Medical Director, Clinical Research, Endocrinology Crinetics Pharmaceuticals IncMedical Director, Clinical Research, EndocrinologyCA$270,000–$298,000 / yearCollaborate with Medical Affairs and Commercial members to develop effective working relationships with key investigators, key opinion leaders and patient advocates to optimize scientific quality/innovation of clinical study design, execution, reporting and publication. Provide scientific and clinical direction for the development of clinical protocols (and, in early stages, clinical trial outlines [CTOs] and synopses), amendments, and related documents (e.g., informed consent), working with Medical Writing to ensure content accuracy and medical integrity.
Manager, Clinical Finance CondorManager, Clinical FinanceSan Diego, New YorkWe’re looking for experienced operators, passionate leaders, and industry mavericks who are not afraid to collaborate across traditional silos to solve complex problems with a strong desire to drive innovation in the biotech industry. Assumption Building: Collaborate with cross-functional teams to build and understand key trial assumptions within Condor, facilitating informed financial decision-making for clients.
Senior Clinical Research Associate ICON PlcSenior Clinical Research AssociateSan Diego, CA$110,520–$138,150 / yearWilling and able to travel up to 50% for on-site monitoring visits across southeast region; preference given to candidates residing in Seattle, Portland, Denver or Southern California near major HUB airports to support efficient regional travel. ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
Medical Director, Clinical Development, Psychiatry Neurocrine Biosciences IncMedical Director, Clinical Development, PsychiatrySan Diego, CA$254,600–$347,000 / yearAssist in the recruitment, training and development of the clinical teams; Identify and select clinical consultants; Work with Medical Affairs and external opinion leaders to secure new collaborators and present trial results; Identify resource requirements, assist in budget planning and personnel forecasting for clinical research programs; Interface with Research, Product Development and Business Development to assess new product opportunities, develop clinical research strategy and product development plans; Other duties as assigned. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, hyperphagia in Prader-Willi syndrome, 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.
Director, Clinical Development Acadia Pharmaceuticals IncDirector, Clinical DevelopmentSan Diego, CA$230,900–$288,600 / yearWe are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. Resumes sent to Acadia employees in the absence of an executed search agreement will not obligate Acadia in any way with respect to the future employment of those individuals or potential remuneration to any recruiter or search firm.
Senior Director, Clinical Operations Travere Therapeutics IncSenior Director, Clinical OperationsSan Diego, CA$219,000–$285,000 / yearExcellent communication skills, both oral and written and is confident in developing materials and presenting to senior leadership (DRC, ET, PGT and BoD as applicable) as well as communicate key issues and mitigations to relevant cross-functional stakeholders. We stick by our values centered on patients, courage, community, and collaboration to pursue our vision of becoming a leading biopharmaceutical company dedicated to the delivery of innovation and hope to patients in the global rare disease community.
Associate Director, Clinical Quality Assurance Vera Therapeutics IncAssociate Director, Clinical Quality AssuranceSan Diego, CA$140,000–$210,000 / yearThe individual partners closely with Clinical Operations, Pharmacovigilance, Data Management, Regulatory Affairs, and other development function and serves as a key member of study teams, helping identify quality issues and risks, and reviews quality events, investigations, and CAPAs; analyzing quality signals across studies and vendors that support risk-based decision making, and ensuring quality management practices are appropriately implemented throughout the clinical trial lifecycle. Vera Therapeutics' lead product candidate is atacicept, a fusion protein self-administered at home as a subcutaneous once weekly injection that blocks both B-cell Activating Factor (BAFF) and A Proliferation-Inducing Ligand (APRIL), which stimulate B cells to produce autoantibodies contributing to certain autoimmune diseases, including IgA nephropathy (IgAN) and lupus nephritis.
Clinical Data Scientist Exagen Diagnostics IncClinical Data ScientistCarlsbad, CA$130,000–$160,000 / yearProvide clinical data management for studies sponsored by the Company and studies where Exagen serves as a central laboratory, including data management plans, data reconciliations, release of data clarification forms, query resolution, dataset locks, manual release of test reports, and preparation of reports for invoicing, in coordination with study sponsors and/or CROs. The CDS owns dataset curation and clinical database development across the Company's registry, biobank, and study data; applies machine learning and AI approaches-including large language model (LLM)-assisted workflows-in partnership with the data science team; and delivers analysis-ready data to biostatistics.
Associate Director, Clinical Trial Management Xencor IncAssociate Director, Clinical Trial ManagementSan Diego, CA$169,500–$203,250 / yearLeads a cross-functional study team to ensure all elements of the study are addressed proactively by the relevant parties, follows up on action items, proactively identifies and resolves operational issues and is accountable for the overall study performance, budget and timeline in accordance with the company corporate goals. Education/Experience/Skills: Position requires a Bachelor's degree in a field of science (such as Biology or Immunology) and at least 10 years of related experience, including 6 years in clinical trial management/clinical operations departments.
