Clinical Trials Regulatory Specialist 2 (Remote Opportunity) Stanford UniversityClinical Trials Regulatory Specialist 2 (Remote Opportunity)CARemoteYou will engage with company sponsors, clinical research organizations, Stanford investigators and their study teams, the Stanford Institutional Review Board (IRB), other external IRBs, the FDA, and various regulatory authorities, as well as any other entities that contribute to clinical research at our institution. CRH is seeking a mission-driven Clinical Trials Regulatory Specialist 2. In this role, you will collaborate with a high-performing team of clinical operations staff and medical experts.
Senior Human Resources Business Partner The Staffing Resource Group, IncSenior Human Resources Business PartnerLos Angeles, CA$120,000–$145,000 / yearWe provide contract, contract-to-hire, and direct hire placements across a wide range of critical roles including Scientists, Formulators, Engineers, QA/Regulatory Affairs, Microbiologists, Manufacturing Technicians, Supply Chain/Procurement Specialists, Project Managers, and Business Development professionals. This highly visible leadership role partners closely with executive leadership and corporate HR to drive employee engagement, strengthen employee relations, ensure regulatory compliance, and support organizational growth across a multi-site healthcare environment.
OB/GYN Pelvic Pain Specialist - HS Assistant, Associate or Clinical Professor University of California Los AngelesOB/GYN Pelvic Pain Specialist - HS Assistant, Associate or Clinical ProfessorLos Angeles, CA$250,000–$325,000 / yearPublish scholarly work in peer-reviewed journals.\n \nRequired Qualifications:\n\n MD or DO degree or equivalent \n Board certification or board eligibility in Obstetrics and Gynecology\n Active or eligible for medical licensure in California\n Demonstrated clinical interest and experience in chronic pelvic pain and vulvodynia management\n Strong commitment to patient-centered, multidisciplinary care\n Excellent communication and interpersonal skills\n \nPreferred Qualifications:\n\n Experience with trigger point injections, nerve blocks, and botulinum toxin administration\n Training in trauma-informed care approaches\n Familiarity with pelvic floor musculoskeletal examination techniques\n Experience coordinating multidisciplinary pain management teams\n Prior academic appointment or teaching experience\n Research experience in chronic pain conditions\n \nRank and salary will be commensurate with experience, credentials and prior accomplishments.\n \nThe posted UC Salary Scales set the minimum pay determined by rank and step at appointment. The successful candidate will provide comprehensive, evidence-based care for patients with complex pelvic pain conditions while contributing to medical education, research, and quality improvement initiatives.\n \nClinical Responsibilities:\n\n Provide comprehensive evaluation and non-surgical management of patients with chronic pelvic pain, vulvodynia, and related conditions including interstitial cystitis/bladder pain syndrome, irritable bowel syndrome, and pelvic floor dysfunction.\n
Assistant Professor of Bioengineering American Water Resources AssociationAssistant Professor of BioengineeringLos Angeles, CAThe selected candidate will be expected to teach and develop undergraduate and graduate courses within their expertise; perform high-quality research in their specialized area and present findings from their research in peer-reviewed publications and conferences; establish a strong research program supported by extramural funding; be involved in service to the university and broader scientific community; and collaborate with faculty in diverse disciplines. Also, in our candidate pools, we seek to attract greater representation of women, scholars of color, people with disabilities, veterans, and others who have historically been underrepresented in bioengineering; attract students from a wide range of countries and backgrounds; accelerate progress in building a faculty and staff varied in background and thought; and maintain an environment that fosters interaction and understanding within our community.
Medical Assistant 3 UCSF Medical CenterMedical Assistant 3California, CAUCSF Transgender Care's mission is to provide high quality, evidence-driven, patient-centered gender affirming medical and surgical care to all transgender, gender non-binary, and gender non-conforming people, to conduct cutting edge research on transgender medical and surgical care, guided by community participation, and to teach our key principles of evidence-based, community-informed transgender care and research to the next generation of medical providers. Uses effective communication skills with patients and staff; demonstrates proper telephone techniques and etiquette; acts as an escort to any patient or family member needing directions; shows sensitivity to differences of culture; demonstrates a positive and supportive manner in which patients / families/ colleagues perceive interactions as positive and supportive.
