Single Sponsor Associate Clinical Project Director (Program Manager) – 3 days in the Dublin office

About the Opportunity

Single Sponsor Associate Clinical Project Director (Program Manager) - 3 days in the Dublin office

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.

Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.

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 accelerate the delivery of therapies, because we are passionate to change lives.

Discover what our 29,000 employees, across 110 countries already know:

WORK HERE MATTERS EVERYWHERE

Responsibilities

• Manages a project as a Project Manager overseeing interdisciplinary clinical research studies and/or programs
• Ensures compliance with GCP, relevant SOP’s and regulatory requirements
• Acts as primary liaison and/or facilitator between the Company and the Customer
• Leads project team to ensure quality, timelines and budget management
• Develops contingency planning and risk mitigation strategies
• Maintains and evaluates project progress
• Develops strong relationships with current and prospective clients
• Responsible for quality and completeness of TMF for assigned projects
• Demonstrates mastery of current business unit therapeutic environment and drug development trends
• Serves as team leader and line manages and mentors other project management and clinical monitoring staff

About You

Bachelor’s Degree (or equivalent) level of qualification in life sciences, Medicine, Pharmacy, Nursing or equivalent combination of education and experience. Ideally Project Management qualified i.e. Prince II or PMP / equivalent.

Strong knowledge of Good Clinical Practice/ICH guidelines, regulatory requirements, drug development process and clinical monitoring procedures.

Ability to embrace new technologies. Excellent communication, presentation, and interpersonal skills, both written and spoken, with an ability to inform, influence, convince, and persuade. Ability to travel as necessary (approximately 60%).

Eligibility

Clinical research organization (CRO) and relevant therapeutic experience preferred

Benefits

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.

About Company

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