Project Manager II - Inflammation/ Phase 2b (Sponsor Dedicated - Remote; Preference for Hybrid Foster City, CA)

Project Manager II - Inflammation/ Phase 2b (Sponsor Dedicated - 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 – Inflammation

Sponsor-Dedicated | Remote (U.S.)
Preference for Hybrid Foster City, CA-Based Candidates

Are you a clinical project management professional who knows how to take ownership of a study from start-up through closeout — not just oversee it from a distance, but truly drive execution day-to-day?

This is a highly visible opportunity supporting a complex Phase 2b inflammation program within a fast-paced sponsor-dedicated environment where strong operational leadership, accountability, and execution matter. The ideal candidate is comfortable operating both strategically and tactically — someone who can lead cross-functional teams while also rolling up their sleeves and working in the details to keep a study moving forward.

If you thrive in high-accountability environments, can navigate ambiguity, and enjoy being deeply involved in clinical trial execution from start to finish, this role offers the opportunity to make a direct impact.

While remote/home-based candidates may be considered, priority will be given to candidates located in or near Foster City, California, with the ability to work onsite 2–3 days per week.

WHY THIS OPPORTUNITY

• High-impact role supporting a complex Phase 2b inflammation study

• Opportunity to lead regional execution efforts within a large global clinical program

• Strong visibility across Clinical Operations, leadership, and external partners

• Fast-moving environment where decisions and execution happen quickly

• Significant ownership and autonomy with the expectation to independently drive study progress

• Collaborative sponsor-dedicated culture with supportive leadership and strong team partnership

• Opportunity to work alongside highly experienced clinical operations professionals in a hands-on environment

WHAT YOU WILL OWN

End-to-End Clinical Trial Execution

• Drive operational execution of a complex Phase 2b inflammation study from study start-up through database lock and closeout

• Independently manage day-to-day study operations with minimal oversight

• Own timelines, deliverables, risks, and issue resolution across multiple workstreams

• Maintain deep operational awareness across all aspects of the trial — this is a role for someone comfortable working “in the weeds”

• Ensure study milestones stay on track in a fast-paced environment with shifting priorities and competing demands

• Partner cross-functionally to proactively identify risks, remove roadblocks, and implement operational solutions quickly

Vendor & CRO Oversight

• Lead vendor management activities and maintain strong oversight of external partners and CROs

• Contribute to RFP development, vendor selection, and ongoing vendor performance management

• Hold vendors accountable to timelines, deliverables, quality expectations, and issue resolution

• Actively manage operational follow-through rather than relying solely on escalation pathways

Cross-Functional Leadership

• Lead cross-functional meetings with clear agendas, action-oriented discussions, and strong follow-up

• Drive accountability across internal teams and external partners

• Build strong collaborative relationships while effectively navigating challenging conversations and competing priorities

• Mentor or support junior team members as needed

• Operate confidently within a matrixed global environment with multiple stakeholders

Study Operations & Documentation

• Draft, review, and coordinate key study documents including protocols, informed consents, monitoring plans, investigator brochures, and clinical study reports

• Support study budget tracking, forecasting, and operational planning activities

• Review data listings and support interim/final reporting activities

• Train CROs, investigators, study coordinators, and vendors on protocol and study requirements

• Contribute to SOP development, process improvement initiatives, and operational best practices

WHAT YOU BRING

Required Experience

• 3+ years of clinical project management experience within clinical research

• Experience running clinical trials from start-up through closeout, with a strong understanding of the full clinical trial lifecycle

• Experience supporting complex Phase 2b studies within the inflammation therapeutic area

• Strong CRO/vendor management and oversight experience

• Proven ability to independently drive study execution in fast-paced clinical environments

• Experience managing cross-functional clinical trial activities within matrixed organizations

• Comfortable balancing strategic oversight with hands-on operational execution

Key Strengths

• Highly organized with exceptional follow-through and attention to operational detail

• Comfortable working in the weeds while still maintaining a high-level program perspective

• Ability to prioritize effectively and pivot quickly in fast-moving environments

• Strong meeting leadership, communication, and stakeholder management skills

• Confident driving accountability across teams and vendors

• Solutions-oriented mindset with strong initiative and urgency

• High emotional intelligence and ability to navigate high-stakes conversations professionally

• Collaborative, transparent, and team-oriented approach

Technical & Regulatory Expertise

• Thorough knowledge of FDA and EMA regulations, ICH Guidelines, and GCP requirements

• Strong working knowledge of Microsoft Word, Excel, and PowerPoint

• Ability to interpret and explain protocol requirements, operational processes, and study expectations to teams and stakeholders

TEAM CULTURE

This team values collaboration, accountability, and execution. The environment is fast-paced, highly interactive, and best suited for individuals who enjoy being actively engaged in study operations rather than operating at a distance. Leadership is approachable, mentorship-focused, and supportive, while still maintaining high expectations around ownership and delivery.

The team works hard, communicates openly, and genuinely supports one another to keep studies moving forward successfully.

If you are looking for an opportunity where you can independently lead a complex clinical trial from start to finish, operate in a fast-paced environment, and play a hands-on role in execution and delivery, this is an excellent next step in your clinical operations career.

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.

Summary

Roles within Clinical Project Management job family are responsible for planning, directing, creating and communicating clinical study time-lines. Gathers input from cross-functional teams and creates plans that help the team produce deliverables on schedule. Ensures 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 such as site and vendor selection, preparing clinical trial budgets. Ensures studies are conducted within clinical trial protocols, monitoring progress and following up with team members and line managers when issues develop. Implements and prepares the clinical development strategy as outlined by the clinical teams. May develop trial recruitment strategies. Impact and Contribution Includes executives as well as managers, supervisors and team leads providing strategic vision and/or tactical direction across a discipline and/or broader organization. The majority of time is spent overseeing their area of responsibility, planning, prioritizing, and/or directing the responsibilities of employees. Goal are achieved through management of process, policy, and performance of direct and/or indirect reports. Supervises experienced support employees and/or entry individual contributors. Delivers operational results that have moderate impact on the immediate achievement of results for the team. Broad job knowledge in an operational, administrative and/or specialized field, adapts new procedures, techniques, tools, etc. Understands basic management approaches such as work scheduling, prioritizing, coaching and process execution.