Source Job

• Accountable for leading assigned clinical research activities and partnering with stakeholders on study design.
• Conducts on-site and remote site visits, including qualification, initiation, monitoring, and close-out.
• Tracks study progress, manages budgets, and mentors junior clinical study managers.

Intuitive is a pioneer and market leader in robotic-assisted surgery, dedicated to minimally invasive care. With over 25 years of experience, the company fosters an inclusive and diverse team culture where employees are empowered to do their best work.

• Design and execute IRB protocols, managing consent and patient enrollment for high-priority clinical studies.
• Build cross-functional research infrastructure with Clinical Operations, Product, and Data teams.
• Draft white papers, conference abstracts, and contribute to peer-reviewed publications.

Nourish is building the largest dietitian-led metabolic health clinic, offering AI-native digital health services across all 50 states. Founded four years ago, the company has completed millions of appointments, tripled year-over-year, and raised $215M in funding, partnering with health plans covering over 200M Americans.

• Establish and execute the clinical research and publication strategy at Headway.
• Own end-to-end planning of the research roadmap in conjunction with Clinical Leadership.
• Lead projects from conceptualization to execution, driving deep analytical insight through strategic analysis and experimentation.

Headway builds a new mental healthcare system by automating insurance admin for therapists. With over 75,000 providers and $325M+ in funding from top VCs, they are a Series D company scaling the platform where care happens.

• Provides study-level oversight and leadership for global clinical trials from inception through closure, managing vendors, recruitment, and cross-functional teams.
• Develops and manages study materials including protocols, regulatory submissions, and budgets while ensuring compliance with quality standards and inspection readiness.
• Contributes to system management like EDC, IRT, and eTMF, and supports process improvement initiatives or serves as a mentor.

AbbVie discovers and delivers innovative medicines and solutions to address serious health issues in immunology, oncology, neuroscience, and aesthetics. As a global biopharmaceutical company with a robust pipeline, they emphasize integrity and innovation, serving patients worldwide with a dedicated team.

• Lead and nurture a team of experienced clinical researchers conducting virtual trials and publishing peer-reviewed data.
• Build a network of key investigators and develop a real-world evidence program using claims and clinical datasets.
• Partner with Commercial Marketing and Sales to translate clinical outcomes into a compelling market narrative.

Virta Health reverses metabolic disease in one billion people through technology, personalized nutrition, and virtual care. They have raised over $350 million and partner with health plans, employers, and government organizations.

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
• Collaborating with investigators and site staff to facilitate smooth study conduct.

ICON is a global healthcare intelligence and clinical research organization dedicated to accelerating the development of new medicines and treatments. As a values-driven company, ICON fosters a culture of integrity, collaboration, agility, and inclusion, employing a diverse workforce.

• Lead the design, execution, and oversight of HEOR and RWE studies including observational studies and economic models.
• Develop and execute integrated HEOR strategies aligned with product development and market access needs.
• Oversee vendor selection, manage timelines and budgets, and ensure compliance with regulatory standards.

Mineralys Therapeutics is a clinical-stage biopharmaceutical company focused on developing medicines for hypertension and related diseases. The company is headquartered in Radnor, Pennsylvania and operates as a fully remote organization.

• Independently prepare IRB documents, maintain regulatory files, and facilitate regulatory oversight of safety reporting for clinical trials.
• Serve as the internal project manager for assigned oncology disease groups, providing timely updates and regulatory guidance.
• Manage study activation processes and act as liaison between sponsors, investigators, and internal departments.

Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate today and prepare leaders for the future. Winship Cancer Institute is Georgia's only NCI-designated Comprehensive Cancer Center, dedicated to discovering cures for cancer and providing innovative therapies.

• Conduct literature reviews to develop and refine metrics for medical conditions and procedures.
• Create and validate measures using proprietary technical and statistical tools.
• Collaborate with product, data science, and engineering teams to support new product development.

Garner transforms the healthcare economy by partnering with employers to redesign healthcare benefits using data-driven insights. As one of the fastest-growing healthcare technology companies in the US, they build a team of mission-driven individuals committed to making a meaningful impact on healthcare at scale.

• Serve as the primary point of contact and partner with investigative sites to ensure high-quality clinical trial conduct.
• Conduct site evaluation, training, monitoring, and closure activities in compliance with regulations, GCPs, and SOPs.
• Utilize risk-based monitoring and site engagement strategies to improve data integrity, compliance, and study performance.

AbbVie discovers and delivers innovative medicines and solutions across immunology, oncology, neuroscience, and aesthetics. A large global biopharmaceutical company, AbbVie fosters a culture of innovation and integrity to transform patients' lives.

• Manage a team of 15-17 Study Management Associates (SMAs) to deliver best-in-class study execution.
• Drive performance management, mentoring, and professional development for direct reports.
• Support resource management, adherence to regulations, and continuous process improvements.

