NewGlobal Clinical Trial Leader - Contract TalentBurst, Inc.Global Clinical Trial Leader - ContractSouth San Francisco, CAVendor & Budget ManagementVendor Oversight: Participate in vendor selection alongside the PETL; oversee outsourced activities to ensure CROs and vendors deliver strictly against contracted scopes of work. Trial Documentation: Drive and finalize cross-functional activities ensuring the quality delivery of vendor specifications, drug supply forecasting, monitoring/communication plans, Trial Master Files (TMF), and CTMS data.
NewClinical Faculty Operations Manager American Career CollegeClinical Faculty Operations ManagerLos Angeles, CAAs an associate for a certified Great Place to Work, you will join a collaborative, student-centric culture valuing academic integrity, mutual respect, student learning, service, responsiveness, innovation, diversity, and stewardship. For more than 40 years American Career College has had the privilege of educating students seeking careers in healthcare—guiding them through their transformational journey from student to caregiver.
Manager/Senior Manager, GMP Quality Assurance - Clinical, QA - Remote Agios PharmaceuticalsManager/Senior Manager, GMP Quality Assurance - Clinical, QA - RemoteSan Diego, CARemote$110,029–$165,044 / yearManager level is expected to be between $131,035 and $196,553 annualized; final salary will be determined based on various factors including, but not limited to, years of relevant experience, job knowledge, skills and proficiency, degree/education, and internal comparators. Manager, GMP QA Clinical will be responsible for supporting and maintaining high quality levels on Agios Drug Substance, Drug Product, packaged Drug Products and finished goods by Contract Manufacturing Organizations (CMOs).
NewHealthcare IT Project Manager JobotHealthcare IT Project ManagerLos Angeles, CA$70–$80 / hourInformation collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. The successful candidate will have a deep understanding of the healthcare industry and will be able to navigate complex IT environments, with a focus on delivering innovative solutions that drive value and improve patient care.
NewBusiness Development Manager - Bioprocessing Ecolab Inc.Business Development Manager - BioprocessingSan Francisco, CA$126,900–$190,200 / yearThe Business Development Sales Representative will work in collaboration with multiple Account Managers to drive new growth opportunities supporting not only the growth of our Bioprocessing segment but also enabling our clients to develop medicines that improve the lives of their patients. With a broad and innovative portfolio of chromatography technologies, global coverage and leading technical support, Ecolab Bioprocessing supports customers spanning research, emerging biotech, large scale biopharma and contract manufacturers.
Senior Manager, GCP & GVP, QA - Remote Agios PharmaceuticalsSenior Manager, GCP & GVP, QA - RemoteSan Diego, CARemote$131,035–$196,553 / yearConduct and/or oversee consultant auditors in the conduct of GCP/GVP audits of clinical trial internal and PV processes, GCP/GVP vendors, clinical investigator sites, clinical study documents and trial master files in accordance with annual audit plans. The current base salary range for this position is expected to be between $131,035 and $196,553 annualized; final salary will be determined based on various factors including, but not limited to, years of relevant experience, job knowledge, skills and proficiency, degree/education, and internal comparators.
NewHealthcare IT Training Specialist JobotHealthcare IT Training SpecialistLos Angeles, CA$89,000–$100,000 / yearThis role will oversee the IS PMO's most complex projects, which will likely involve a diverse set of components, including healthcare processes, clinical applications & interfaces, business / administrative applications & interfaces, enabling / supporting technology and infrastructure (e.g., hardware, devices, telecom, storage solutions). Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal.
Sr Manager of Quality & Regulatory Michael Page USASr Manager of Quality & RegulatoryWest Hollywood, CA$120,000–$145,000 / yearFull timeOversee product testing processes, including sample coordination, protocols, vendor quotes, and method validation to ensure accuracy, reliability, and regulatory compliance of testing procedures. We are seeking a highly detail-oriented QA & Regulatory Sr Manager to oversee product compliance, safety, and quality systems across the full product lifecycle.
