Serve as primary operational contact and mentor junior staff for global Phase 1-3 trials.
Jade Biosciences is a clinical-stage biotechnology company developing best-in-class therapies for autoimmune diseases. It is a small, dynamic company offering an exciting opportunity to contribute to its immunology pipeline.
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.
Serve as scientific lead for clinical programs, supporting trial design, execution, data interpretation, and regulatory activities.
Collaborate with cross-functional teams including Clinical Operations, Biostatistics, Regulatory Affairs, and external partners.
Contribute to scientific publications, regulatory submissions, and relationships with investigators and key opinion leaders.
The company is a clinical-stage organization advancing innovative regenerative therapies for significant unmet needs in ophthalmology. It fosters a collaborative, high-performance culture with mentorship and professional growth opportunities.
Lead chemistry efforts on cross-functional project teams to drive PROTAC programs from inception to clinical candidate nomination.
Design molecules with optimized potency, selectivity, and pharmacokinetic properties, focusing on degrader-antibody conjugates.
Collaborate with computational chemistry, CROs, and cross-functional partners to analyze SAR and inform strategic decisions.
Arvinas is a biotech company developing therapies that degrade disease-causing proteins via its proprietary PROTAC platform. It is a passionate, curious team headquartered in New Haven, CT, driven to improve patients' lives.
Conduct and report all types of onsite monitoring visits.
Perform CRF review, source document verification, and query resolution.
Support study startup, site communication, and audits.
PSI is a leading CRO with 30+ years in the industry, offering stability and innovation. We focus on quality and on-time services across therapeutic indications, with friendly and supportive colleagues.
Design and execute stability studies across the gummy portfolio, tracking timepoints and sharing data with stakeholders.
Validate analytical methods, identify detection limits, and negotiate with external testing labs.
Own the complete documentation suite for every SKU, ensuring audit-ready specs and paper trails.
This high-growth product organization develops a diverse gummy supplement portfolio. They operate as a fully remote, high-trust team with biannual in-person off-sites.
Lead real-world evidence programs and health economics models to demonstrate Virta's clinical and economic value.
Translate complex claims and clinical data into actionable insights that drive commercial growth and product innovation.
Publish findings in peer-reviewed journals and present evidence at conferences while partnering cross-functionally.
Virta Health is on a mission to reverse metabolic disease in one billion people through technology, personalized nutrition, and virtual care. Backed by over $350 million from top-tier investors, the remote-first company partners with major health plans and employers, fostering a values-driven culture.
Monitor clinical investigative sites to ensure protocol execution and regulatory compliance.
Conduct site qualification, initiation, interim monitoring, and closeout visits for Phase 1-4 studies.
Train site personnel, manage investigator payments, and identify new investigators and sites.
AbbVie discovers and delivers innovative medicines and solutions across immunology, oncology, and neuroscience. It is a global biopharmaceutical company committed to integrity, innovation, and transforming lives.
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.
Serve as study statistician for Phase 1-3 vaccine clinical trials, leading statistical design, analysis, and reporting.
Oversee statistical CROs, develop analysis plans, and ensure regulatory and scientific rigor.
Provide statistical consultation across CVIA programs and represent PATH at scientific meetings.
PATH is a global nonprofit dedicated to achieving health equity, developing and scaling innovative solutions to pressing health challenges. With more than 40 years of experience, PATH fosters a culture of collaboration and partnership across diverse teams.