Ich Jobs

Eli Lilly is hiring an Associate Director to lead analytical project management and technical transfers supporting manufacturing and laboratory governance.

Experienced Regulatory Affairs professional needed to lead preparation and coordination of regional regulatory submissions and labeling for investigational and commercial products at Gilead in Foster City.

Clinical Research Coordinator A/B needed at Penn's CCI to support coordination, documentation, and regulatory compliance for early-phase oncology cell and gene therapy trials.

AbbVie is recruiting a Safety Deliverable Manager to drive and author PST safety deliverables, ensuring high-quality, regulatory-compliant safety summaries and aggregate reports across product lifecycles.

Celerion seeks an experienced Clinical Data Manager in Tempe, AZ to manage clinical database setup, cleaning, query resolution, and sponsor-facing data management activities across early- to late-phase studies.

Care Access is hiring a Regulatory Operations Specialist to manage site-level IRB and regulatory activities for U.S. clinical trials in a remote, fast-paced environment.

Agilent is hiring a Clinical Research Associate to monitor investigator sites, ensure GCP-compliant trial conduct, and maintain TMF/eTMF while supporting study start-up through closeout.

ORIC Pharmaceuticals seeks a Regulatory Affairs Manager to drive timely, compliant regulatory submissions and support clinical oncology programs from its San Diego office.

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Hims & Hers is hiring a Quality Validation Specialist to lead commissioning, qualification, and calibration programs for a sterile cGMP manufacturing site and drive regulatory compliance and continuous improvement.

Experienced clinical monitor sought by Novartis to lead site monitoring for Phase I–IV trials in a remote, travel-heavy role ensuring data quality, regulatory compliance, and strong site relationships.

Lead and operationalize country-level study start-up activities for Novartis’ GDD portfolio, ensuring timelines, quality and regulatory compliance across a remote U.S.-based team.

Lead clinical and companion diagnostic compliance efforts at Grail by driving inspection readiness, audits, CAPA management, and cross-functional quality improvements to support clinical studies and CDx development.

Care Access is hiring an experienced Senior Region Manager for Florida to lead site operations, staff development, quality and growth across multiple clinical research sites.

Clinical Research Associate needed to manage and monitor early-phase medical device and imaging trials, ensuring regulatory compliance and high-quality clinical data collection across domestic and international sites.

ICON seeks a remote Clinical Research Associate to perform site qualification, monitoring, and close-out activities for ophthalmology clinical trials across the Northeast region.

Experienced medical writer needed to author and QC safety sections of Phase I/II clinical study reports for a US-based, remote role at Celerion.

Experienced clinical supply professional needed to manage forecasting, IRT operations, vendor coordination, and depot/site inventories for Cogent Biosciences' clinical programs.

Experienced clinical operations leader needed to manage and develop a global team of Site Management Leads and drive consistent, data-driven site management strategy across therapeutic programs at AbbVie.

Cogent Biosciences seeks an experienced Clinical Trial Manager to lead operational delivery of pivotal rare-disease and oncology trials for its precision kinase inhibitor programs.

Experienced analytical scientist needed to develop and validate LNP-focused analytical assays and support platform and drug-product characterization at an early-stage RNA therapeutics venture backed by Fapon Biotech.

Senior medical writer and team lead role responsible for authoring regulatory submissions and maturing medical writing processes at a growth-stage biotech focused on immunology.

Eliquent Life Sciences is hiring a Supplier Quality Consultant to lead supplier qualification, audits, and compliance activities for pharmaceutical and biopharmaceutical clients.

AbbVie is recruiting a seasoned Medical Director to lead the design, execution, and interpretation of complex neuroscience clinical development programs and to serve as an in-house clinical expert.

BlueRock Therapeutics is hiring a Director of Clinical Operations Quality to lead SOP and TMF standards, drive clinical compliance and inspection readiness across its advancing cell therapy clinical programs.

Experienced publishing specialist needed to manage eSubmission workflows, ensure regulatory-compliant clinical document publishing, and support process and vendor management at AbbVie's North Chicago site.

Provide medical leadership for oncology clinical trials at AbbVie, overseeing protocol design, safety assessment, and cross-functional execution to support product development strategy.

Natera is hiring an experienced Sr. Clinical Biospecimen Operations Associate to manage biospecimen operational activities and drive study execution and sample quality across clinical trials.

Lead enterprise CMC strategy and cross-functional teams at Bristol Myers Squibb to turn molecules into medicines across small molecules, biologics and new modalities.

Experienced clinical trial manager needed to lead global, late-stage neuroscience studies with accountability for timelines, budgets, quality, and regulatory readiness.

Experienced clinical project manager needed to lead sponsor-dedicated biomarker and bioanalytical study operations in a fully remote role at a global CRO.

Senior PV leader needed to drive operational excellence, program delivery, and regulatory-ready processes for Novartis' US pharmacovigilance organization.

A Scientist in AS&T to lead and support analytical method development, transfers, validation, and compliance activities for Novartis’ Morris Plains Quality operations.

Lead an analytical development team at AbbVie to design and implement robust separation-based methods and regulatory-ready analytical strategies supporting biologics development and GMP testing.

Arsenal Biosciences is hiring an experienced Biosample Manager to lead clinical biosample lifecycle operations and vendor management for translational studies in South San Francisco.

Altasciences is hiring a Senior Clinical Research Associate to lead and perform site monitoring, ensure data quality and compliance, and mentor clinical staff across investigator sites.

Crinetics Pharmaceuticals is hiring a Senior Manager to lead clinical data management, SAS programming and external data validation and reporting to support clinical development and regulatory readiness.

Kite is hiring a Director of GxP Auditing to lead the global audit program, ensuring GMP/GLP compliance and inspection readiness across internal operations and external partners.

Precision for Medicine is hiring experienced Oncology CRAs (CRA II / Sr. CRA) to monitor clinical studies remotely while supporting study start-up, site oversight, and client interactions with up to ~50–60% domestic travel.

Lead scientific oversight and data-quality activities for late-stage oncology Phase 3 trials at Pfizer, partnering cross-functionally to drive study execution and regulatory readiness.

Lead and coordinate Pfizer’s early-stage oncology clinical programs from FIH through proof-of-concept, driving protocol development, data review, and cross-functional execution.

Lead end-to-end operational delivery of complex autoimmune clinical trials at Janux Therapeutics, ensuring timelines, budgets, and regulatory compliance.

Gilead is hiring a Clinical Trials Manager in Foster City to oversee international clinical trial operations, CRO oversight, and cross-functional study delivery.

Lead clinical science initiatives at Deciphera Pharmaceuticals to support and advance oncology drug development programs through collaborative cross-functional efforts.

AbbVie is looking for an experienced Program Lead II to drive clinical program execution and strategy within their Development Operations team.

A Clinical Research Associate role at Saint Michael's Medical Center focused on coordinating clinical trials and supporting research compliance within a leading healthcare institution.

A Mobile Research Nurse role supporting clinical research in Colorado Springs, offering flexible, remote contract work with competitive compensation.

Eurofins Scientific is looking for a Sample Coordinator to manage laboratory sample workflows and support cGMP-compliant operations in Holly Springs, NC.

Lead clinical development efforts at Noven Pharmaceuticals by managing clinical programs, regulatory compliance, and cross-functional collaboration for global clinical trials.

Lead Eurofins' regulatory and quality assurance teams to drive compliance and operational excellence in the pharmaceutical CRO industry.

Seeking a compassionate Mobile Research Nurse to administer investigational treatments and conduct patient assessments in dynamic clinical research projects.