Project Program Manager Jobs at Syneos Health with Visa Sponsorship
Project Program Manager jobs at Syneos Health sit at the intersection of clinical operations and strategic delivery, requiring you to coordinate complex research programs across global teams. Syneos Health has an established track record of sponsoring work visas for this function, making it a realistic target if you need employer support.
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Get Access To All JobsINTRODUCTION
Clinical Project Manager II – Biomarker Study Management Experience required (Sponsor Dedicated - US Remote; Preference for Hybrid Foster City, CA)
Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.
Our Clinical Solutions team members act with a drug development mindset, 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 achieve 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 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 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 all want to work for and our customers want to work with. Why? Because we know that when 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 progress.
Job Responsibilities
Clinical Project Manager II – Biomarker Study Management
Sponsor-Dedicated | Remote
(Preference for Hybrid Foster City, CA-Based Candidates)
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.
While remote/home-based candidates may be considered, priority will be given to candidates located within 50 miles Foster City, California, with the ability to work onsite 2–3 days per week.
WHAT YOU WILL 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 needed
Candidates without direct experience supporting Biomarker clinical trials can not be considered.
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.
- 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 with your expertise, 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 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 all applicable federal, state, and municipal paid sick time requirements.
Salary Range:
$95,000.00 - $175,700.00
The base salary range represents the anticipated low and high of the Syneos Health 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 Syneos Health
Over the past 5 years, we have worked with 94% of all 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 quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.
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 comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
INTRODUCTION
Clinical Project Manager II – Biomarker Study Management Experience required (Sponsor Dedicated - US Remote; Preference for Hybrid Foster City, CA)
Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.
Our Clinical Solutions team members act with a drug development mindset, 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 achieve 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 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 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 all want to work for and our customers want to work with. Why? Because we know that when 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 progress.
Job Responsibilities
Clinical Project Manager II – Biomarker Study Management
Sponsor-Dedicated | Remote
(Preference for Hybrid Foster City, CA-Based Candidates)
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.
While remote/home-based candidates may be considered, priority will be given to candidates located within 50 miles Foster City, California, with the ability to work onsite 2–3 days per week.
WHAT YOU WILL 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 needed
Candidates without direct experience supporting Biomarker clinical trials can not be considered.
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.
- 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 with your expertise, 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 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 all applicable federal, state, and municipal paid sick time requirements.
Salary Range:
$95,000.00 - $175,700.00
The base salary range represents the anticipated low and high of the Syneos Health 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 Syneos Health
Over the past 5 years, we have worked with 94% of all 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 quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.
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 comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
See all Project Program Manager Jobs at Syneos Health
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Project Program Manager Jobs at Syneos Health.
Get Access To All JobsTips for Finding Project Program Manager Jobs at Syneos Health
Align your PMP credentials before applying
Syneos Health's Project Program Manager roles consistently require demonstrated program governance experience in clinical or life sciences settings. A PMP certification paired with CRO or pharma delivery experience positions your application as a stronger sponsorship candidate from the start.
Target roles listed under clinical operations
Syneos Health posts Project Program Manager openings across multiple business units. Filtering by clinical operations or functional service provider divisions surfaces the roles most likely to carry sponsorship budget, since those units handle ongoing sponsor-facing program delivery.
Confirm LCA filing before accepting an offer
Before your H-1B petition moves to USCIS, your employer files a Labor Condition Application with the DOL certifying your prevailing wage. Ask your Syneos Health recruiter where that process stands so you understand the timeline before you give notice to a current employer.
Use Migrate Mate to filter open roles by visa type
Syneos Health's sponsorship history varies by role and business unit. Use Migrate Mate to browse current Project Program Manager openings filtered by visa type, so you spend time only on positions where H-1B or OPT sponsorship has been documented.
Prepare to address your nonimmigrant intent clearly
F-1 OPT and TN visa holders applying to Syneos Health should be ready to walk hiring managers through their current work authorization status and expiry dates. Recruiters in life sciences program management are generally familiar with OPT cap-gap, but having a clear timeline ready removes friction.
Sequence your PERM timeline around project milestones
If Syneos Health agrees to sponsor a Green Card through EB-2 or EB-3, PERM labor certification typically takes 12 to 18 months before the I-140 stage. Raise the conversation during your offer negotiation, not after onboarding, so your priority date starts accruing as early as possible.
Frequently Asked Questions
Does Syneos Health sponsor H-1B visas for Project Program Managers?
Yes, Syneos Health sponsors H-1B visas for Project Program Manager positions. Sponsorship is most common in clinical operations and program delivery functions, where specialized life sciences experience supports the specialty occupation standard USCIS requires. If you're on F-1 OPT, Syneos Health has also sponsored transitions from OPT to H-1B visa for this role type, though availability depends on the specific business unit hiring.
How do I apply for Project Program Manager jobs at Syneos Health?
Applications go through Syneos Health's careers portal, where you can filter by job function and location. When applying, clearly indicate your visa status and authorization needs in your cover materials, since recruiters in life sciences program management are accustomed to assessing sponsorship eligibility early. Migrate Mate also lists Syneos Health's open Project Program Manager roles filtered by sponsorship type, which helps you identify the right postings faster.
Which visa types does Syneos Health commonly use for Project Program Manager roles?
Syneos Health has sponsored H-1B visas as the primary work authorization pathway for Project Program Managers, with Green Card sponsorship available through EB-2 or EB-3 for longer-tenured employees. F-1 OPT is accepted during the initial hiring stage, and TN visa holders in qualifying professional categories may also be eligible. The specific pathway offered depends on your nationality, degree field, and the hiring team's budget.
What qualifications does Syneos Health expect for Project Program Manager roles?
Syneos Health typically requires a bachelor's degree in a life sciences, business, or related field, combined with several years of program or project management experience in a clinical research organization or pharmaceutical environment. PMP certification strengthens your candidacy. Roles often involve managing cross-functional teams across clinical trial phases, so experience with ICH-GCP guidelines or clinical operations workflows is a practical differentiator beyond the baseline degree requirement.
How long does the visa sponsorship process take for Syneos Health hires?
For H-1B sponsorship, Syneos Health must first file a Labor Condition Application with the DOL, which typically takes one to two weeks when processed electronically. The USCIS H-1B petition then takes three to six months under standard processing, or two to four weeks with premium processing. If you're cap-subject, your start date cannot precede October 1 of the fiscal year your petition was selected in, so plan your offer timeline around that constraint.