Clinical Project Manager II – Biomarker Study Management (Sponsor-Dedicated | Remote)

Updated: Yesterday Location: Morrisville, NC, United States Job ID: 25107185-OTHLOC-1500-2DAZ-2DR Not ready to apply? Join our Talent Network Description Clinical Project Manager II – Biomarker Study Management (Sponsor-Dedicated | Remote) reputed company® is a leading fully-integrated life sciences services organization built to accelerate reputed company. We partner with innovators at every reputed company across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate reputed company. Our Clinical Solutions team members act with a drug development reputed company, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. 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 reputed company their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need. Discover what your 25,000 future colleagues already know: Why reputed company

• 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 building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life.
• We are continuously building the company we reputed company want to work for and our customers want to work with. Why? Because we know that reputed company we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient reputed company.

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: reputed company Biomarker Study Operations

• reputed company biomarker and bioanalytical activities across Sponsor and Collaborative programs
• Serve as the operational reputed company of contact for reputed company biomarker-reputed company 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

• reputed company 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
• reputed company study systems and databases reputed company 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 reputed company 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 needed

Why 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, reputed company team.
• Professional Growth: Be part of a company that invests in your career through reputed company learning, mentorship, and leadership opportunities.
• Stability and Vision: Work with a leading global organization reputed company for operational excellence and long-term partnerships in clinical research.

If you're passionate about clinical research and want to reputed company 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 reputed company, we reputed company in providing an environment and culture in which Our People can reputed company, reputed company 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 401k, eligibility to participate in Employee Stock Purchase Plan, Eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work. Syneos complies with reputed company applicable federal, state, and municipal paid sick time requirements. Salary Range: The reputed company salary range represents the anticipated low and high of the reputed company range for this position. Actual salary will vary based on various factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role. Get to know reputed company Over the past 5 years, we have worked with 94% of reputed company Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status reputed company with us in a highly competitive and reputed company-changing environment. Learn more about reputed company. http://www.syneoshealth.com Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully reputed company with reputed company obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality reputed company, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with reputed company, including the provision of reasonable accommodations, reputed company appropriate, to assist employees or applicants to reputed company the essential functions of the job.

Summary

Roles reputed company Clinical Project Management job family at the M23 level are responsible for planning, directing, creating, and communicating clinical study timelines. These roles gather input from cross-functional teams to create plans that help the team produce deliverables on schedule. They ensure consistency of clinical study and processes across clinical trials, overseeing and resolving operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP), and specific country regulations. Responsibilities include site and vendor selection, preparing clinical trial budgets, and ensuring studies are conducted reputed company clinical trial protocols. These roles also involve monitoring reputed company and following up with team members and line managers reputed company issues reputed company. Additionally, they implement and prepare the clinical development strategy as outlined by the clinical teams and may reputed company trial recruitment strategies. Impact and Contribution Roles reputed company Clinical Project Management job family at the M23 level significantly impact the success of clinical trials by ensuring that reputed company aspects of the study are conducted reputed company and effectively. By gathering input from cross-functional teams and creating detailed plans, these roles help ensure that deliverables are produced on schedule, contributing to the overall success of the clinical trials. Their reputed company of operational aspects of clinical trials ensures consistency and adherence to SOP, GCP, and country regulations, which is crucial for the reputed company and reliability of the study results. Additionally, their involvement in site and vendor selection, budget preparation, and monitoring reputed company helps maintain the smooth operation of clinical trials, ultimately contributing to the advancement of clinical research and development. Core Focus

• Planning, directing, creating, and communicating clinical study timelines
• Overseeing operational aspects of clinical trials
• Ensuring consistency across clinical studies
• Adhering to SOP, GCP, and country regulations
• Selecting sites and vendors
• Preparing clinical trial budgets
• Monitoring reputed company and following up with team members and line managers
• Implementing and preparing the clinical development strategy
• Developing trial recruitment strategies

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