Owns technical stewardship of the existing product portfolio, ensuring compliance and manufacturability.
Leads qualification of alternate materials and executes reformulations to maintain product standards.
Drives cross-functional alignment with Operations, Supply Chain, QA, and PD Engineering.
Nordic Naturals is a dietary supplement company that develops and manufactures nutritional products. The company emphasizes a positive, accountable, and innovative work culture, fostering cross-functional collaboration.
Support Clinical Trial Managers with study start-up, protocol development, and Trial Master File preparation.
Coordinate with clinical sites on documentation, training, and compliance with FDA and GCP requirements.
Assist with tracking study payments and providing operational support across the full study lifecycle.
The company is a partner organization specializing in clinical research and development, operating through Jobgether. It offers a structured clinical operations environment with cross-functional teams and professional growth opportunities.
Lead end-to-end product development execution for new products and line extensions, from ideation to commercial launch.
Manage the innovation portfolio's stage-gate process, ensuring projects meet milestones on time and within scope.
Partner cross-functionally with R&D, Supply Chain, Marketing, Quality, and Regulatory teams to align on product specifications and launch readiness.
AG1 is a nutritional supplement company dedicated to providing foundational nutrition through science-backed products. They foster a high-performance culture with values like Radical Ownership and Continuous Pursuit of Excellence, operating remotely with a global team.
Lead analytical strategy and method lifecycle management for small molecule drug substance and drug product development.
Oversee external analytical partners, CDMOs, and testing laboratories to ensure cGMP compliance and quality.
Support regulatory submissions, specifications, stability programs, and commercialization readiness.
Mineralys Therapeutics is a clinical-stage biopharmaceutical company focused on developing medicines to target hypertension and related comorbidities such as chronic kidney disease and obstructive sleep apnea. The company is headquartered in Radnor, Pennsylvania and operates as a fully remote company.
Own clinical supply chain order fulfillment, including labeling, packaging, and distribution of trial products.
Build and lead Clinical Supply Chain, Planning, and Warehousing teams with full regulatory compliance.
Develop sourcing strategies and manage vendors to ensure cost-effective, uninterrupted supply.
RayzeBio, a wholly-owned subsidiary of Bristol Myers Squibb, develops transformative radiopharmaceutical therapies for cancer patients. The company blends the pioneering spirit of an emergent biotech with global oncology expertise, fostering a collaborative multidisciplinary team where every member makes an immediate impact.
Lead drug product CMC strategy for small molecule programs from early to late stage.
Oversee formulation, process development, scale-up, technology transfer, and validation.
Manage CDMOs and external partners to ensure quality, timelines, and supply continuity.
Our partner is a biotechnology company focused on advancing small molecule drug product development. They operate in a fast-moving, highly outsourced environment with a collaborative, patient-focused culture.
Collaborate with the Clinical Operations team to support timely conduct of clinical studies according to protocols, GCP, SOPs, and regulations.
Lead operational management for assigned regions and sites, including vendor management and oversight of CRO monitors.
Contribute to the development and maintenance of study documents and ensure the Trial Master File is complete and inspection-ready.
BridgeBio is a biopharmaceutical company founded to discover, create, test, and deliver transformative medicines for patients with genetic diseases and cancers with clear genetic drivers. Founded in 2015, the company has built a portfolio of 20+ drug development programs spanning preclinical to late-stage development across multiple therapeutic areas.
Manage end-to-end IRB meeting workflows, including submissions, reviewer assignments, and meeting preparation.
Facilitate communication among client services, IRB Chairs, Board members, and clients to ensure timely review processes.
Prepare and review informed consent forms for regulatory compliance and quality.
The company coordinates Institutional Review Board (IRB) meetings within a highly regulated clinical research environment. They offer a collaborative and inclusive culture focused on ethical, patient-centered outcomes, though company size is not specified.