Senior Bioanalytical Study Manager

🔥 1 hour ago

🌲 North Carolina – Remote

🌲 North Carolina – Remote

⏰ Full Time

🟠 Senior

👔 Manager

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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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

• Lead and maintain direct oversight of a portfolio of client projects • Manage overall project and portfolio performance, including resources, budgets, and prioritization • Serve as the primary operational interface and chief liaison between PPD and the client • Negotiate and make real-time decisions with clients • Provide oversight and coordination to internal departments and external clients • Facilitate technical and clinical laboratory information flow among stakeholders • Prepare and maintain project specifications, budgets, contracts, and version-controlled master files • Ensure sponsor authorization and compliance before services are delivered • Ensure compliance with FDA, Good Clinical Practice, PPD SOPs, personnel policies, exposure control plans, and biological specimen transport regulations • Coordinate internal groups and support staff to resolve procedural, budgetary, and documentation issues • Manage day-to-day project activities, resolve issues, and answer queries • Consult with IT and data management groups on software and functionality for project management • Support RFP feasibility assessments and draft proposal responses with BD and finance teams • Take responsibility for accurate invoicing and coordinate billing for the client's portfolio

🎯 Requirements

• Bachelor's degree or equivalent and relevant formal academic / vocational qualification • 5+ years of previous relevant experience, or equivalent combination of education, training, and experience • Strong science and/or business acumen • Strong verbal, written, and presentation skills • Superior time management, planning, and organizational skills • Proven analytical skills • Demonstrated compliance with procedures and policies • Ability to perform multiple tasks effectively in a stressful environment • Extensive knowledge and experience in Project Management • Strong client relationship management skills • Ability to work effectively with multi-level teams • Ability to work in a fast-paced undefined environment • Strong negotiation skills • Ability to work in a laboratory and/or clinical environment • Ability to undertake occasional drives to site locations and occasional domestic travel • Ability to work with potential exposure to biological fluids and infectious organisms • Ability to use required personal protective equipment such as protective eyewear, garments, and gloves

🏖️ Benefits

• Healthy and balanced work environment • Collaboration and development opportunities • Personal protective equipment provided/required for the role