State and Local Government Sales Representative Medline IndustriesState and Local Government Sales RepresentativeWork From Home, CAFull timeBachelor’s degree and at least 2 years of quota-based sales experience demonstrating a background in cold calling, commissioned, full-cycle sales experience OR at least 5 years of quota-based sales experience demonstrating a background in cold calling, commissioned, full-cycle sales experience. Develop and maintain specific account knowledge within assigned territory such as: key decision makers in each department, department hierarchy, products used and how they are used, company products and competitor’s products, new product process and programs.
NewShape Lives, Shape Your Career: Section Chief in Hematology/Oncology Opportunity Veterans Health AdministrationShape Lives, Shape Your Career: Section Chief in Hematology/Oncology OpportunityFresno, CA$325,000–$365,000 / yearFaculty Appointment with UCSF Fresno: Enjoy opportunities for academic engagement, research, and mentorship through a prestigious faculty appointment with the University of California, San Francisco (UCSF) School of Medicine at the UCSF Fresno campus. Live and work in Fresno, a city known for its affordable living, pleasant climate, and proximity to some of California’s most beautiful natural attractions, including Yosemite, Sequoia, and Kings Canyon National Parks.
Medical Oncologist CommonSpirit HealthMedical OncologistRedding, CAThe cancer program is comprised of medical and radiation oncologists, two infusion rooms, 2 radiation centers, clinical trials, lung cancer screening program, community screenings, oncology symposium, patient assistance fund, tele genetics, home health, hospice, palliative care, 17 bed inpatient unit-with daily multidisciplinary rounds, survivorship program, rapid diagnosis clinic, weekly tumor board, cancer resource center, lab, imaging, support groups, bereavement & grief support. Our comprehensive cancer program includes support from nurse navigators/liaison, social worker, pharmacy liaison for our oral medication program, research coordinator, cancer registrars, case managers, registered dietitians, genetic counselors, hospitalists, hospice team and palliative care team.
Clinical Trial Manager/Sr Clinical Trial Manager ErascaClinical Trial Manager/Sr Clinical Trial ManagerSan Diego, CAThe position requires knowledge of clinical trial processes and prior experience in many aspects of trial execution from study start-up to study close-out, including assisting in the management of clinical vendors/CROs and assisting in the oversight of resources, budgets, contracts, and timelines. Our programs take novel approaches to shutting down one of cancer's most commonly mutated signaling cascades, the RAS/MAPK pathway, which affects approximately 5.5 million lives each year worldwide.
Clinical Trial Manager/Sr Clinical Trial Manager Erasca IncClinical Trial Manager/Sr Clinical Trial ManagerSan Diego, CA$145,000–$190,000 / yearThe position requires knowledge of clinical trial processes and prior experience in many aspects of trial execution from study start-up to study close-out, including assisting in the management of clinical vendors/CROs and assisting in the oversight of resources, budgets, contracts, and timelines. Essential Duties and Responsibilities: Manage global clinical trials (Phase 1-3) in oncology indications, ensuring that studies are carried out in accordance with the clinical development plan, ICH-GCP, and FDA/other regulatory agency requirements.
Clinical Trial Manager Imperative CareClinical Trial ManagerCampbell, CAFull timeImperative Care considers factors such as scope and responsibilities of the position, candidate's work experience, education/training, key skills, and internal equity, as well as location, market and business considerations when extending an offer. Contribute operational expertise to the development of study protocols, clinical study documents, and cross-functional clinical initiatives that support innovative neurovascular medical device programs.
Senior Clinical Trial Manager, Clinical Operations Iambic TherapeuticsSenior Clinical Trial Manager, Clinical OperationsSan Diego, CaliforniaThe Senior CTM is accountable for vendor oversight, risk management, timeline and budget performance, and cross-functional alignment to ensure studies are delivered efficiently and in compliance with global regulatory requirements, ICH-GCP, and company SOPs. In close partnership with Clinical Development, Regulatory, Biometrics, and external CROs, this role drives high-quality, inspection-ready trial execution within a collaborative, growth-stage biotech environment.
Clinical Trial Manager Iovance Biotherapeutics IncClinical Trial ManagerSan Carlos, CA$145,000–$165,000 / yearMental: Clear and conceptual thinking ability; excellent judgment, troubleshooting, problem-solving, analysis, and discretion; ability to handle work-related stress; ability to handle multiple priorities simultaneously; and ability to meet deadlines. Support the overall operational execution of clinical studies on one or more clinical programs from initial study synopsis through final project deliverables (ie, database hard-lock, final TLFs, CSR, etc.).
