 per hour
...experience — talk with your recruiter to learn more. Base pay range $35.00/hr - $40.00/hr Recruiting Manager/ Lead Engineering Recruiter at Amerit Consulting Position: Clinical Research Coordinator Duration: 5-6 Months + Strong Possibility of Extension Pay Rate: $35/hr - $4...Contract work- ...and timings for further discussion.Job DescriptionThe Senior Clinical Trial Manager will independently manage all components of a clinical... ...management. Manage the clinical study budget, ensuring the project remains within scope and that out of scope activities are identified...Work at officeImmediate start
- ...analytical studies on a variety of policies, projects, programs and issues in support of a... ...planning, development, administration, management and implementation; interprets, monitors... ...Study, a randomized, placebo-controlled clinical trial examining the relationship between...Full time
- ...related to the support and coordination of clinical studies of participants with language... ...Ability to work well independently, complete projects in a timely manner, and prioritize... ...substances, database building/analysis, and data management within some of the following: Access,...Full timeWork experience placementWorldwide
- ...limited appointment. We are looking for a Clinical Research Coordinator who is passionate... ...a familiarity with chronic disease management and clinical trials. This position will... ...research protocols, as directed by the Project Manager, Project Coordinator, and/or Principal...Full timeWork experience placementWorldwide
- Lakefront Biotherapeutics in San Francisco is seeking a Clinical Trial Manager to oversee the operational aspects of specific clinical studies from study start‑up through clinical study report, ensuring timelines, budgets, quality of deliverables, and regulatory compliance...
- ...Under the supervision of the Clinical Research Supervisor, Clinical Research Coordinators (CRC) support the management of investigator-sponsored research studies as assigned... ...collection and subject source records, develops project management documents and electronic data...Full timeWork experience placementWork at officeWorldwide
- ...JOB SUMMARY The Clinical Research Coordinator (CRC) will provide research coordination... ...coordination, data/specimen collection, data management, and quality assurance. The incumbent... ...with central data teams for sponsored projects as needed. Maintain data collection forms...Full timeWork experience placementWork at officeLocal areaWork from homeWorldwideWeekend workAfternoon shiftEarly shift
- ...brain tumors). The Neuro-Oncology Service Clinical Trials Program includes pharmaceutical... ...Coordinator Supervisor and Research RN Manager, the Clinical Research Coordinator collects... ...responsibilities, and manage multiple projects simultaneously. Strong interpersonal,...Full timeWork experience placementWork at officeLocal areaWorldwide
- ...The Clinical Research Coordinator will perform independently or with general direction at... ...journey level of the series to execute, manage, and coordinate research protocols, as directed... ...will work closely with Dr. Martinez and project collaborators and partners, to help...Full timeWork experience placementWorldwide
- Job Description The Clinical Research Coordinator will perform independently or with general... ...journey level of the series to execute, manage, and coordinate research protocols, as directed... ...for quality assurance, participate in project team meetings, evaluate eligibility...Work experience placementLocal area
- The Clinical Research Coordinator (CRC) is responsible for independently managing and coordinating clinical research studies within the UCSF Fein Memory and Aging Center.... ...coordination of clinical studies for the UC Multitudes Project. Additionally, the CRC may receive training...Full timeShift work
$120k - $150k
Revolution Medicines is a late-stage clinical oncology company developing novel targeted... ...Professional who has technical expertise in managing Phase I-III clinical trials in an... ...tracking of study participant enrollment projections vs. actuals and study budgets. Serving...Full timeContract workFor contractorsInterim roleLocal area- University of Wisconsin-Madison is seeking a Clinical Research Coordinator II for the Department of Pediatrics to coordinate studies... ...participant recruitment, data coordination, study operations management, and communication across teams, with a focus on delivering rigorous...
$50k
...Medicine, offers a unique opportunity for a Clinical Research Coordinator. This position... ...day operations of the REPLENISH study, a project investigating how aerobic fitness and obstructive... ...and maximal exercise testing while managing all study related data. The coordinator...Permanent employmentFixed term contractImmediate startRemote work$34.32 - $55.19 per hour
Clinical Research Coordinator Psych-Core-Rsch Full Time 83999BR Job Summary Dr. Christina... ...issues, including risk assessment, risk management, malingering, competence restoration and... ...to work well independently, complete projects in a timely manner, and prioritize...Hourly payFull timeWork experience placementWorldwideShift work- ...technology company advancing the diagnosis and management of coronary artery disease, the #1 cause... ...than 500,000 patients worldwide. The Clinical Trial Manager (CTM) is responsible for... ..., vendor management, and completion of project management tasks Develops clinical...Work experience placementWork at officeLocal areaWorldwideRelocationShift work
$73.08k - $93.96k
...analytical studies on a variety of policies, projects, programs and issues in support of a... ...planning, development, administration, management and implementation; interprets, monitors... ...Study, a randomized, placebo-controlled clinical trial examining the relationship between...Full timeShift work- ...that benefit patients worldwide. What you will be doing: The Clinical Trial Assistant is a member of the clinical trial team supporting... ...electronic Trial Master File (eTMF) system and clinical trial management (CTMS). Ensure information is updated during the study per ICH...Work at officeWorldwide3 days per week
$50k
...Category: Academic Staff Employment Type: Regular Job Profile: Clinical Research Coordinator I Job Summary The Department of Medicine... ...aspects of the study. The primary duties of this job involve the management of clinical research trial activity for subjects enrolled in a...Work experience placementWork at office
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