Study Manager - Cardiovascular

Syneos Health, Inc.; Morrisville (NC); On-site; USD 75,000 - 100,000; Full time

Benefits offered by this job

Medical, dental and vision coverage

Company match 401(k)

Flexible paid time off (PTO)

Job summary

Syneos Health, Inc. in Morrisville, NC is seeking a Project Manager to oversee interdisciplinary clinical research studies, ensuring compliance with regulatory standards. You will act as the primary liaison between the company and clients, managing timelines and budgets effectively.

The ideal candidate has a Bachelor's Degree in a relevant field and experience in clinical research organizations. Benefits include medical coverage, a company car or allowance, and flexible paid time off.

Qualifications

• Experience in a clinical research organization (CRO) and therapeutic area expertise preferred.
• Strong knowledge of Good Clinical Practice/ICH guidelines and applicable regulatory requirements.
• Willingness to travel as necessary (approximately 25%).

Responsibilities

• Manages the project as a project manager overseeing interdisciplinary clinical research studies.
• Acts as the primary liaison between the Company and the Customer.
• Leads project team to ensure quality, timelines, and budget management.

Skills

Organizational skills

Time management

Communication skills

Presentation skills

Interpersonal skills

Education

Bachelor's Degree in life sciences, Medicine, Pharmacy, or Nursing

Job description

Location: Morrisville, NC, United States

Job Overview

Syneos Health® is a fully integrated biopharmaceutical solutions organization accelerating customer success through clinical, medical affairs, and commercial insights.

Job Responsibilities

• Project Leadership and Delivery: Manages the project as a project manager overseeing interdisciplinary clinical research studies and ensures compliance with GCP, SOPs, and regulatory requirements.
• Acts as the primary liaison between the Company and the Customer to ensure timely study launch, conduct, and closeout according to the contractual agreement.
• Leads project team to ensure quality, timelines and budget management.
• Accountable for the financial performance of each project, coordinating activities and deliverables of all study conduct partners and proactively identifying and managing issues.
• Ensures studies are conducted in compliance with GCP, relevant SOPs and regulatory requirements.
• Responsible for quality and completeness of TMF for assigned projects.
• Maintains study information on various databases and systems.
• Manages study inspection readiness and oversees development and implementation of project plans.
• Plans, coordinates and presents at internal and external meetings; prepares project management reports for clients and management.
• Develops contingency planning and risk mitigation strategies to ensure successful delivery of study goals.
• Builds strong relationships with current clients to generate new and/or add-on business for the future.
• Participates in bid defense meetings as potential project manager.
• Might line‑manage other project management team members and clinical monitoring staff.

Qualifications

• Bachelor’s Degree (or equivalent) in life sciences, Medicine, Pharmacy, Nursing, or a comparable combination of education and experience.
• Experience in a clinical research organization (CRO) and therapeutic area expertise preferred.
• Strong knowledge of Good Clinical Practice/ICH guidelines and applicable regulatory requirements.
• Strong organizational and time‑management skills; able to work independently.
• Excellent communication, presentation, and interpersonal skills, written and spoken.
• Willingness to travel as necessary (approximately 25%).

Benefits

The benefits for this position may include a company car or car allowance, medical, dental and vision coverage, a company match 401(k), eligibility to participate in an Employee Stock Purchase Plan, eligibility to earn commissions/bonuses based on company and individual performance, and flexible paid time off (PTO) and sick time. Eligibility for paid sick time may vary depending on location in compliance with applicable regulations.

Salary

Salary range is based on company standards and may vary according to qualifications and experience.

EEO & Disability Statement

Any language contained herein is intended to fully comply with all obligations imposed by legislation in each country where the Company operates, including the EU Equality Directive. The Company is committed to compliance with the Americans with Disabilities Act and will provide reasonable accommodations as appropriate.