Clinical Trials Manager (Biotechnology, Oncology) Exelixis IncClinical Trials Manager (Biotechnology, Oncology)Alameda, CA$136,000–$192,500 / yearEDUCATION/EXPERIENCE/KNOWLEDGE & SKILLS: Education/Experience: BA/BA/BSN in biological sciences or related field and a minimum of 7 years of related experience; or, MS/MA/MSN in biological sciences or related field and a minimum of 5 years of related experience; or, PhD/PharmD in biological sciences or related field and zero or more years of related experience; or, Equivalent combination of education and experience. This position is responsible for overseeing the execution of clinical trials, collaborating with cross-functional teams, performing oversight activities of Contract Research Organizations (CROs), and providing operational support to the Study Delivery Lead (SDL).
Clinical Trial Manager, CKD Maze Therapeutics IncClinical Trial Manager, CKDSouth San Francisco, CA$143,000–$175,000 / yearThe company is advancing a pipeline using its Compass platform, which allows it to identify and characterize genetic variants in disease and then link those variants to the biological pathways that drive disease in specific patient groups through a process it refers to as variant functionalization. Maze Therapeutics is a clinical-stage biopharmaceutical company harnessing the power of human genetics to develop novel, small molecule precision medicines for patients living with renal, cardiovascular, and related metabolic diseases, including obesity.
Sr. Clinical Trials Manager - VahatiCor T45 LabsSr. Clinical Trials Manager - VahatiCorSanta Clara, CaliforniaRemoteDemonstrated experience leading study-level clinical operations activities, including study startup, vendor management, enrollment forecasting, study metrics, and cross-functional execution. This role serves as the study-level operational owner, accountable for timelines, budgets, vendor performance, enrollment forecasting, study metrics, risk management, and cross-functional execution.
Clinical Trial Manager Imperative Care IncClinical Trial ManagerCampbell, CA$136,000–$152,000 / yearAs a seasoned Clinical Trials Manager, this role will carry out all tactical aspects of assigned clinical trials from study initiation to monitoring adherence to design protocols, identifying and resolving issues at study sites and with CROs, and facilitating effective clinical programs. Imperative Care considers factors such as scope and responsibilities of the position, candidates work experience, education/training, key skills, and internal equity, as well as location, market and business considerations when extending an offer.
Senior Clinical Trials Manager (Biotech Oncology) Exelixis IncSenior Clinical Trials Manager (Biotech Oncology)Alameda, CA$172,000–$245,000 / yearApproaches problems and solutions with an enterprise mindset, considering broad impact to portfolio, regional, and global functions • Ability to study, analyze, and understand new situations and business problems and identify appropriate solutions • Curious in planning; agile in execution • Operationally excellent and drives others towards excellence • Resilient in the context of a rapidly changing environment • Organized with a systematic approach to prioritization. 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.
Senior Clinical Trial Manager Nurix Therapeutics IncSenior Clinical Trial ManagerBrisbane, CACollaborate with Data Management to ensure correct CRFs content is collected, prepare/implement CRF completion guidelines, and coordinate delivery of data updates, listings and study reports. Responsible for selection of vendors/CROs and provide effective ongoing management and oversight to vendors/CROs to ensure compliance and execution of deliverables within the approved budget, study timeline, and study protocol.
Clinical Trial Manager - San Francisco Heartflow IncClinical Trial Manager - San FranciscoSan Francisco, CA$110,000–$150,000 / yearHeartflow is the first AI-driven non-invasive integrated heart care solution across the CCTA pathway that helps clinicians identify stenoses in the coronary arteries (RoadMapAnalysis), assess coronary blood flow (FFRCT Analysis), and characterize and quantify coronary atherosclerosis (Plaque Analysis). The flagship product-an AI-driven, non-invasive cardiac test supported by the ACC/AHA Chest Pain Guidelines called the Heartflow FFRCT Analysis-provides a color-coded, 3D model of a patient's coronary arteries indicating the impact blockages have on blood flow to the heart.
