IS Project Manager - Clinical Systems Portfolio BayCare Health SystemIS Project Manager - Clinical Systems PortfolioClearwater, FLIn this role, you will lead complex technology initiatives that impact clinical operations across the organization, partnering with stakeholders at all levels to ensure successful project delivery from planning through activation. Our integrated health system includes 16 community-based hospitals, a long-term acute care facility, home health services, outpatient centers, and thousands of physicians.
Project Manager For Clinical Operation AccuScan SciencesProject Manager For Clinical OperationMilpitas, CAThis role plays an important part in keeping teams aligned around shared goals, maintaining momentum across interconnected workstreams, and supporting effective coordination among scientific, operational, regulatory, and quality-focused stakeholders. Our work sits at the intersection of genomics and precision oncology, with a focus on advancing diagnostic capabilities that can help inform patient care and clinical decision-making.
Project Manager I Advocate Health and Hospitals CorporationProject Manager IWake Forest, North CarolinaProviding care under the names Advocate Health Care in Illinois; Atrium Health in the Carolinas, Georgia and Alabama; and Aurora Health Care in Wisconsin, Advocate Health is a national leader in clinical innovation, health outcomes, consumer experience and value-based care. Headquartered in Charlotte, North Carolina, Advocate Health services nearly 6 million patients and is engaged in hundreds of clinical trials and research studies, with Wake Forest University School of Medicine serving as the academic core of the enterprise.
Project Manager For Clinical Operation AccuraGenProject Manager For Clinical OperationMilpitas, CAThis role plays an important part in keeping teams aligned around shared goals, maintaining momentum across interconnected workstreams, and supporting effective coordination among scientific, operational, regulatory, and quality-focused stakeholders. Our work sits at the intersection of genomics and precision oncology, with a focus on advancing diagnostic capabilities that can help inform patient care and clinical decision-making.
Senior Clinical Research Associate - (Multi-Site Coordinator) - Pediatrics Baylor College of MedicineSenior Clinical Research Associate - (Multi-Site Coordinator) - PediatricsHouston, TX$70,618–$83,080 / yearDistributes data summaries to investigators and coordinators at study sites; this may occur periodically throughout study or only at the end of data collection and analysis. Creates and maintains records of IRB submissions, approvals, and expiration dates for all study sites (e.g. in electronic clinical trial management system).
Clinical Research Center Manager Harvard Medical Faculty PhysiciansClinical Research Center ManagerAs needed, provide age specific care to pediatric and adult patients with or without diabetes mellitus in a collaborative practice, by using competencies in history taking, physical examination, assessment and interpretation of laboratory and related diagnostic tools for purposes of screening and safety assessments of participants participating in clinical research studies. As part of its dedication to excellence, Longwood Specialty Physicians is associated with Harvard Medical Faculty Physicians (HMFP) and Beth Israel Deaconess Medical Center (BIDMC), renowned organizations that offer access to innovative research, advanced education, and a network of 680+ physicians.
Clinical Research Nurse (Full Time, Days) Nicklaus Children's HospitalClinical Research Nurse (Full Time, Days)Miami, FLBSN - Bachelors of Science in Nursing • RN Licensure within the State of Florida or Multi-State Enhanced Nursing License Compact (eNLC) - maintain active and in good standing throughout employment • IATA certification completion required within 3 months of hire date • American Heart Association ACLS (Advanced Cardiovascular Life Support) certification required within 2 months of hire • American Heart Association PALS (Pediatric Advanced Life Support) certification completion required within 6 months of hire • American Heart Association BLS - maintain active and in good standing throughout employment • 2-4 years of professional research or healthcare experience • 1-3 years of Phase 1 clinical research experience • ARNP highly preferred • Clinical research certification (e.g., CCRC, CCRP, CRA) preferred • Bilingual in English/Spanish preferred • Pediatric Nursing experience in an acute care setting preferred • Experience in neurology, neurosurgery, or oncology preferred • Experienced with database management tools and/or REDCap preferred • In-depth knowledge of Phase I clinical trials • Demonstrated knowledge of clinical research trial design and execution • Experienced with electronic medical record and clinical trial management software applications • Strong written and verbal communication skills • Excellent interpersonal skills • Excellent problem-solving skills • Effective organizational and project management skills • Ability to pay close attention to detail • Ability to comprehend professional and scientific journals • Ability to apply principles of logical and scientific thinking to a wide variety of intellectual and practical problems • Ability to establish and maintain effective working relationships with coworkers, managers and clients • Proficiency in Microsoft Office including Access, Word, Excel, Outlook, and PowerPoint • Willing to work off-hours depending on the study requirements. This research position reports directly to the NCH-RI Clinical Trials Office (CTO) Manager but works closely with Lead CRAs, Study Team (PI, Sub-Is, CRC, etc.), NCH-RI departments and Nicklaus Childrens Hospital (NCH) department administrators, and other clinical research professionals to help ensure that clinical research and related activities are performed in accordance with all applicable Federal regulations, NCH/NCH-RI applicable policies and sponsor policies/requirements.