NewClinical Vendor Outsourcing Manager CRO Sourcing & Contracts Pyramid Consulting, IncClinical Vendor Outsourcing Manager CRO Sourcing & ContractsLos Angeles, CA$66–$71 / hourKey Requirements and Technology Experience: 5+ years of relevant experience in clinical vendor outsourcing, clinical sourcing, CRO management, clinical contracts, procurement, or related pharmaceutical/biotechnology functions. Key Responsibilities: Lead and support end-to-end sourcing and contracting activities for full-service CROs and clinical vendors supporting clinical development programs.
Clinical Trials Site Director - Multiple Locations Nationwide Headlands Research IncClinical Trials Site Director - Multiple Locations NationwideCAThis general interest posting is designed for Site Directors who may not see a current opening that aligns with their location-but who would like to be considered for future leadership opportunities across our growing network of clinical research sites nationwide. Our Site Directors play a critical role in driving site performance, leading cross-functional teams, and ensuring the successful execution of clinical trials in a compliant, patient-centered environment.
Clinical Operations Specialist I – Clinical Trials & Device Management (Onsite, Irvine, CA) Manpower EngineeringClinical Operations Specialist I – Clinical Trials & Device Management (Onsite, Irvine, CA)Irvine, CA$30–$35 / hourTemporaryp> ManpowerGroup® (NYSE: MAN), the leading global workforce solutions company, helps organizations transform in a fast-changing world of work by sourcing, assessing, developing, and managing the talent that enables them to win. We are recognized consistently for our diversity - as a best place to work for Women, Inclusion, Equality and Disability and in 2022 ManpowerGroup was named one of the World's Most Ethical Companies for the 13th year - all confirming our position as the brand of choice for in-demand talent.
Spec 1, Clinical Operations LancesoftSpec 1, Clinical OperationsIrvine, CA$35G., clinical study teams, Manufacturing Operations, Finance, Supply Chain, Quality, and Compliance groups) to develop and lead the execution of the device process, and ensuring continuous process improvement of efficiency and accuracy of processes and procedures. Confirm receipt of study product at clinical sites and tracks product through to final disposition;ensuring required documentation are filed in the Trial Master File (TMF).
Clinical Operations Spec 1 LanceSoft IncClinical Operations Spec 1Irvine, CA$35–$40 / hourEnsure compliance with regulations and manage the lifecycle of devices, while closely partnering with other internal key stakeholders ( e.g., clinical study teams, Manufacturing Operations, Finance, Supply Chain, Quality, and Compliance groups) to develop and lead the execution of the device process, and ensuring continuous process improvement of efficiency and accuracy of processes and procedures. Identify, develop, recommend, and implement, moderately complex process development and process improvement solutions to optimize global trial workflow timelines, (e.g., device return aging issues, status of open device issues/queries, etc.).
Clinical Informatics Analyst Circuit Clinical Solutions IncClinical Informatics AnalystCARemote$25–$35 / hourTopping a long list of innovation and startup awards over the last 5 years - including winning SCOPE's Participant Engagement Award and winning at 43North - Circuit recently won Fast Company's World Changing Ideas Award. Happy: we seek pragmatic optimists - pessimism and ironic dispositions, especially in leadership can kill startups - we seek those who know the world can be improved by those who work hard and smart to change it.
NewAssistant or Associate Professor of Clinical Neurological Surgery (Neuro-Oncologist) University of Southern CaliforniaAssistant or Associate Professor of Clinical Neurological Surgery (Neuro-Oncologist)Los Angeles, CA$275,000–$400,000 / yearThe successful candidate will also work with relevant clinical and research programs to develop new clinical service lines that provide comprehensive, multidisciplinary care for patients with primary and metastatic brain and spinal cord tumors and neurological complications of cancer and cancer-directed therapies. In collaboration with relevant programs at Keck Medicine of USC and the USC Norris Comprehensive Cancer Center, the candidate will help develop scholarly programs and a well-balanced clinical trial portfolio that advances the care of patients with primary and metastatic brain and spinal cord tumors.