Clinical Trial Manager CareDx IncClinical Trial ManagerBrisbane, CARemote$124,000–$155,000 / yearSpecific responsibilities include, but are not limited to: Lead the end-to-end execution of CareDx clinical trials, including but limited to site identification, study start-up, study conduct, monitoring and closeout, with full accountability of study timelines, budget and metrics; study submission to IRB/ECs; study document development and review (training documentation, ICF, study specific plans, eCRF Guidelines, lab test requisitions, etc.), plans and managing study-specific meetings (e.g. Provide cross-functional leadership across Clinical Operations, Data Management, Medical Affairs and other functional areas serving as the central point of coordination to ensure clear roles, accountability, and seamless clinical trial execution.
Clinical Trial Manager Ossium HealthClinical Trial ManagerSan Francisco, CaliforniaThis position is ideal for someone who thrives in a hands-on, fast-paced environment—someone eager to collaborate across teams and coordinate with internal partners, CROs, and external vendors to deliver excellence in every aspect of our trials. Review and contribute clinical operations input to key study documents including protocols, investigator brochures, regulatory submissions, clinical study reports, and operational plans developed by CRO partners.
Clinical Trial Manager Ossium Health IncClinical Trial ManagerSan Francisco, CA$145,000–$165,000 / yearThis position is ideal for someone who thrives in a hands-on, fast-paced environment-someone eager to collaborate across teams and coordinate with internal partners, CROs, and external vendors to deliver excellence in every aspect of our trials. Review and contribute clinical operations input to key study documents including protocols, investigator brochures, regulatory submissions, clinical study reports, and operational plans developed by CRO partners.
NewClinical Trial Manager Thorough GroupClinical Trial ManagerSan Diego, CaliforniaThis individual will play a critical role in study start-up, site activation, enrollment strategy, risk management, and overall trial execution while collaborating closely with cross-functional stakeholders across the organization. As the organization continues to advance its pipeline, they are seeking an experienced and highly motivated Clinical Trial Manager (CTM) to provide operational leadership for ongoing and upcoming clinical studies.
Clinical Trial Manager EvommuneClinical Trial ManagerPalo Alto, CaliforniaThe Clinical Trial Manager will support the Clinical Operations study lead in study execution and partner closely with CROs, vendors, clinical sites, and cross-functional teams to proactively manage timelines, risks, quality, and performance. The successful candidate will bring independent clinical site monitoring experience gained in a CRA role, sponsor-side study management experience, and the ability to independently drive assigned study activities in a fast-paced, resource-conscious biotechnology environment.
Clinical Trial Manager CTM Corcept Therapeutics IncClinical Trial Manager CTMRedwood City, CA$156,600–$184,300 / yearWith advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. Manages, either directly or through supervised delegation, other study-wide activities such as external vendors, sample handling, drug re-supply, investigator payments, overall data quality, and overall central records quality.
Senior Clinical Trial Manager Sr CTM Corcept Therapeutics IncSenior Clinical Trial Manager Sr CTMRedwood City, CA$170,500–$200,700 / yearThis leader will work with cross-functional teams as well as vendors, clinical sites, and CROs to execute protocol requirements to ensure study deliverables, milestones, and objectives are met within timelines and budget. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today.
Clinical Trial Manager Braveheart BioClinical Trial ManagerSan Francisco, CaliforniaPerform accompanied visits (PSSVs, SIVs, RMVs) with CRO CRAs to ensure study procedure conduct is in accordance with SOPs and protocol procedures and review routine regulatory documents/files in compliance with protocol, regulatory requirements, SOPs, and Monitoring Plan, as required. Our lead product candidate, BHB-1893, is a next-generation oral small-molecule cardiac myosin inhibitor (CMI) being developed for the treatment of obstructive HCM (oHCM) and non-obstructive HCM (nHCM).
Sr. Clinical Trial Manager Structure Therapeutics IncSr. Clinical Trial ManagerSouth San Francisco, CA$171,000–$218,000 / yearManages study sites and study-related activities, including but not limited to: • Site feasibility selection • Start-up • Subject recruitment • Enrollment • Study management • Monitoring • Report review • Site management • Trial master files • Data review • Clean-up • Coordinates with Lead and Finance to track the financial status against budget. • In collaboration with internal stakeholders, responsible for helping to drive the RFP and RFI process, analyze service providers budgets and proposals, conduct bid defense meetings, award services, negotiate, and execute complex agreements (e.g., CRO study-related collaboration agreements).
