Manage and oversee all clinical aspects of trials across multiple countries, ensuring timeline adherence, quality, and scope.
Lead CRAs and collaborate with cross-functional teams to achieve high client satisfaction and smooth trial operations.
Identify risks, develop creative action plans, and maintain focus on study priorities through effective communication.
Precision for Medicine is a precision medicine CRO that combines novel trial designs, advanced biomarker analytics, and deep oncology expertise to accelerate drug development. The company fosters a dynamic, high-energy culture and values dedicated professionals who thrive in challenging environments.
Lead the delivery of complex global projects for clients within the contract research, life sciences, or regulated healthcare sectors.
Manage the full project lifecycle, including planning, execution, monitoring, reporting, delivery, and closure.
Coordinate cross-functional international teams and develop project plans, timelines, budgets, and resource allocation strategies.
Welo Life Sciences is a specialized language and technology partner serving pharmaceutical, CRO, and medical device organizations in regulated global markets. It is a part of Welo Global brand, delivering solutions within a secure, audit-ready framework supported by seven ISO certifications.
Direct and manage a team of Project Directors and Project Managers in global clinical program planning and execution.
Interact with study sponsors as the primary escalation point and optimize profitability of the Project Management organization.
Select, train, develop, and manage talent in project leadership roles, ensuring compliance with SOPs and regulatory requirements.
Precision Medicine Group is a life science company that provides clinical research, data analytics, and commercial services to biopharmaceutical clients. They are a sizeable organization with a focus on quality, people, clients, and performance, fostering a culture of collaboration and continuous improvement.
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.
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.
Review, draft, negotiate, and track legal agreements including confidentiality agreements, clinical study agreements, and amendment agreements across APAC.
Set up contracting strategies for assigned projects and work closely with Clinical Operations study team to ensure deliverables align with study timelines.
Be fully responsible for Site Contract Management from setting up site contracting strategy to execution of contracts, including budget negotiations with sites.
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. They have brought together new technologies, expertise, and operational scale to help the life sciences industry.
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.
Lead project teams through discovery, design, build, and configuration for healthcare and life sciences customers.
Manage day-to-day project operations, timelines, budget, and scope, ensuring on-time and on-budget delivery.
Proactively identify and manage project risks, building risk mitigation plans and escalating issues as needed.
Komodo Health reduces the global burden of disease by building the Healthcare Map, the industry's largest, most complete view of the U.S. healthcare system. They are a team of ambitious Dragons with diverse backgrounds, focused on data-driven healthcare solutions.
Direct strategic change projects across Global Clinical Trial Operations (GCTO) to ensure on-time, high-quality delivery.
Drive cross-initiative change management efforts, including liaising with change agent networks and aligning training plans.
Establish process standards and promote best practices for how teams approach projects and initiatives.
Merck & Co., Inc. is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.
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.