Clinical Research Coordinator (Carlsbad, CA) Profound ResearchClinical Research Coordinator (Carlsbad, CA)Carlsbad, CaliforniaOur Mission: Improving Lives by Providing Advanced Therapeutic Options Our Vision: Creating the Absolute Best Patient-Physician Experience in Clinical Research Our Values: Compassion: We prioritize the patient-physician relationship, ensuring every interaction is service-oriented and patient-centered. You’ll manage study activities from start-up through closeout, lead interactions with study participants, maintain audit-ready documentation, and work directly with investigators, sponsors, and CROs.
Contractor- Clinical Research Coordinator (Oceanside, CA) Profound ResearchContractor- Clinical Research Coordinator (Oceanside, CA)Oceanside, CaliforniaOur Mission: Improving Lives by Providing Advanced Therapeutic Options Our Vision: Creating the Absolute Best Patient-Physician Experience in Clinical Research Our Values: Compassion: We prioritize the patient-physician relationship, ensuring every interaction is service-oriented and patient-centered. You’ll help manage study activities, lead participant visits, complete protocol-required procedures and documentation, and work closely with investigators, sponsors, CROs, and internal teams.
Contractor- Assistant Clinical Research Coordinator (San Diego, CA) Profound Research LLCContractor- Assistant Clinical Research Coordinator (San Diego, CA)San Diego, CAAs an Assistant Clinical Research Coordinator at Profound Research, you'll work alongside experienced clinical research staff at one of our sites, supporting the day-to-day execution of high-volume vaccine clinical trials. High school diploma or technical degree with 3+ years of relevant experience in life sciences, OR Associate's degree with 1+ year of relevant experience, OR Bachelor's degree with relevant coursework or experience in a clinical or life sciences setting.
Sr. Clinical Research Coordinator (Carlsbad, CA) Profound Research LLCSr. Clinical Research Coordinator (Carlsbad, CA)Carlsbad, CALead, implement and coordinate duties for assigned clinical trials including but not limited to study start up, vendor management, subject recruitment, source document review and completion, protocol training, collection of regulatory documents, participant visits, timely data collection and documentation, management and reporting of adverse events, serious adverse events, and deviations, and monitoring visits and follow up. Ensure good documentation practices are applied by all team members when collecting, maintaining, and correcting study data and required records of clinical trial activity including but not limited to source documentation, case report forms, queries, drug dispensation records, and regulatory forms.
Appeals Clinical Specialist MedImpactAppeals Clinical SpecialistSan Diego, CaliforniaThis position focuses on initiating, supporting, and maintaining cost-effective, rational drug, and disease therapy, utilizing distinct but interrelated management and cross-departmental functions for appeal clinical reviews. Must provide adequate support to internal clients; be available for regular interactions and coordination of work with other employees, colleagues, clients, or vendors; as well as be available to facilitate effective decisions through collaboration with stakeholders.
Clinical Research Coordinator II Headlands ResearchClinical Research Coordinator IISan Diego, California$70,000–$75,000 / hourManaging all aspects of a study including participating in the informed consent process, coordinating and performing all visit study procedures per the protocol, entering data and query resolution, Investigational Product management, and managing all study related supplies and equipment, hosting monitoring visits, and attending Investigator Meetings. Under the supervision of the Site Director, the Clinical Research Coordinator II is responsible for the conduct of research protocols, such that the integrity and quality of the clinical research is maintained and the research is conducted in accordance with Good Clinical Practice Guidelines.
Clinical Research Coordinator III Headlands ResearchClinical Research Coordinator IIISan Diego, California$70,304–$75,000 / yearManaging all aspects of a study including participating in the informed consent process, coordinating and performing all visit study procedures per the protocol, entering data and query resolution, Investigational Product management, and managing all study related supplies and equipment, hosting monitoring visits, and attending Investigator Meetings. Type: Regular Full-time Employee Location: Onsite in San Diego, CA (no capabilities for remote or hybrid work) Reports to: Site Director Pay: $70,304-75,000/yr, dependent upon years of experience, licenses and certifications, and education pertinent to the role.