Clinical Trial Manager Structure Therapeutics IncClinical Trial ManagerSouth San Francisco, CA$146,000–$185,000 / yearIn collaboration with internal stakeholders, responsible for helping to drive the RFP and RFI process, analyze service providers budgets and proposals, conduct bid defense meetings, award services, negotiate, and execute complex agreements (e.g., CRO study-related collaboration agreements). The companys platform combines the latest advancements in visualization of molecular interactions, computational chemistry, and data integration to design orally available superior small molecule medicines that overcome current limitations of biologic and peptide drugs.
Senior Clinical Trial Manager Braveheart BioSenior Clinical Trial ManagerSan Francisco, CaliforniaContribute to, or own the development of, key study documents (e.g., protocols, ICFs, CRFs, monitoring plans, CSRs); under the guidance of the Senior Director, Clinical Operations (or designee) develop operational documents such as vendor specifications, study plans, SIV materials, Investigator Meeting content, and protocol amendments. Perform visits (PSSVs, SIVs, RMVs) as required to demonstrate appropriate oversight of CRO CRAs and study sites to ensure study procedure conduct is in accordance with the study protocol, SOPs, regulatory requirements, and study plans.
NewClinical Trial Manager Arcturus Therapeutics Holdings IncClinical Trial ManagerSan Diego, CATherapeutic Expertise: Proven operational experience running clinical trials in cardiopulmonary indications, with specific experience in Cystic Fibrosis (CF), or chronic cardiopulmonary and lung diseases highly desired. Study Documentation: Draft, review, and contribute to critical study-related materials, including protocols, Informed Consent Forms (ICFs), Clinical Monitoring Plans, site training materials, and lab/pharmacy manuals.
Clinical Trial Manager Denali Therapeutics IncClinical Trial ManagerSouth San Francisco, CA$139,000–$180,000 / yearApplies clinical trial management expertise to resolve operational issues, manage vendors, and ensure adherence to ICH/GCP guidelines, company SOPs, and applicable regulatory requirements. Denali is founded on the collaboration of leading scientists, industry experts, and investors who share the vision that scientific discovery energetically applied to translational medicine is the key to delivering effective therapies to patients.
Clinical Trial Manager, Oncology, Asia Eikon Therapeutics IncClinical Trial Manager, Oncology, AsiaMillbrae, CA$130,000–$142,500 / yearCollaborate with other Clinical Operations functions (Site Engagement & Monitoring Excellence) to efficiently and effectively deliver study site initiation, training, and monitoring activities to ensure adherence to study protocols, regulatory requirements, and ICH-GCP guidelines. In partnership with Clinical Study Management, provide guidance and daily oversight for the successful in-house management of all aspects of international in-sourced clinical trials, delivering high quality study data, on time and on budget.
Senior Manager, Clinical Trials Kaiser PermanenteSenior Manager, Clinical TrialsLos Angeles, CACoordinates and manages clinical research by: providing guidance across teams and in research proposal preparation and submission for portfolios of various trials as applicable; manages multiple teams in the collection, management, analyses, and interpretation of clinical trials data; orchestrating internal resources needed to provide consultation on implementing clinical trials for staff; driving the development and implementation of policies and procedures for developing research protocols and other processes of clinical trials; reviewing, editing, and ensuring accurate compilation of study documentation sent to regulatory bodies (e.g., IRB) for review and approval prior to implementation; may also be responsible for overseeing and managing clinical trial activities (e.g., informed consent process, lab support and processing, pharmaceutical documentation data, sample processing, adverse event assessment process); and may be involved in overseeing research lab operations(e.g., biological specimen collection, including patient preparation, labeling, handling, preservation or fixation, processing or preparation, and transportation and storage of specimens). + Guides research compliance by: leveraging advanced knowledge of clinical trials while influencing the development and implementation of organizational policies and protocols for clinical trial applications in compliance with all applicable federal, state, and local regulations; resolving escalations of compliance and/or quality issues and providing oversight for corrective action plans; disseminating compliance requirement updates to precipitate necessary updates for compliance-monitoring/audit systems and documentation; monitoring and ensuring adherence to new or updated research protocols, procedures, and guidance to continuously improve the confidentiality, privacy, and security of clinical research data; planning the implementation of research protocols, procedures and guidance to ensure confidentiality, privacy, and security of clinical research data within and across units; and overseeing, advising, and providing strategic direction to investigators and other key stakeholders to ensure compliance with IRB approved protocols and local and federal guidelines.