NewLead-Data Engineer St. Jude Children's Research Hospital IncLead-Data EngineerCARemote$94,640–$169,520 / yearServe as a technical lead for data modernization and digital transformation initiatives, including the Clinical Research Workbench and broader data modernization efforts, by providing architectural guidance, driving adoption of modern data and AI technologies, identifying opportunities for process innovation, and ensuring alignment with institutional research, analytics, governance, and operational objectives. In addition to technical leadership, the Lead Data Engineer is expected to drive strategic data initiatives, proactively identify opportunities for process improvement, automation, AI adoption, and data modernization, and provide expert guidance on emerging technologies that support clinical research and institutional objectives.
Sr. Clinical Trials Associate II Glaukos CorpSr. Clinical Trials Associate IIAliso Viejo, CAClinical site and vendor management: oversee communication with clinical sites and vendors, managing site activities such as initiation, monitoring, and close-out visits, and proactively resolving site-related issues. Cross-functional leadership: act as a liaison with Clinical Operations, CMC, Finance, Business Systems, and research teams, aligning project objectives and supporting efficient, high-quality study operations.
Nurse Practitioner / Physician Assistant Modena Allergy + AsthmaNurse Practitioner / Physician AssistantLaguna Niguel, CaliforniaModena Health (“MH”) and Modena Allergy & Asthma ("MAA") are leading and rapidly growing medical practices specializing in allergy, asthma, and immunology care, with clinics across Southern California and Arizona—and ambitious plans for national expansion. As an Allergy and Asthma NP/PA, you will be responsible for providing direct patient care, performing assessments, diagnosing, and managing the treatment of patients with allergic conditions, such as allergic rhinitis, asthma, eczema, food allergy, amongst others.
Director, Clinical Site Velocity Clinical Research IncDirector, Clinical SiteVan Nuys, CA$140,000–$160,000 / yearThe Clinical Site Director oversees and manages all aspects of the clinical trial process including study feasibility, clinic staffing, patient recruitment, study conduct and regulatory compliance. We are committed to making clinical trials succeed by generating high quality data from as many patients as possible, as quickly as possible while providing exemplary patient care at every step.
Director, Clinical Site Velocity Clinical Research, Inc.Director, Clinical SiteVan Nuys, California$140,000–$160,000 / yearFull timeThe Clinical Site Director oversees and manages all aspects of the clinical trial process including study feasibility, clinic staffing, patient recruitment, study conduct and regulatory compliance. Overview: Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites.
Sub-Investigator (NP or PA) - Long Beach Irvine Clinical ResearchSub-Investigator (NP or PA) - Long BeachLong Beach, CAFull timeCollaborative Research Team: Partner closely with Principal Investigators, fellow Sub-Investigators, clinical research coordinators, and study raters to ensure quality trial delivery. The clinician will oversee and conduct clinical trials of some of the most promising drugs under investigation in Alzheimer's Disease treatment and prevention, driving clinical excellence at our growing Long Beach site.
Principal Investigator CenExelPrincipal InvestigatorLos Alamitos, CaliforniaMedical knowledge and ability to provide clinical information to study teams; Knowledge of medications and general medical conditions; Knowledge and Understanding of GCP/ICH guidelines. Evaluate participants for clinical research trials based on their past medical history in comparison to the protocol specific inclusion and exclusion criteria.
NewPatient Care Assistant - 5E Telemetry - Part Time 12 Hour Days (Non-Exempt) (Union) University of Southern CaliforniaPatient Care Assistant - 5E Telemetry - Part Time 12 Hour Days (Non-Exempt) (Union)Los Angeles, CaliforniaPerforms essential skills which contribute to positive patient outcomes per routing, MD orders, and RN direction • Vitals • Daily weight • I & O • Hygiene: bath, peri-care, oral care, HS care, hair care • Maintains clear and organized patient rooms • Assist with meals/feeding • Ambulation/mobility; turn bed patients every 2 hours, transfers from bed to chair • Provides fresh water at beginning and end of shift and prn • Appropriately prioritizes patient needs. Communication: • Makes presence known before entering a room or private area • Identifies/introduces self to patient and visitors • Explains plan of care to the patient • Does not engage in inappropriate discussions regarding other patients and unit operations • Knows and utilizes all computerized systems to send messages, document care, and communicate patient/unit needs to various departments.