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• Lead and oversee complex clinical trial operations from initiation through closeout.
• Serve as primary operational contact for industry-sponsored trials, ensuring quality and compliance.
• Mentor clinical operations managers and drive process improvements across projects.

This is a clinical research organization managing industry-sponsored trials and providing endpoint and specialty services. It emphasizes collaboration, flexibility, and operational excellence in a remote-first environment.

• Manage all clinical operational aspects of global trials including start-up, conduct, and close-out.
• Oversee CRO and site adherence to GCP and SOPs, proactively identifying and resolving study risks.
• Lead study team meetings, build investigator relationships, and support protocol development.

Vera Therapeutics is a commercial-stage biotech focused on transforming autoimmune disease treatment, starting with the kidney. Founded in 2016 in Brisbane, CA, the company values empathy, ownership, clarity, and urgency in a collaborative, fast-paced team.

• Support planning and operational execution of clinical trials, coordinating across sites, CROs, vendors, and teams.
• Manage vendor oversight, budgets, timelines, risks, and documentation ensuring GCP compliance.
• 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.

• Lead and coach a team of Clinical Study Operations professionals overseeing device-based clinical trials from feasibility to close-out.
• Drive domain-level ClinOps initiatives including process standardization, tooling, and data quality improvements.
• Represent ClinOps in business development conversations, feasibility discussions, and Investigator Meetings, ensuring operational readiness.

Beacon Biosignals transforms precision medicine for the brain, offering at-home EEG and diagnostic platforms for neurological, psychiatric, and sleep disorders. They are a remote-first, distributed company with hubs in Boston, New York, and Paris, emphasizing curiosity, sound judgment, and empathy.

• Oversee EMEA clinical trial operations, partnering with CROs and sites to ensure compliance and timely execution.
• Lead regional regulatory submission strategies and proactively resolve operational challenges to maintain study timelines.
• Mentor junior team members, review data and TMF documentation, and provide regular study updates to stakeholders.

Akero Therapeutics, a Novo Nordisk company, is a clinical stage biopharmaceutical company focused on developing transformative treatments for metabolic diseases. The company fosters a collaborative culture of problem solvers dedicated to bringing bold scientific approaches to patients.

• Serve as the primary clinical point of contact with clients, overseeing the operational portion of clinical studies per scope of work.
• Develop study-related clinical documents, train CRAs and vendors, and lead internal clinical team meetings to ensure trial compliance.
• Drive site feasibility, recruitment and retention strategies, and manage eTMF, budgets, and vendor oversight to ensure quality and timelines.

Precision for Medicine is a CRO that integrates clinical trial execution with deep scientific knowledge, laboratory expertise, and advanced data sciences to improve the speed, cost, and success rate of bringing life-changing therapies to patients, with a strong focus on Oncology and Rare Disease. The company combines new technologies, operational scale, and a collaborative environment to support the life sciences industry.

• Lead the development and execution of clinical development plans for exploratory and biopharmaceutics programs.
• Oversee global clinical trial operations, including timelines, budgets, vendors, and cross-functional collaboration.
• Drive risk management and strategic decision-making across the molecule lifecycle.

The hiring company is a pharmaceutical organization focused on clinical development and biopharmaceutics. It values learning agility, innovation, inclusion, and collaboration in a virtual and matrixed environment.

• Lead clinical study strategy and execution for regulatory approvals and evidence initiatives.
• Partner with stakeholders, investigators, and KOLs to design protocols and manage study progress.
• Oversee monitoring, compliance, and data analysis while mentoring junior staff.

Intuitive is a global leader in robotic-assisted surgery and minimally invasive care, known for da Vinci and Ion systems. Its team of engineers, clinicians, and innovators works to make surgery smarter, safer, and more human.

• Lead Clinical Trial Liaison performance, development planning, and quality delivery across EMEA.
• Oversee vendor-provided staff, implement standardised feasibility and site selection processes, and build investigator relationships.
• Report monthly metrics, escalations, and best practices while retaining a 15% liaison workload.

Regeneron is a leading biotechnology company that invents life-transforming medicines for people with serious diseases. Founded and led for over 30 years by physician-scientists, the company has a culture of innovation and has been recognized as a Great Place to Work.

• Lead and manage the assigned clinical operations team, setting and executing departmental strategy.
• Oversee clinical trial agreements, budgets, and the timely execution of clinical research programs from conception through final study report.
• Maintain oversight of study conduct at sites, ensure adherence to protocols and GCP, and serve as company representative at external meetings.