NewManager, Clinical Trial Managers - CNS - U.S. (Remote) Worldwide Clinical Trials Holdings IncManager, Clinical Trial Managers - CNS - U.S. (Remote)CARemote$112,000–$222,000 / yearThe Manager, Clinical Operations Site Management (Franchise Lead) is responsible for providing on‑time and quality delivery of site management services from assigned Clinical Trial Managers (CTMs) within assigned therapeutic area(s) and program(s). Establish regular communication to include quality metrics (such as site visit report compliance, source data verification metrics, and on‑site metrics) and overall project "health" metrics (such as data query status, adherence to the scope of work, and resource status).
Principal Product Manager, Clinical Trials Intelligence Revolution MedicinesPrincipal Product Manager, Clinical Trials IntelligenceRedwood City, CaliforniaThe company’s RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. 12+ years of experience in Product Management, Clinical Data Product Management, Clinical Informatics, Clinical Operations Technology, Clinical Systems, Digital Health, Life Sciences Data Platforms, or related roles within biotech, pharma, CRO, healthcare technology, or another regulated environment.
Principal Product Manager, Clinical Trials Intelligence Revolution Medicines IncPrincipal Product Manager, Clinical Trials IntelligenceRedwood City, CA$186,000–$233,000 / yearRequired Skills, Experience and Education: 12+ years of experience in Product Management, Clinical Data Product Management, Clinical Informatics, Clinical Operations Technology, Clinical Systems, Digital Health, Life Sciences Data Platforms, or related roles within biotech, pharma, CRO, healthcare technology, or another regulated environment. The company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development.
Senior Manager, Clinical Trials Sonova Holding AGSenior Manager, Clinical TrialsValencia, CA$131,560–$164,450 / yearBuild and lead a high-performing team of data managers and scientists; establish data management capabilities, drive evidence generation to support product registration and clinical claims, and lead the build-out of Global Clinical Trials infrastructure including SOPs, systems, governance, and continuous improvement. Proven ability to build strong relationships with external partners, CROs, and vendors; demonstrated experience managing contracts and clinical finance activities across global studies; strong track record in timeline and budget management for complex, multi-country clinical trials.
NewSenior Clinical Trials Data Coordinator City of HopeSenior Clinical Trials Data CoordinatorCACity of Hope's growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago and Phoenix. Working closely with Clinical Coordinators and other research staff, the Senior CTDC independently interprets research protocols, reviews medical records, resolves discrepancies, and helps maintain compliance with study requirements.
Specialist, Clinical Trials Neurocrine Biosciences IncSpecialist, Clinical TrialsSan Diego, CA$89,800–$123,000 / yearThe company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, endometriosis and uterine fibroids, as well as a robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas. Collaborates with clinical research colleagues within Neurocrine, at Contract Research Organizations (CROs), and at Investigator sites to conduct clinical trials adhering to Good Clinical Practice (GCP) and ensuring accurate data, subject safety and impeccable documentation.
Clinical Trial Management Associate, Oncology EMEA/LATAM Eikon Therapeutics IncClinical Trial Management Associate, Oncology EMEA/LATAMMillbrae, CA$122,000–$133,000 / yearEikon's discovery platform is built on groundbreaking innovations from its founders (Nobel Prize, 2014), culminating in the creation of microscopes which enable real time, molecular-resolution measurements of protein movement in living cells, thereby unlocking otherwise intractable classes of proteins as drug targets. You are looking to grow beyond a CTA role and take on more direct responsibility for study deliverables, bringing with you valuable clinical research experience and a strong passion to contribute meaningfully to drug development through consistent operational excellence.