Oncology Clinical Development Scientist (Director) Pfizer IncOncology Clinical Development Scientist (Director)La Jolla, CA$176,600–$294,300 / yearFollow relevant SOPs and regulations, has an excellent understanding of and complies with applicable trainings, seeks opportunities to further improve quality and efficiency of clinical procedures; leads or actively participates in portfolio- and enterprise level workgroups aimed at optimizing PFE clinical development procedures; may be a subject matter expert or business process owner for a relevant SOP or procedure. Author protocols, study level informed consent documents, and contributes to authoring of IBs, site training materials, clinical study reports, regulatory responses, and other clinical and regulatory documents; supports preparations for Health Authority meetings, participates as appropriate.
Sr. Clinical Trial Manager Janux TherapeuticsSr. Clinical Trial ManagerSan Diego, California$165,000–$180,000 / yearThe role requires a deep understanding of clinical trial processes, regulatory compliance (GCP, FDA, ICH), and the ability to lead cross-functional teams to ensure high-quality, timely, and cost-effective trial execution. $165,000 - $180,000 a year In addition to a competitive base salary ranging from $165,000 to $180,000, we offer stock options, restricted stock units, a stock purchase plan (ESPP) and a target bonus.
MedTech Part Time Clinical Consultant – Tidewater, VA IQVIAMedTech Part Time Clinical Consultant – Tidewater, VACarlsbad, California3+ years’ experience with a strong clinical background in the Cardiac ICU (CICU), Cardiovascular ICU (CVICU), Cardiovascular OR (CVOR), or Catheterization Lab (Cath Lab) required; CVICU experience highly preferred. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
MedTech Part Time Clinical Consultant – Albany, NY IQVIAMedTech Part Time Clinical Consultant – Albany, NYCarlsbad, California3+ years’ experience with a strong clinical background in the Cardiac ICU (CICU), Cardiovascular ICU (CVICU), Cardiovascular OR (CVOR), or Catheterization Lab (Cath Lab) required; CVICU experience highly preferred. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
Senior Director, Clinical Operations Travere TherapeuticsSenior Director, Clinical OperationsSan Diego, CA$219,000–$285,000 / yearExcellent communication skills, both oral and written and is confident in developing materials and presenting to senior leadership (DRC, ET, PGT and BoD as applicable) as well as communicate key issues and mitigations to relevant cross-functional stakeholders. We stick by our values centered on patients, courage, community, and collaboration to pursue our vision of becoming a leading biopharmaceutical company dedicated to the delivery of innovation and hope to patients in the global rare disease community.
Women's Health Procedural Specialist / Clinical Educator IQVIAWomen's Health Procedural Specialist / Clinical EducatorCarlsbad, CaliforniaIndividuals are typically required to have completed/up to date: Measles, Mumps & Rubella vaccine, Varicella (chicken pox) vaccine, Negative Tuberculosis (TB) Test, Tetanus, Diphtheria & Pertussis (Tdap) vaccine, Hepatitis B vaccine, Influenza vaccine (seasonal), and COVID-19 vaccine primary series. Our Women's Health Procedural Specialists experience a unique opportunity to leverage their clinical expertise while supporting healthcare providers through education and training on innovative women's health technologies.
MedTech Part Time Clinical Consultant – Kansas City, Mo IQVIAMedTech Part Time Clinical Consultant – Kansas City, MoCarlsbad, California3+ years’ experience with a strong clinical background in the Cardiac ICU (CICU), Cardiovascular ICU (CVICU), Cardiovascular OR (CVOR), or Catheterization Lab (Cath Lab) required; CVICU experience highly preferred. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
MedTech Part Time Clinical Consultant – Paducah, KY/W. TN IQVIAMedTech Part Time Clinical Consultant – Paducah, KY/W. TNCarlsbad, California3+ years’ experience with a strong clinical background in the Cardiac ICU (CICU), Cardiovascular ICU (CVICU), Cardiovascular OR (CVOR), or Catheterization Lab (Cath Lab) required; CVICU experience highly preferred. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
MedTech Part Time Clinical Consultant – South Louisiana and NE Texas IQVIAMedTech Part Time Clinical Consultant – South Louisiana and NE TexasCarlsbad, California3+ years’ experience with a strong clinical background in the Cardiac ICU (CICU), Cardiovascular ICU (CVICU), Cardiovascular OR (CVOR), or Catheterization Lab (Cath Lab) required; CVICU experience highly preferred. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
MedTech Part Time Clinical Consultant – Naples, FL IQVIAMedTech Part Time Clinical Consultant – Naples, FLCarlsbad, California3+ years’ experience with a strong clinical background in the Cardiac ICU (CICU), Cardiovascular ICU (CVICU), Cardiovascular OR (CVOR), or Catheterization Lab (Cath Lab) required; CVICU experience highly preferred. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
MedTech Part Time Clinical Consultant – Wilmington, NC IQVIAMedTech Part Time Clinical Consultant – Wilmington, NCCarlsbad, California3+ years’ experience with a strong clinical background in the Cardiac ICU (CICU), Cardiovascular ICU (CVICU), Cardiovascular OR (CVOR), or Catheterization Lab (Cath Lab) required; CVICU experience highly preferred. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.