Clinical Project Manager II - Biomarker Study Management (Sponsor-Dedicated | Remote)
Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.
Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.
Discover what our 29,000 employees, across 110 countries already know:
WORK HERE MATTERS EVERYWHERE
Why Syneos Health
We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
We are committed to our Total Self culture - where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives - we're able to create a place where everyone feels like they belong.
Job Responsibilities
Clinical Project Manager II - Biomarker Study Management(Sponsor-Dedicated | Remote)
We're hiring a Clinical Project Manager II with a strong background in biomarker study operations to join our sponsor-dedicated team. This fully remote role gives you the opportunity to drive the success of global clinical trials by leading biomarker and bioanalytical strategy from start to finish.
You'll be a key player in bringing together cross-functional teams, vendors, and internal stakeholders to ensure biological samples are collected, managed, and analyzed to the highest standards.
What You'll Do:
Lead Biomarker Study Operations
Oversee biomarker and bioanalytical activities across Sponsor and Collaborative programs
Serve as the operational point of contact for all biomarker-related processes
Work closely with clinical study teams (Phases 1-4) to integrate biomarker strategies into broader clinical development plans
Plan and manage the collection, tracking, and analysis of biological specimens
Advise study teams on best practices for sample management and logistics
Drive Clinical Project Delivery
Lead cross-functional teams through the full clinical trial lifecycle, from start-up to closeout
Ensure studies stay on track with respect to timelines, budget, scope, and quality
Act as the main liaison between the sponsor and study partners
Monitor and manage project financials, ensuring fiscal responsibility
Proactively identify and resolve operational issues and risks
Ensure Operational Excellence
Maintain high-quality documentation, including Trial Master File (TMF) accuracy and completeness
Keep study systems and databases current and audit-ready
Prepare project reports and updates for sponsors and internal stakeholders
Plan and facilitate internal and external meetings
Support inspection readiness and regulatory compliance throughout the project
Skills and Experience You Bring:
Significant experience managing biomarker studies and external vendors required!
Strong understanding of biomarker and bioanalytical strategies in a clinical trial setting
Proven ability to coordinate complex sample collection and analysis workflows
Expertise in supporting study teams with sample logistics and operational planning
Bachelor's degree in Life Sciences, Medicine, Pharmacy, Nursing, or equivalent combination of education and experience
Experience in a clinical research organization (CRO) or sponsor environment preferred
Familiarity with GCP, ICH guidelines, and global regulatory standards
Strong project management, organizational, and communication skills
Comfortable working independently and embracing new technologies
Willingness to travel up to 25% as neededWhy Join Us:
Meaningful Work: Your contributions will directly support critical biomarker research that shapes the future of clinical development and precision medicine.
Global Impact: You'll be working on high-profile studies that span multiple regions, making a real difference in patients' lives around the world.
Dedicated Team: Join a collaborative, sponsor-dedicated environment where your expertise is trusted, and your voice matters.
Flexibility: Enjoy the freedom of a fully remote role with the support of a structured, responsive team.
Professional Growth: Be part of a company that invests in your career through continued learning, mentorship, and leadership opportunities.
Stability and Vision: Work with a leading global organization known for operational excellence and long-term partnerships in clinical research.
If you're passionate about clinical research and want to make a direct impact on advancing biomarker science, we'd love to hear from you.
Apply now and be part of a team shaping the future of clinical development.
At Syneos Health, we believe in providing an environment and culture in which Our People can thrive, develop and advance. We reward and recognize our people by providing valuable benefits and a quality-of-life balance. The benefits for this position may include a company car or car allowance, Health benefits to include Medical, Dental and Vision, Company match... For full info follow application link.
