Ich Jobs

Lead clinical science for oncology-focused, early-to-late stage studies at Bicycle Therapeutics, driving protocol design, data interpretation, regulatory writing, and cross-functional execution.

Lead and execute global medical and scientific communications for BlueRock's neurology and ophthalmology cell therapy programs, ensuring high-quality, compliant publications, congress strategy, and KOL engagement.

Lead a hybrid Support Operations team at AbbVie's Lake County site, overseeing case initiation, data entry and reconciliation while ensuring compliance and operational excellence.

Lead the development and quality control of clinical and regulatory documents at AbbVie, applying deep scientific knowledge and regulatory expertise to drive successful submissions.

Vertex is hiring a hybrid contract Project Manager with CDMO and tech-transfer experience to lead cross-functional CMC projects supporting cell and gene therapy development.

WHOOP is hiring a Project Manager, Clinical Trials to lead execution and operational oversight of WHOOP-sponsored clinical studies validating digital biomarkers and supporting regulatory pathways.

AbbVie is hiring a Lead Principal Medical Safety Analyst to lead vendor oversight for pharmacovigilance case processing and ensure compliant, high-quality adverse event management.

Experienced analytical science SME needed to lead development, validation, and network implementation of rapid microbiology safety methods for Vertex’s biologics and cell & gene therapy commercial programs on a 24-month part-time contract.

Lead and build clinical and commercial supply chain strategy and operations at ORIC to ensure compliant, cost-effective delivery of investigational and commercial drug product across global trials and launch readiness.

Lead and operationalize patient engagement strategies on AbbVie's ARC/Patient Council platform to improve equitable clinical trial access and enhance stakeholder and patient experiences.

Lead site management and monitoring activities for clinical studies at Exact Sciences, ensuring protocol adherence, regulatory compliance, and strong sponsor-site relationships in a remote field-based role.

AbbVie is hiring a seasoned Clinical Operations leader to drive program-level strategy and execution for global clinical studies while developing operational talent and ensuring compliance.

Part-time Biostatistician I (Colorado-based, remote) to support clinical trial design, SAS programming, and statistical analyses across therapeutic areas.

Telix Pharmaceuticals is hiring a seasoned Medical Writer to lead and produce regulatory and clinical documentation for global submissions supporting its oncology and rare‑disease radiopharmaceutical portfolio.

AbbVie is hiring an experienced Occupational & Environmental Toxicologist to lead product and workplace risk assessments across development stages at its North Chicago site.

Lead technical strategy and execution for cell line development and tech transfer, delivering robust CLD and upstream process transfers to pharmaceutical and biotech partners from Asimov’s Boston site.

Lead clinical data management for assigned programs at Moderna’s Cambridge site, driving data quality, vendor oversight, and cross-functional alignment to deliver inspection-ready results.

Moderna is hiring an Associate Director in R&D Quality to lead vendor quality agreements, metrics, audits, and CAPA activities to enhance vendor oversight and inspection readiness.

Lead the implementation of AbbVie’s clinical trial diversity and inclusion strategy, partnering cross-functionally to increase diverse investigator and patient representation across the clinical portfolio.

ORIC Pharmaceuticals is hiring a Senior Clinical Trial Manager to lead global oncology trials, manage vendors/CROs, and drive study execution from start-up through database lock in a hybrid San Diego role.

Clinigen seeks an experienced Quality Operations Manager to lead on-site Quality Assurance operations and QMS implementation at CSM USA, ensuring regulatory compliance and operational excellence.

AbbVie is hiring a Study Project Manager II to lead end-to-end clinical study operations, drive strategic planning and execution, and ensure compliant, timely delivery across study phases.

MindMed is hiring an experienced Project Manager in the Programs and Portfolio Office to drive planning, execution, and cross-functional alignment for strategic clinical and development projects.

Apellis Pharmaceuticals seeks an experienced Clinical Trial Manager to lead clinical trial execution, vendor oversight, and trial documentation for programs across therapeutic areas.

Bristol Myers Squibb seeks a Clinical Scientist in Hematology to design and execute assigned clinical trial activities and contribute medical and scientific input across study deliverables.

QRC Group is hiring a bilingual Technical Writer in Gurabo to produce and maintain GMP- and regulatory-compliant documentation supporting pharmaceutical development, manufacturing, and inspections.

AbbVie is hiring a Safety Deliverable Manager to lead the creation, quality review, and delivery of regulatory aggregate safety documents that support product benefit-risk assessments.

Support community-based clinical trials by performing phlebotomy, specimen handling, participant interactions, and study operations across local clinics and outreach events in the Boston area.

Care Access is seeking an experienced Travel Clinical Research Coordinator based in Charleston, SC to manage protocol-compliant participant screening, enrollment, and study operations while traveling to sites nationwide.

Care Access is hiring an entry-level Clinical Research Assistant for the Future of Medicine program to conduct venipuncture, process specimens, support community recruitment events, and maintain study documentation in Union, NJ and nearby regions.

Experienced clinical operations professional needed to lead end-to-end study delivery and operational strategy for immunology clinical trials at AbbVie in a remote capacity.

AbbVie is hiring a Study Project Manager I in Immunology to lead end-to-end clinical study operations, driving quality, timelines and cross-functional collaboration for global trials.

Catalent is hiring an on-site Associate Scientist in Winchester, KY to support analytical method development, validation, and routine release/stability testing for clinical and registration programs.

Experienced analytical instrumentation specialist needed to lead validation, qualification, and method transfers for QC instruments in a regulated life-sciences environment.

Experienced pharmacovigilance or medical writing professional needed to manage and author high-quality safety deliverables for AbbVie's Product Safety Team across global regulatory frameworks.

AbbVie is hiring a Clinical Research Associate II to lead site monitoring and engagement efforts in support of clinical trial execution and data quality in the Dayton, OH area.

AbbVie seeks a Senior Clinical Research Associate to lead site monitoring activities, ensure protocol and regulatory compliance, and mentor CRAs in support of world-class clinical trials.

AbbVie is hiring a Study Project Manager I to lead cross-functional clinical study teams and drive operational excellence across study planning, execution and vendor management.

AbbVie is hiring a Study Project Manager I to lead cross-functional clinical study teams and drive high-quality, on-time execution of clinical research across development stages.

Care Access is hiring a Clinical Research Assistant in Miami to support community-based clinical trials through specimen collection, participant engagement, and study operations.

Holy Cross Hospital is hiring an on-site Registered Nurse Clinical Research Associate to support oncology clinical trials by coordinating patient recruitment, data collection, regulatory compliance, and safety reporting.

Experienced QA professional needed to lead inspection readiness and regulatory response activities for a consultancy supporting pharmaceutical and medical device clients.

Rho is hiring a board-certified Psychiatrist to serve as a remote Medical Director responsible for medical monitoring, safety review, and clinical development input across global clinical trial programs.

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.