Project Manager - Sponsor Dedicated (Inflammation)

Syneos Health Careers$100K — $120K *
US-AnywhereRemote in North Carolina, US
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • 5-7 years of experience in clinical project management
  • Extensive knowledge of clinical trial methodology
  • Experience specifically in inflammation studies
  • Strong leadership skills in managing clinical teams
  • Proven global clinical trial experience
  • Ability to manage project timelines and budgets
  • Excellent communication skills in interpersonal and written forms

Responsibilities

  • Guide and oversee all aspects of international clinical trials
  • Communicate project status with functional peers and ensure goals are met
  • Oversee operational details of assigned trials, including start-up and close-out
  • Prepare and develop study-related documents and plans
  • Coordinate data review for analysis purposes
  • Participate in developing study strategies and budgets
  • Manage CRO interactions and operational oversight for studies

Benefits

  • Company car or car allowance
  • Health benefits including medical, dental, and vision
  • 401k plan with company match
  • Eligibility for Employee Stock Purchase Plan
  • Opportunities for performance-based commissions and bonuses
  • Flexible paid time off (PTO) and sick time
Full Job Description
Project Manager - Sponsor Dedicated (Inflammation)

Job Responsibilities

Sr. Project Manager - Sponsor Dedicated (Inflammation)

Location: Remote, USA

Role Summary:

We are seeking a skilled and motivated Sr. Project Manager to join our sponsor-dedicated team supporting high-impact inflammation trials. In this role, you will work full-time on behalf of a leading biopharmaceutical sponsor while employed within a global CRO-offering the best of both worlds: sponsor collaboration and CRO resources.

What You Will Do:
  • In partnership with Clinical Program Manager or Associate Director, provides guidance and daily oversight for the successful management of all aspects of international clinical trials within designated program budgets and timelines
  • Communicates with functional peers regarding project status and issues and ensure project team goals are met
  • Oversees operational aspects of assigned clinical trial(s) and oversees clinical trial conduct including study start-up, enrollment, maintenance and close-out.
  • Prepares and/or contributes to development of study-related documents (e.g., Clinical protocols, Informed consent forms, Pharmacy Manual, Monitoring Plan, Case Report Form (CRFs), CRF Completion Guidelines and other relevant study plans, Clinical Study Report
  • Coordinates data review to support interim/final data analysis
  • Participates in study strategy development.
  • Maintains study timelines.
  • Contributes to development of study budget.
  • Contributes to development of RFPs and participate in selection of CROs/vendors.
  • Provide guidance and training to CROs, vendors such as IWRS, Central lab, eCOA, recruitment vendors, investigators and study coordinators on study requirements
  • Manages CRO interactions, including sponsor oversight of operational functional activities (e.g., study management, monitoring, site management).
  • Proactively identifies potential study issues/risks and recommends/implements solutions.
  • Organizes and manages internal team meetings, investigator meetings and other trial-specific meetings.
  • Participates in the recruiting and hiring process for CPA/CTMAs and supports their professional development
  • Coaches members of a work team and ensures adherence to established guidelines


Skills and Experience You Have:
  • Extensive clinical research knowledge and cross-functional understanding of clinical trial methodology
  • Extensive Study Start-up Experience
  • Global clinical trial experience
  • Prior involvement in Inflammation studies
  • Proficient in developing trial plans including site monitoring plans, risk mitigation strategies, site selection, and clinical supplies management
  • Highly developed leadership skills to successfully lead a clinical study team
  • Ability to deal with time demands, incomplete information or unexpected events
  • Must display strong analytical and problem solving skills
  • Attention to detail
  • Outstanding organizational skills with the ability to multi-task and prioritize
  • Excellent interpersonal, verbal and written communication skills are essential in this collaborative work environment
  • Comfortable in a fast-paced company environment and able to adjust workload based upon changing priorities


We are always excited to connect with great talent. This posting is intended for a [possible] upcoming opportunity rather than a live role. By expressing your interest, you'll be added to our talent pipeline and considered should this role become available.

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:

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.

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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.

About Syneos Health Careers

Syneos Health Careers

Joining Syneos Health presents an unparalleled opportunity to become part of a global team of professionals dedicated to biopharmaceutical solutions. At Syneos Health, job opportunities abound, offering a gateway to enhancing career paths in a company celebrated for its commitment to therapeutic and operational excellence.

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Syneos Health is at the forefront of healthcare innovation, collaborating on projects that integrate smart technology and human ingenuity to improve patient outcomes. This dynamic company is actively seeking professionals who are eager to drive progress in the biopharmaceutical field through diverse job opportunities ranging from scientific roles to operational positions.

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Syneos Health offers a variety of positions that cater to a range of skills and experiences, from entry-level to senior leadership roles. Employment at Syneos Health means contributing to a culture that values diversity and inclusion, ensuring every team member’s voice is heard and valued.

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