Program Manager - Sourcing Category Management Sharp Health PlanProgram Manager - Sourcing Category ManagementSan Diego, CA$57.74–$74.49 / hourDelivers clinical improvement, cost savings, operational efficiencies, and/or added value by leading cross functional stakeholders through fact/evidence-based, data-driven sourcing initiatives with strong market and competitive analysis, creation of leverage, and professional negotiations to secure the best quality, service, and cost to meet Sharp''s business needs. Work with GPO representatives, as applicable, regarding supplier exceptions to GPO contract language, and collaborate with legal staff to draft the final negotiated contract terms, conditions and exhibits for each contract proposal, securing supplier's authorized signature on the final negotiated contract offers, and meeting with committees to seek contract approval/award.
Senior Clinical Research Associate Crinetics Pharmaceuticals IncSenior Clinical Research AssociateCA$119,000–$149,000 / yearTrain and assist site coordinators, investigators, and CRO (as applicable) in collecting data and executing the study in a timely manner that meets the protocol requirements and timelines/milestones; serve as a resource to site coordinators, investigators and other staff members regarding investigational products and protocols. Conduct site visits including but not limited to qualification visits, initiation visits, interim monitoring visits, and close-out visits; generate clear, comprehensive, and accurate visit reports and letters in a timely manner.
Clinical Research Associate Actalent IncClinical Research AssociateSan Diego, CA$38–$65 / hourAssists the Clinical Team Lead and/or department leads of Clinical Operations in the development and implementation of corrected actions for addressing non-compliance issues at individual sites and across study, including timely follow-up to routine and for cause Quality Assurance audits. Key Responsibilities: • Independently conduct pre-study, initiation, routine monitoring and closeout visits and ensures these visits are completed according to the Clinical Monitoring Plan(s), SOPs, and ICH/GCP.
Clinical Research Coordinator Retina Consultants San DiegoClinical Research CoordinatorPoway, CAResponsible for collecting start-up essential Regulatory documents Signed and filled out 1572 (original and updates) CVs for all investigators (original and updates) Medical licenses for all investigators (original and updates) Financial Disclosure forms from all participating investigators (original and updates) GCP certificates for all participating investigators (original and updates) Signed and dated protocol signature page (original and updates) Signed and dated Investigator Brochure (IB) (original and updates) Collaborates with Principle Investigator (PI), Sub-Investigator (Sub-I), Clinical Research Coordinators (CRCs), Research Assistants (RAs), Medical Assistants (MAs), Ophthalmic Techs, Sponsors, etc.) to conduct and focus on an indication for a specific trial. The Clinical Research Coordinator is responsible for reviewing and understanding research protocols, collecting essential regulatory documents, and managing all aspects of clinical trials at the site level.
Senior Clinical Scientist, Immunology Merck & Co IncSenior Clinical Scientist, ImmunologySan Diego, CA$117,000–$184,200 / yearThe Senior Clinical Scientist applies expertise in disease biology, clinical research, and drug development to support study design, clinical data review, interpretation of results, and generation of scientific insights that inform development decisions and advance protocol objectives. This role partners with Clinical Directors, Study Managers, Clinical Operations, Medical Monitoring, Data Management, Statistics, and Regulatory colleagues to ensure the scientific integrity, quality.
Manager / Sr. Manager, Clinical Operations - FSP West Region Thermo Fisher ScientificManager / Sr. Manager, Clinical Operations - FSP West RegionCarlsbad, CaliforniaRemoteAt least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy. As a Manager, Clinical Operations in FSP, you will oversee, train, resource, coach and performance manage a team, which may be inclusive of various clinical operations focused staff.