Iovance Biotherapeutics is the global leader in innovating, developing, and delivering tumor infiltrating lymphocyte (TIL) cell therapies for patients with solid tumors. As an end-to-end cell therapy company with fully owned, centralized U.S.-based manufacturing, it operates with a fast-paced, collaborative culture focused on bringing first-in-class treatments to cancer patients.

• Lead planning, execution, and oversight of clinical studies across Latin America.
• Act as primary client contact and ensure compliance with ICH-GCP, SOPs, and regulatory requirements.
• Mentor CRAs and partners while shaping country-level recruitment and monitoring strategies.

Precision Medicine Group provides clinical development, regulatory, and commercial solutions for life sciences companies. It fosters a collaborative, high-integrity culture with opportunities for growth and leadership in a global remote environment.

• Lead and oversee clinical data management activities across assigned studies, ensuring high-quality data in compliance with ICH-GCP and company SOPs.
• Manage CROs and external vendors, including database start-up, data cleaning, and database lock, while maintaining quality, timelines, and budget.
• Collaborate cross-functionally with Biometrics, Clinical Operations, Medical, and other teams to drive data management milestones and inspection readiness.

We are developing novel biologics designed to set a new standard for the treatment of chronic skin diseases like plaque psoriasis. As a Nasdaq-listed startup, we foster a vibrant, inclusive culture where everyone is encouraged to bring their authentic selves to work.

• Lead and oversee global Phase 0-4 clinical trials with cross-functional teams from inception to closure.
• Manage external vendors, recruitment strategies, and study systems to ensure quality, efficiency, and inspection readiness.
• Collaborate with study project managers to drive timelines, budgets, and compliance with ICH/GCP and AbbVie policies.

AbbVie discovers and delivers innovative medicines and solutions across immunology, oncology, neuroscience, and Allergan Aesthetics. They are a global, science-driven pharmaceutical company committed to integrity, innovation, and serving the community.

• Partner with cross-functional teams and study sites to support clinical operations across all trial phases.
• Perform remote monitoring of clinical trials and serve as secondary contact for sites supporting CRAs.
• Ensure proper reporting and follow-up of SAEs, address non-compliance issues, and assist with audit/inspection readiness.

Premier Research is a global clinical research, product development, and consulting company helping biotech, specialty pharma, and MedTech innovators turn breakthroughs into new treatments. The company fosters a collaborative culture focused on agility, continuous learning, and making an impact.

• Lead operational delivery of Phase I clinical studies from start-up through close-out as the day-to-day counterpart to the CRO.
• Own site relationships, drive activation readiness, and manage recruitment performance for complex dose-escalation studies.
• Ensure quality and timeliness of clinical data, supplies, and vendor deliverables while maintaining ICH GCP compliance.

Numab Therapeutics is a Swiss biotech developing multi-specific antibody immunotherapies. It has a broad pipeline and completed a major J&J transaction, with Series C funding of CHF 180 million.

• Monitor clinical studies at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP.
• Coordinate study setup and initiation activities, including investigator identification and regulatory submissions.
• Identify study risks and propose mitigation strategies while maintaining high quality and detail.

Precision for Medicine is a CRO integrating clinical trial execution with scientific expertise and data sciences, focusing on Oncology and Rare Disease. It offers a supportive, small-CRO culture with high CRA retention and emphasis on work-life balance.

• Oversee GCP compliance, manage deviations and CAPAs, and conduct quality and TMF reviews.
• Maintain inspection readiness and support CRO oversight per ICH E6(R3).
• Collaborate with Data and Clinical teams to embed compliance into workflows and train teams.

Resilience Care is a French medtech founded in 2021, offering AI remote monitoring for oncology, gastroenterology, and psychiatry. It serves 35,000 patients across 200+ facilities with an agile, collaborative culture.

• Serve as primary point-of-contact liaison with clients and oversee all aspects of clinical trials.
• Manage study budgets, project timelines, risk, and cross-functional teams to ensure quality and compliance.
• Drive bid defense preparation, client presentations, and continuous process improvement across assigned portfolios.

Precision for Medicine supports clinical research and development for biopharmaceutical and life science companies. It is a global, collaborative organization that emphasizes quality, innovation, and professional growth.

• Collaborate with project teams to support study startup and serve as primary point of contact for clinical sites.
• Provide training on Beacon's devices and protocols, monitor progress, and maintain GCP/ICH compliance.
• Address operational issues via Zendesk and Asana and deliver actionable site feedback for workflow improvements.

Beacon Biosignals is transforming precision medicine for the brain with at-home EEG and cardiopulmonary monitoring platforms for clinical development and diagnostics. They foster a remote-first culture with hubs in Boston, New York, and Paris, emphasizing curiosity, simplicity, and empathy.