Set enterprise strategy for clinical pharmacology, pharmacometrics, and model-informed drug development across Recursion’s clinical portfolio.
Own dose strategy from first-in-human through registrational development, including dose escalation, optimization, and label-supporting dose justification.
Lead quantitative development approaches including population PK, PK/PD, exposure-response, PBPK, QSP, and clinical trial simulations.
Provide clinical pharmacology expertise for regulatory submissions and development documentation.
Lead analysis, interpretation, and reporting of clinical PK/PD data for assigned projects.
Collaborate across functions and oversee CROs to support clinical development milestones.
They are a clinical-stage biotechnology company developing innovative therapies for rare and inherited diseases. They operate with a collaborative, cross-functional team culture centered on rigorous science and patient-focused development.
Lead global CMC regulatory strategy for the portfolio, including Phase 3 readiness and launch planning.
Serve as the company's lead CMC voice with FDA, EMA, and other global health authorities.
Build, lead, and develop a high-performing CMC Regulatory team as the company scales.
Kailera Therapeutics is a biopharmaceutical company developing novel therapies for obesity and related conditions. The company has an entrepreneurial, team-oriented culture and is passionate about creating an inclusive workplace.
Provide strategic medical leadership for clinical safety across investigational therapies for pulmonary fibrosis.
Conduct hands-on medical review of serious adverse events and lead signal detection and benefit-risk assessments.
Oversee cross-functional safety review meetings and regulatory interactions.
The company is a clinical-stage biotechnology firm developing innovative therapies for pulmonary fibrosis and other serious respiratory diseases. It is a growing, lean organization with a focus on pharmacovigilance infrastructure and global clinical development.
Provide strategic leadership and operational oversight for clinical trial design, analysis, and reporting.
Build and mentor a high-performing clinical biostatistics team while driving regulatory submissions.
Partner with cross-functional teams and vendors to ensure high-quality statistical and data management support.
Enveda is a clinical-stage, AI-enabled biotech discovering medicines from nature four times faster than industry standard. With over $845M in total funding and a $2B valuation, the company is recognized as a top startup employer and has three oral medicines in the clinic.
You build clinical pipelines for pharmacists, technicians, and leaders in the UK and Netherlands.
You own full-cycle recruitment: sourcing, screening, checks, and closing.
You manage agencies and partner with clinical ops to scale without bottlenecks.
AIOS is building the world’s first full-stack AI doctor, serving 200k monthly patients via Bolt Pharmacy. We're a profitable, founder-led company at $450M ARR, growing rapidly with a young and intense culture.
Own CMC strategy and execution across the full portfolio, spanning drug substance, drug product, device/combination products, and oral solid dose formulations.
Lead process development, scale-up, technology transfer, and regulatory submissions for CMC and device sections to support global filings.
Build and mentor a high-performing CMC and device engineering organization while partnering cross-functionally with Regulatory, Quality, Clinical, and Commercial teams.
Kailera Therapeutics is a late clinical-stage biotechnology company advancing a pipeline of GLP-1-based therapies for obesity and related conditions, including injectable and oral candidates in global trials. The company fosters an entrepreneurial, team-oriented culture focused on collaboration, integrity, and excellence as it scales toward commercial launch.
Provide strategic and operational leadership across multiple clinical programs, translating development strategy into strong execution.
Oversee clinical trial planning, budgets, CRO/vendor relationships, and cross-functional collaboration to ensure quality and accountability.
Lead and develop a small Clinical Operations team while remaining hands-on in a fast-paced biotech environment.
Deciphera, a member of Ono Pharmaceutical Co., Ltd., is a biopharmaceutical company focused on discovering, developing, and commercializing new medicines for cancer, neurologic, and autoimmune diseases. The company fosters an inclusive culture valuing curiosity, creativity, and shared accountability, empowering employees to drive breakthroughs.
Develop and lead enterprise-wide participant recruitment strategies to improve enrollment performance and accelerate study timelines across a multi-site clinical research network.
Drive participant funnel optimization, enrollment forecasting, and data-driven decision-making to enhance recruitment predictability and efficiency.
Spearhead cross-functional transformation roadmaps, platform adoption, and process improvement initiatives in partnership with Clinical Operations, Marketing, and Systems & Analytics.
Headlands Research is a network of next-generation clinical trial sites that integrates technology and high-quality support services to make clinical research accessible to participants. Founded in 2018, the company operates 20+ sites across the US and Canada and continues to grow its network and centralized capabilities.
Provide operational leadership for clinical research programs, developing strategies for timelines, enrollment, and risk mitigation.
Manage external budgets up to $200 million and lead cross-functional innovation initiatives for process improvement.
Mentor and develop clinical operations staff, including supervision of 4–15 study managers and up to 30 indirect reports.
AbbVie discovers and delivers innovative medicines and solutions for serious health issues in immunology, oncology, neuroscience, and aesthetics. The company is a large global organization that values integrity, inclusion, and innovation.
Lead the strategy, planning, execution, and maintenance of safety databases and outsourced PV activities.
Oversee collection, evaluation, and reporting of safety data from clinical trials, shaping the safety governance framework.
Manage PV vendor contracts, quality/compliance for ICSR case processing, and mentor PV operations associates.
MapLight Therapeutics is a clinical stage biotech company focused on drug discovery for central nervous system disorders. It is a growing organization that values open dialogue and mutual respect while developing novel therapies for psychiatric symptoms.
Provide strategic statistical leadership across oncology development programs, collaborating with Clinical Development, Regulatory, Medical, Commercial, and Portfolio teams.
Design and validate trial types, endpoints, and innovative adaptive designs while performing sample size/power calculations and establishing go/no-go decision gates.
Support regulatory submissions and health authority interactions, and quantify technical success probability for pipeline prioritization.
We are a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. With over 4,000 professionals in more than 20 countries, we are committed to training, diversity, and accelerating innovative drug and device development.
Lead biostatistics function for oncology clinical trials, including study design and statistical analysis.
Partner with clinical and regulatory teams to author key documents and ensure data quality.
Represent biostatistics in interactions with CROs and regulatory agencies to ensure project success.
Summit Therapeutics Inc. is a biopharmaceutical oncology company focused on improving quality of life. They have multiple global Phase 3 clinical studies and a team of world-class professionals driven by core values of integrity, passion, and collaboration.
Lead and scale the Clinical Operations function for MiraVi's ophthalmology programs.
Drive global clinical operations strategy, CRO/vendor oversight, and study execution from startup to close-out.
Partner with regulatory, CMC, quality, and finance to deliver compliant, on-time, on-budget trials.
MiraVi is an ophthalmology affiliate of Osanni focused on advancing treatments for dry age-related macular degeneration (AMD). The company is building a highly skilled, collaborative team dedicated to developing new medicines for patients.