Senior Clinical Project Manager, Associate Director – Global Role, Multisponsor

🕒 4 days ago

🌵 Arizona, Maine, +3 more states – Remote

🌵 Arizona – Remote 🦞 Maine – Remote 🌲 North Carolina – Remote 🏈 Ohio – Remote ⚓ Rhode Island – Remote

💵 $114k - $210.9k / year

⏰ Full Time

🟠 Senior

👷‍♀️ Project Manager

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Syneos Health

WebsiteLinkedInAll Job Openings

10,000+ employees

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

Biotechnology • Pharmaceuticals • Healthcare Insurance

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.

📋 Description

• Manages a project as Project Manager overseeing interdisciplinary clinical research programs ensuring compliance with Good Clinical Practices (GCPs), relevant Standard Operating Procedures (SOPs) and regulatory requirements • Acts as primary liaison between the Company and the Customer to ensure project launch, conduct, and closeout according to the Customer’s and the Company's contractual agreement • Leads clinical team to ensure quality, timelines and budget management • Accountable for the financial performance of assigned projects • Accountable for all project deliverables for assigned projects and/or project regions • Coordinates activities and deliverables of all project conduct partners and proactively identifies and manages issues • Maintains and evaluates project progress by maintaining timelines and other tracking/analysis tools • Responsible for project management components of inspection readiness for all aspects of the project conduct, including Trial Master Files • Prepares project management reports for clients and management

🎯 Requirements

• Bachelor’s Degree (or equivalent) level of qualification in life sciences, Medicine, Pharmacy, Nursing or related field or equivalent combination of education and experience • Strong knowledge of Good Clinical Practice/ICH guidelines, regulatory requirements, drug development process and clinical monitoring procedures • Clinical research organization (CRO) and relevant therapeutic experience preferred • Strong ability to manage time and work independently • Ability to embrace new technologies • Excellent communication, presentation, interpersonal skills, both written and spoken • Flexibility and the ability to mentor and manage new staff and to handle multiple tasks to meet deadlines delivering high quality work in a dynamic environment • Ability to travel as necessary (approximately 25%)

🏖️ Benefits

• 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 • Flexible paid time off (PTO) and sick time