NewResearch Project Manager Genomic Medicine University of Texas MD Anderson Cancer CenterResearch Project Manager Genomic MedicineHouston, TXThe position will maintain professional and cooperative relationships with business partners, administrators, research scientists/investigators, and other executive level healthcare and academic professionals to ensure efficient communication, follow-thorough, and coordination of scientific short/long range goals are met. Manage budget tracking, procurement activities, and financial reporting while providing comprehensive logistical support, meeting coordination, communications management, and follow-through on key action items.
Clinical Study Manager Connexion Systems + EngineeringClinical Study ManagerDurham, NCThis position is responsible for coordinating study activities, managing CROs and vendors, overseeing timelines, and ensuring studies are conducted in compliance with ICH/GCP guidelines, regulatory requirements, and established SOPs. We're looking for a proactive clinical operations professional who thrives in a collaborative environment and can successfully manage multiple priorities while maintaining compliance, quality, and study timelines.
Research Project Mgr Baylor Scott & White HealthResearch Project MgrPlano, TXOther duties include negotiating and monitoring project budgets, monitoring regulatory agencies, and assisting in writing proposals, grants, contracts, and budgets. The Research Project Manager leads the team and plans, develops, implements, manages, and reports on a research program.
Experienced Study Start-Up Project Manager (Remote) Medpace, Inc.Experienced Study Start-Up Project Manager (Remote)RemoteResponsibilities: Efficiently manage successful execution of global start-up, maintenance, and close-out studies; Effectively lead others in a matrix environment; Perform quality checks on submission documents and site essential documents; Prepare and approve informed consent forms; Serve as a Sponsor point of contact for start-up and regulatory submissions items; Review pertinent regulations to develop proactive solutions to start-up challenges; Prepare new business proposals and present during bid defenses, general capabilities meetings, and audits; Contribute to the growth and development of departmental staff, processes and systems. When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
NewCredentialed Trainer I - Converge Clinical Informatics CHRISTUS HealthCredentialed Trainer I - Converge Clinical InformaticsAlamogordo, NMThe Credentialed Trainer works with the Principal Trainers, Clinical Informatics Analysts, Clinical Informaticists, Health System leaders and Education to assure end users can use the system. • Provide onsite end user support through rounding, attending associate fairs and other support activities; proactively seek out support needs and provide innovative ideas.
Clinical Research Project Manager - Breast Oncology Dana-Farber Cancer Institute IncClinical Research Project Manager - Breast OncologyBOSTON, MARemote$76,910–$85,295 / yearReporting to faculty, research and/or disease group managers, and/or Clinical Trials Office (CTO) leadership, the Clinical Research Project Manager I identifies project plan variances and develops contingency plans to maintain project milestones. Administrative Support: Schedule research team meetings and conference calls, facilitate mailings, and perform other project-related administrative tasks to ensure effective communication and coordination among team members and external collaborators.
