Associate Country Project Manager

🔥 0 minutes ago

🌲 North Carolina – Remote

🌲 North Carolina – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

👷‍♀️ Project Manager

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 10%

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Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1956

🏥 Healthcare

📦 Logistics

🏭 Manufacturing

Healthcare • Logistics • Manufacturing

Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.

📋 Description

• Manage assigned studies to deliver within agreed schedules and quality requirements • Execute the prime contract locally by implementing global study strategy and proactively managing risks • Represent the company to external stakeholders and provide excellent customer service • Lead assigned low- to moderate-complexity projects with global, territorial, and site-level oversight • Support senior CPMs on more complex studies • Coordinate or collaborate on study start-up activities, site qualification and initiation visits, and ethics committee and regulatory submissions • Identify and manage rate-limiting factors such as drug supply and vendors to support recruitment • Collect and analyze study metrics, review project tracking tools, provide status updates, identify risks, and implement recovery actions • Monitor recruitment methods, patient pre-identification, processing, and retention against targets • Set up, organize, maintain, and archive relevant local Trial Master File sections and study logs • Collaborate with clinical and other departments to meet project deliverables • Communicate with study sites regarding protocol, patient participation, case report forms, and other study matters • Lead team meetings and maintain timelines, resources, interactions, and quality • Escalate budget needs to management and finance and support invoicing and query resolution • Act as overall study lead for local studies from award through close-out, including budget, contracts, and client discussions about patient allocation

🎯 Requirements

• Bachelor's degree or equivalent and relevant formal academic / vocational qualification • 2+ years of previous experience providing the knowledge, skills, and abilities to perform the job • Equivalent combinations of appropriate education, training and/or directly related experience may be considered sufficient • Good planning and organizational skills • Solid interpersonal and problem solving skills for working in a multicultural matrix organization • Ability to work effectively in changing environments with complex/ambiguous situations • Familiarity with clinical research practices, processes, and requirements • Good judgment and decision-making skills • Effective oral and written communication skills, including English language proficiency • Ability to evaluate workload against project budget and adjust resources accordingly • Financial acumen and knowledge of budgeting, forecasting and fiscal management • Strong attention to detail • Understanding of relevant regulations, including ICH/GCP and FDA guidelines • Good computer skills using Outlook, Excel, Word, and similar applications • Ability to perform required physical activities, including frequent stationary work, mobility, occasional lifting of 15–20 lbs, and regular attendance • Occasional domestic and international travel and drives to site locations