Sr Clinical Research Coord Non-RN - Hematology Oncology Research Resources Rady Children's HospitalSr Clinical Research Coord Non-RN - Hematology Oncology Research ResourcesSan Diego, CA$37.63–$51.75 / hourIn addition to having mastered the competencies of the intermediate CRC, the senior CRC demonstrates advanced skills and knowledge along with the ability to support, guide, train, demonstrate or lead study team members in the implementation or study related activities. The senior CRC contributes to the development of new processes, procedures, tools, and training to enhance clinical research activities across the competency domains and conducts quality assurance / quality control checks of the work of others.
Clinical Trial Assistant IQVIA Holdings IncClinical Trial AssistantCarlsbad, CA$35,800–$123,000 / yearAssist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time).
NewClinical Research Associate (CRA) Armata Pharmaceuticals IncClinical Research Associate (CRA)San Diego, CA$86,200–$113,000 / yearThe Clinical Research Associate independently manages assigned investigative sites and is responsible for monitoring clinical trials to ensure subject safety, data quality, protocol compliance, and adherence to applicable regulatory requirements. Armata is a clinical-stage biotechnology company focused on the development of pathogen-specific bacteriophage therapeutics for the treatment of antibiotic-resistant and difficult-to-treat bacterial infections using its proprietary bacteriophage-based technology.
Sr. Clinical Trial Manager Artiva Biotherapeutics IncSr. Clinical Trial ManagerSan Diego, CA$165,000–$185,000 / yearCoordinate and be responsible for the design of study materials such as CRFs, patient diaries, study participation cards and source documents Assist with protocol development, Investigator Brochure (IB) update, and study report completion Manage monitoring activities via contractors or via CRO, (may occasionally include on-site clinical monitoring or co-monitoring with a CRA) at clinical study sites to assure adherence to Good Clinical Practices (GCPs), SOPs and study protocols Provide guidance, direction, and management to CRAs directly or via CRO. Degree in the life sciences preferred At least seven years of experience in clinical trial management Experience in Cell Therapy, Autoimmune or Rare Disease is strongly preferred Past management of people in a matrixed environment Management of global clinical trials Demonstrated working knowledge of GCP, ICH guidelines and FDA regulations Demonstrated ability to work independently and in a team environment Travel of approximately 25% of travel required, with occasional international travel.
NewClinical Research Coordinator (CRC/Phlebotomy experience) Truvian SciencesClinical Research Coordinator (CRC/Phlebotomy experience)San Diego, CAFull timeWHAT YOU WILL BRING: Minimum 3 years of experience working as a Clinical Research Coordinator (or equivalent clinical research role) at a clinical research site or medical device/biotech sponsor, including direct experience conducting participant informed consent and site-level study coordination. Broadly, this role is responsible for site-level clinical operations, regulatory documentation, and coordination of ongoing internal and external clinical studies—including phlebotomy support—to support delivering Truvian’s diagnostic products into diverse, global end markets.
Senior Clinical Research Associate - Oncology Systimmune IncSenior Clinical Research Associate - OncologySan Diego, CA$90,000–$140,000 / yearPrepare the study reference manual, including liaising with the Contract Research Organization (CRO) team (i.e., central lab, specialty labs and vendors) to ensure efficient preparation and delivery of study materials to investigator sites. CRA is responsible for the management and oversight of their assigned clinical study sites to ensure data quality and patient safety in accordance with ICH-GCP guidelines, local regulations, and applicable SOPs.
Staff Program Manager, Clinical Sequencing CDx Thermo Fisher Scientific IncStaff Program Manager, Clinical Sequencing CDxCarlsbad, CA$113,500–$151,300 / yearDemonstrated experience managing strategic biopharma, biotechnology, customer, clinical, CRO, or technology-partner relationships, including expectation-setting, commitment negotiation, escalation management, and resolution of competing priorities across internal teams, clinical sites, laboratories, consultants, and vendors. Working knowledge of regulated product development sufficient to plan and govern execution, including 21 CFR Part 820 design controls, ISO 13485 principles, clinical/analytical validation, risk management, traceability, and quality systems.