Clinical Trials Fiscal Manager Fred Hutchinson Cancer CenterClinical Trials Fiscal ManagerSeattle, Washington$109,699–$173,347 / yearFull timeResponsibilities: Oversee clinical trial pre-award financial activities including but not limited to preparation of complex clinical trial budgets, study and funding intake submissions, sponsor funding applications, and coordination with the contracts team to draft and execute underlying clinical trial funding agreements. As a key leader in the Cancer Consortium’s central clinical trials office, Clinical Research Support (CRS), the Fiscal Manager is responsible for driving strategic initiatives, fostering collaboration, and ensuring operational success across multiple research programs.
Regional Clinical Study Associate Manager BeOne Medicines AGRegional Clinical Study Associate ManagerCA$96,300–$131,300 / yearManages the regional clinical operations team (incl oversight of external partners working on the regional level) and acts as point of escalation for resolution of issues within the region for the assigned study, or supports the Regional Clinical Study (Sr) Manager with specific aspects of regional study delivery. Manages the regional clinical operations team effectively, ensures effective decision making and acts as point of escalation for resolution of issues within the region for the assigned study or drives specific aspects of regional study delivery in collaboration with the Regional Clinical Study (Sr) Manager.
NewTravel Trauma Clinical Program Coordinator RN - $3,133 per week ARMStaffingTravel Trauma Clinical Program Coordinator RN - $3,133 per weekCharleston, WVWe accomplish this through our total dedication to our clients and field associates, our over 15 years of experience, a strong and diverse poor of medical professionals, and the high level of loyalty of our internal staff. The Lead Trauma Performance Improvement Coordinator is responsible for overseeing the trauma performance improvement program under the guidance of the Trauma Services Program Director and Trauma Medical Director.
Protocol Project Manager UCSF Medical CenterProtocol Project ManagerSan Francisco, CAEnsure timely processing of new protocols through the activation pipeline including Medicare coverage analysis and budget sign off, informed consent approval and IRB submission, contract execution, and billing set up; prepare reports and trackers to keep the Disease Site Committee appraised of activation status for all new protocols. Forward all investigator-initiated modification requests to the protocol editors in a timely manner, and send all protocol amendments from industry sponsors to the regulatory affairs specialists, ITR Clinical Trials Budget Office and post-award analysts.
Senior/Clinical Trial Manager CTM Vor BioPharma IncSenior/Clinical Trial Manager CTMBoston, MA$140,000–$155,000 / yearProvide clinical operations expertise and strategic leadership in the evaluation, selection, and management of CROs and other external vendors to ensure successful clinical trial implementation and execution of Vor Biopharma clinical trials and ensure that performance expectations are met. Provide technical expertise to oversee the development of clinical documents (protocol, informed consent form, CRF, monitoring plans, regulatory submission documents, clinical study report, investigator brochures, etc.
Senior Clinical Trials Manager (Biotech Oncology) Exelixis Inc.Senior Clinical Trials Manager (Biotech Oncology)Alameda, CA$172,000–$245,000 / yearEDUCATION/EXPERIENCE/KNOWLEDGE & SKILLS: Education/Experience: BA/BS in biological sciences or related field and a minimum of 9 years of related experience; or, MA/MS in biological sciences or related field and a minimum of 7 years of related experience; or, PhD/PharmD in biological sciences or related field and a minimum of 2 years of related experience; or, Equivalent combination of education and experience. SUMMARY/JOB PURPOSE: The Senior Clinical Trials Manager, Clinical Operations, combines end-to-end design, execution, and reporting of clinical trials with leadership in study teams and across matrix teams.
Senior Clinical Trials Manager (Biotechnology, Oncology) Exelixis Inc.Senior Clinical Trials Manager (Biotechnology, Oncology)Alameda, CA$172,000–$245,000 / yearEDUCATION/EXPERIENCE/KNOWLEDGE & SKILLS: Education/Experience: BA/BS in biological sciences or related field and a minimum of 9 years of related experience; or, MA/MS in biological sciences or related field and a minimum of 7 years of related experience; or, PhD/PharmD in biological sciences or related field and a minimum of 2 years of related experience; or, Equivalent combination of education and experience. SUMMARY/JOB PURPOSE: The Senior Clinical Trials Manager, Clinical Operations, combines end-to-end design, execution, and reporting of oncology clinical trials with leadership in study teams and across matrix teams.