Project Manager - Future Roles (UK)

Project Manager - Future Roles (UK)

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.

Every day we perform better because of how we work together, as one team, each the best at what we do. We bring a wide range of talented experts together across a wide range of business critical services that support our business. Every role within Corporate is vital to furthering our vision of Shortening the Distance from Lab to Life .

WORK HERE MATTERS EVERYWHERE

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 our Total Self culture - where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
• We are continuously building the company we all want to work for and our customers want to work with. When we bring together diversity of thoughts, backgrounds, cultures, and perspectives, we create a place where everyone feels like they belong.

Job Responsibilities

• Project Leadership and Delivery. Manage a project as a project manager overseeing interdisciplinary clinical research studies and ensuring compliance with GCP, relevant SOP's, and regulatory requirements.
• Act as the primary liaison between the Company and the Customer to ensure timely study launch, conduct, and closeout according to contractual agreements.
• Lead the project team to ensure quality, timelines, and budget management.
• Accountable for the financial performance of each project. Coordinate activities and deliverables of all study conduct partners and proactively identify and manage issues.
• Maintain the quality and completeness of TMF for assigned projects.
• Maintain study information in a variety of databases and systems.
• Manage study management components of inspection readiness for all aspects of the study conduct. Oversee development and implementation of project plans.
• Plan, coordinate and present at internal and external meetings. Prepare project management reports for clients and management.
• Develop contingency planning and risk mitigation strategies to ensure successful delivery of study goals.
• Build strong relationships with current clients to generate new and/or add on business for the future.
• Participate in bid defense meetings where presented as a potential project manager.
• Line manage other project management team members and clinical monitoring staff, when required.

Qualifications

• Bachelor's Degree (or equivalent) in life sciences, Medicine, Pharmacy, Nursing or equivalent combination of education and experience.
• Clinical research organization (CRO) and relevant therapeutic experience preferred. Strong knowledge of Good Clinical Practice/ICH guidelines and other applicable regulatory requirements.
• Strong organizational skills and ability to manage time and work independently.
• Direct therapeutic area expertise.
• Ability to embrace new technologies.
• Excellent communication, presentation, interpersonal skills, both written and spoken.
• Ability to travel as necessary (approximately 25%).

About Us

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.

Equal Opportunity Statement

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.

All employment decisions are made without regard to race, color, religion, sex, national origin, ancestry, genetics, age, disability, or veteran status in accordance with applicable state, federal, and local laws.