As a Project Manager II, you will be responsible for managing projects as a primary liaison between the company and the customer to ensure timely study launch, conduct, and closeout according to the customer's and company's contractual agreement.

Job Responsibilities

• Manage projects and ensure compliance with GCP, relevant SOP's, and regulatory requirements
• Act as a primary liaison between the company and the customer
• Lead project teams to ensure quality, timelines, and budget management
• Coordinate activities and deliverables of all study conduct partners
• Ensure studies are conducted in compliance with GCP, relevant SOP's, and regulatory requirements
• Develop contingency planning and risk mitigation strategies
• Develop strong relationships with current clients to generate new and/or add-on business
• Participate in bid defense meetings and line manage other project management team members and clinical monitoring staff

Qualifications

• Bachelor's degree 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
• Ability to manage time and work independently
• Direct therapeutic area expertise
• Excellent communication, presentation, and interpersonal skills
• Ability to travel approximately 25%

About Syneos Health

Syneos Health has 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.

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