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. The company operates across several therapeutic areas including immunology, oncology, and neuroscience, with a significant global presence and a culture focused on innovation and impact.

• Lead Omada's Clinical Quality department with end-to-end accountability for program integrity, performance, and continuous improvement across cardiometabolic programs.
• Define and drive the near-term roadmap for program quality, accreditation readiness, quality analytics, and AI bias monitoring.
• Build durable quality infrastructure that supports a growing portfolio of clinical products and care experiences, partnering across teams.

Omada Health is a virtual-first healthcare company on a mission to bend the curve of chronic disease by combining human-led care teams, connected devices, and AI-enabled technology. The company has served over two million members across 2,000+ employers and health plans, and fosters a culture of trust, context, boldness, and collaboration.

• Conduct qualification, initiation, interim, and close-out monitoring visits (on-site and remote) in compliance with GCP, ICH, and SOPs.
• Build and maintain strong relationships with investigator sites, providing training and guidance to ensure study quality.
• Support IRB submissions, regulatory documentation, and trial master file quality across clinical programs.

CoMind develops non-invasive neuromonitoring technology for clinical brain monitoring. The company is a cutting-edge startup focused on improving diagnosis and treatment of brain disorders, with a culture that embraces AI in daily work.

• Design and execute clinical outcomes research initiatives to evaluate treatment effectiveness.
• Manage and analyze large clinical datasets using statistical methodologies to support data-driven decision-making.
• Collaborate cross-functionally with clinical, operations, and product teams to drive quality improvement and evidence-based care.

InStride Health delivers specialty anxiety and OCD care for children and families, combining research-backed clinical care with innovative technology. As a mission-driven, fully remote team, they prioritize diversity, equity, and inclusion, and are expanding access to insurance-based mental health treatment.

• Build trust and credibility for Oura among members, physicians, scientists, and health systems.
• Collaborate with engineering, product, design, data science, and algorithm teams to define clinical features for metabolic health.
• Design and oversee clinical validation studies to demonstrate product performance and relevance in the metabolic space.

Oura empowers individuals to own their inner potential with award-winning products that provide insights into readiness, activity, and sleep quality. As a quickly growing company focused on health, they ensure team members have what they need to do their best work.

• Act as primary clinical point of contact with clients and lead planning, execution, and oversight of clinical studies across Latin America.
• Develop country-level recruitment strategies, guide monitoring and quality strategies, and mentor CRAs and partners.
• Collaborate with project managers on budgets, vendor management, and ensure compliance with ICH-GCP and regulatory requirements.

Precision Medicine Group is a precision medicine company that provides clinical research and commercialization services. The company is an Equal Opportunity Employer with a focus on expanding clinical operations across Latin America.

• Manage all aspects of clinical trials from start-up through close-out, ensuring timelines, costs, and quality metrics are met.
• Oversee vendor/CRO selection and management, study contracting, budgeting, and forecasting.
• Lead study-related activities including protocol preparation, investigator selection, and training, and collaborate with cross-functional teams.

Natera is a global leader in cell-free DNA testing, dedicated to oncology, women’s health, and organ health. The team consists of highly dedicated professionals from world-class institutions who care deeply for their work and each other.

• Serves as clinical trial lead, overseeing study planning, conduct, and oversight per protocol and regulations.
• Develops study documents, manages site feasibility, and drives recruitment strategies.
• Leads internal clinical team meetings and ensures quality deliverables through metric reporting.

Precision Medicine Group is a life sciences company that supports clinical research and development. The company is large enough to offer a range of benefits and emphasizes a collaborative, ethical culture focused on quality and compliance.

• You will monitor and own the progress of clinical studies at investigative sites, ensuring compliance with protocols, SOPs, ICH-GCP, and regulations.
• You will coordinate all activities to set up and monitor a study, including identifying investigators and preparing regulatory submissions.
• You will travel domestically up to 50-60% for site visits and maintain fluency in English and local language.

Precision for Medicine is a clinical research organization focused on precision medicine for oncology and rare diseases. They are a smaller CRO with a strong culture and high employee retention.

• Responsible for site activation readiness, including preparation and submission of Clinical Trial Application Forms to Competent Authorities and Ethics Committees.
• Manage collection of essential documents, customize informed consent forms, and coordinate translations for study-specific documents.
• Maintain communication with key functions (Feasibility, Clinical Operations, Regulatory) and update project trackers and regulatory intelligence tools.

Precision for Medicine is a Clinical Research Organization focused on precision medicine, combining novel clinical trial designs and advanced biomarker solutions, particularly in rare diseases and oncology. The company is growing and seeks dedicated professionals to support its mission, fostering a culture where employees feel appreciated and their ideas valued.