Research Assistant, Medical Affairs San Diego, CA (Hybrid) ESRhealthcare and EXEC STAFF RECRUITERSResearch Assistant, Medical Affairs San Diego, CA (Hybrid)San Diego, CaliforniaThe Research Assistant will play an important role in supporting our account-level data initiative to help healthcare providers evaluate glycemic outcomes, gain insights into patterns of settings and outcomes, and identify optimization opportunities. Provide support for team conference activities, such as booking meeting rooms, coordinating meetings with key opinion leaders, coordinating ad boards, and supporting conference notetaking and report development.
PREVENT Research Assistant (Part-Time; English/Arabic Bilingual Required) San Ysidro Health CenterPREVENT Research Assistant (Part-Time; English/Arabic Bilingual Required)San Diego, CAUnder the supervision of the Program Manager and Program Coordinator the Research Assistant (RA) will be responsible to support and will help support day-to-day functions of the PREVENT Research Program. Almost 50 years later, San Ysidro Health now provides innovative care to over 108,000 patients through a vast and integrated network of 47 program sites across the county.
Prevent Research Assistant (Arabic Or Spanish Bilingual Required) San Ysidro Health CenterPrevent Research Assistant (Arabic Or Spanish Bilingual Required)San Diego, CAEssential Functions of the Job: Edit and submit study protocols and other required research documentationProvide information regarding respiratory pathogen prevention and testingRecruit and enroll study participants according to study protocolsObtain informed consent for all study participantsPerform data entry using the study data management system (e.g., REDCap, Access, EPIC)Performs or assists with routine data verification and quality controls to ensure data integrity and consistencyAssist in the setup, operation, and maintenance of research equipment and/or instrumentation as specifically instructedTrack research participants and perform follow-up tasks according to study protocolFollow study protocols (IRB, SOPs, MOPs), and adheres to study protocols, Good Clinical Practice (GCP), and ethical research principlesProvide assistance in a variety of tasks in support of established recruitment and retention goalsDemonstrate skills and abilities by following the guidelines in venipuncture, heel/finger stick, and/or saliva sample collectionProvide assistance to the Principal Investigator, Program Manager, and Program Supervisor as needed. Technical Knowledge and Skills Required to Perform the Job: Superb organizational ability and exceptionally analyticalAbility to work well in a fast-paced, deadline driven, collaborative environmentProficiency in administrative skills and time managementExperience and knowledge with Microsoft.
NewAoURP Research Assistant (Bilingual English/Spanish Required) San Ysidro Health CenterAoURP Research Assistant (Bilingual English/Spanish Required)San Diego, CAUnder the direct supervision of the All of Us Research Program Supervisor, the Research Assistant will help support day to day functions of the All of Us Research Program with a focus on enrolling pediatric patients and their families. Position Summary: The San Ysidro Health (SYHealth) Research and Health Promotion Department augments the health center's clinical care with health education, health promotion, and research programs for patients and community members.
Clinical Trials Research Assistant - Medicine University of CaliforniaClinical Trials Research Assistant - MedicineSan Diego, CARemoteUC San Diego is a student-centered, research-focused, service-oriented public institution recognized as one of the top fifteen research universities worldwide, and a top ten public university. 15 years later, my work improves operational efficiencies, provides valuable programs to the university, and even helps students bring their innovations to life.
Cardiologist - Clinical Research Investigator ECN Operating LLCCardiologist - Clinical Research InvestigatorSan Diego, CA$150–$250 / hourThe ideal candidate will play a critical role in the conduct of clinical trials by serving as a Principal Investigator (PI) or Sub-Investigator , while continuing to provide high-quality medical care to adult patients within a clinical research setting. Elite Clinical Network (ECN) is seeking a dedicated and research-oriented Cardiologist - Clinical Research Investigator to join our expanding team of clinical professionals.
Clinical Research Coordinator (CRC/Phlebotomy experience) Truvian SciencesClinical Research Coordinator (CRC/Phlebotomy experience)San Diego, CA$60,000–$80,000 / yearWHAT 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. WHAT YOU WILL DO: 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.
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.
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 II Headlands Research IncClinical Research Coordinator IISan Diego, CA$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. Under the supervision of the Site Director, the Senior Clinical Research Coordinator 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 Research IncClinical Research Coordinator IIISan Diego, CA$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. Under the supervision of the Site Director, the Senior Clinical Research Coordinator 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 Manager Headlands Research IncClinical Research ManagerEscondido, CA$100,000–$105,000 / yearLead regular team meetings to discuss status of current projects, plan for future projects, provide updates on new company initiatives, seek feedback regarding team barriers, etc. Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver's license information, etc) via email or messenger tools, or for a financial deposit of any kind.
Clinical Research Associate (CRA) ResMed IncClinical Research Associate (CRA)San Diego, CA$86,000–$128,000 / yearThe Medical Affairs team collaborates with the leaders of Sleep, Respiratory Care, SaaS, ResMed Healthcare, and Asia Growth Markets to ensure our work, especially our clinical research and market access projects, align with their strategic priorities. The two, research and compliance, work hand-in-hand, and when balanced properly allow us to generate important clinical, economic and market evidence, that improves the lives of patients in ways that are scientifically valid, clinically relevant and ethically sound.
Clinical Research Coordinator (CRC/Phlebotomy experience) Truvian Sciences IncClinical Research Coordinator (CRC/Phlebotomy experience)San Diego, CA$60,000–$80,000 / yearWHAT 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. WHAT YOU WILL DO: 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.
NewClinical Research Coordinator (Crc/Phlebotomy Experience) Truvian Sciences IncClinical Research Coordinator (Crc/Phlebotomy Experience)Sorrento, CA$60,000–$80,000 / yearWHAT 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. WHAT YOU WILL DO: 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.
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.
NewClinical Research Associate Orso HealthClinical Research AssociateSan Diego, CA$24–$29 / hourUnder the supervision of the Clinical Research Coordinator and Director of Research Operations, the CRA will assist with subject scheduling, data entry, biospecimen coordination, and regulatory documentation. The Clinical Research Associate will support the operational and administrative functions of clinical trials, serving as a key liaison between study participants and the research team.
Clinical Research Coordinator (San Diego, CA)* Profound Research LLCClinical Research Coordinator (San Diego, CA)*Carlsbad, CAYou'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. Bachelor's degree with 1+ year of relevant experience, OR Associate's degree with 3+ years of relevant experience, OR High school diploma with 4+ years of relevant experience and at least 1 year of CRC experience.
Clinical Research Coordinator Odyssey Systems Consulting Group, Ltd.Clinical Research CoordinatorSan Diego, CaliforniaFull timePosition Summary: Odyssey is looking for a Clinical Research Coordinator to coordinate and assure the integrity of all activities associated with conducting Traumatic Brain Injury Center of Excellence (TBICoE) clinical investigations in TBI, brain health, and related outcomes. Prepares requests for actions/proposals to include assisting with and providing coordination for grant proposal applications and their associated documentations and requirements as Facilitates the flow and approval processes for relevant projects as needed or requested.
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.