Project Manager II
- Inflammation/ Phase 2b (Sponsor-Dedicated /Remote
- U.S.) サイネオス・ヘルス Morrisville, NC Job Details $95,000
- $175,700 a year 21 hours ago Benefits Employee stock purchase plan Company car Health insurance Dental insurance Paid time off Vision insurance 401(k) matching Paid sick time Qualifications Clinical research Vendor relationship management Cross-functional collaboration Cross-functional team management
Full Job Description Updated:
Today Location:
Morrisville, NC, United States Job ID:
25108333-OTHLOC-1500-2DMI-2DR Not ready to apply? Join our Talent Network Description Project Manager II
- Inflammation/ Phase 2b (Sponsor-Dedicated /Remote
- U.
S.) 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 Project Manager II
- Inflammation Sponsor-Dedicated | Remote (U.
S.) If you are an experienced clinical project management professional who thrives in complex, fast-moving studies and enjoys leading cross-functional teams with confidence and precision, this is an opportunity to step into a highly visible role supporting a complex Phase 2b inflammation program within a sponsor-dedicated environment. This role is ideal for someone who brings strong vendor oversight experience, operational leadership, and the ability to independently drive study execution while navigating a matrixed, high-accountability clinical environment. Why This Opportunity High-impact role supporting a complex Phase 2b inflammation study Opportunity to lead regional execution efforts within a large, cross-functional global program Strong visibility across Clinical Operations and external partners Collaborative sponsor-dedicated environment with a highly supportive leadership team Manager who believes in mentorship, teamwork, and professional growth Team culture centered around partnership, accountability, and mutual support What You'll Own Clinical Trial Leadership & Execution Manage regional components of a large, complex clinical trial within the inflammation therapeutic area Independently drive study activities with minimal oversight Lead cross-functional timelines and ensure alignment across stakeholders Proactively identify operational risks, escalate issues appropriately, and implement solutions Support study logistics and operational planning to achieve program milestones Vendor & Service Provider Oversight Lead vendor management activities and maintain strong oversight of external partners Contribute to RFP development and participate in CRO/service provider selection processes Ensure accountability across vendors while maintaining productive working relationships Support operational issue resolution and follow-through on deliverables Cross-Functional Leadership Lead meetings effectively by setting agendas, facilitating productive discussions, documenting decisions, and driving action items to completion Partner across Clinical Operations and study teams to maintain executional excellence Provide leadership and mentorship to junior team members when needed Foster collaboration and accountability across internal and external stakeholders Study Management & Operations Draft and coordinate review of key study documents including protocols, informed consents, monitoring plans, investigator brochures, and clinical study reports Maintain study timelines and support study budget activities Coordinate review of data listings and support interim/final clinical study reporting activities Train CROs, investigators, study coordinators, and service providers on study requirements as needed 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 supporting complex Phase 2b clinical studies within the inflammation therapeutic area Strong vendor management and oversight experience Demonstrated understanding of the full clinical trial lifecycle from start-up through closeout Experience managing cross-functional clinical trial activities in a matrixed environment Ability to independently manage priorities and navigate operational challenges with minimal supervision Key Strengths Strong meeting leadership and communication skills High emotional intelligence with the ability to communicate tactfully in high-stakes discussions Confident leading cross-functional teams and driving accountability Excellent organizational, decision-making, and problem-solving abilities Positive, solutions-oriented mindset with strong initiative Collaborative approach with a focus on transparency and teamwork Technical & Regulatory Expertise Thorough knowledge of FDA and EMA regulations, ICH Guidelines, and GCP requirements Strong working knowledge of Word, Excel, and PowerPoint Ability to understand, interpret, and explain protocol requirements to study teams and stakeholders Team Culture This team values collaboration over silos and believes the best outcomes happen when people genuinely support one another. The leadership style is mentorship-focused, approachable, and highly team-oriented. Peers are motivating, encouraging, and dependable—creating an environment where accountability and partnership go hand in hand. If you are looking for an opportunity where you can operate independently, lead complex clinical trial activities, and make a direct impact within a collaborative sponsor environment, this is a strong next step in your 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
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.
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 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.
