Start-up Manager, FSP

🕒 October 23

🌲 North Carolina – Remote

🌲 North Carolina – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

👔 Manager

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 10%

What it means: the chance that no one is really hiring for this job.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

• Collaborate with matrixed team members to deliver site activation for assigned projects • Oversee site activation according to timelines and quality standards • Coordinate information flow between PPD teams, clients, and functional departments • Develop project implementation plans and guidelines using PPD tools • Monitor and analyze project status, completion, and metrics for upper management • Identify risks and develop contingency plans • Manage financial and contractual aspects related to site activation • Establish controls to align project resources and expenses with budgets • Administer technical and operational site activation activities, including feasibility, site contracts, and country-team coordination • Manage assigned scope against timelines, costs, and quality • Identify and evaluate issues affecting successful site activation and implement solutions • Develop customer relationships aligned with assigned projects • Work in office, laboratory, and/or clinical environments • Handle potential exposure to biological fluids, infectious organisms, and electrical office equipment • Use required personal protective equipment • Travel up to 20% to domestic and international site locations • Work upright and/or stationary for 6–8 hours daily, with frequent mobility and occasional lifting up to 15–20 lbs

🎯 Requirements

• Bachelor's degree or equivalent and relevant formal academic / vocational qualification • 5+ years of comparable experience • Equivalency through a combination of appropriate education, training and/or directly related experience may be considered • Ability to work efficiently with cross-functional teams • Knowledge of cross-functional project management principles • Organizational, multitasking, and attention-to-detail skills • Ability to identify and remedy risks related to contractual deliverables • Cross-cultural awareness and adaptability • Comprehensive understanding of clinical research/development, medical and therapeutic areas, study phases, and medical terminology • Ability to lead, liaise, and coordinate cross-functional project teams • Comprehensive knowledge of clinical development guidelines and Directives • Ability to use in-house and off-the-shelf computer software • Ability to communicate and understand information effectively • Ability to work under stress and multitask • Regular and consistent attendance

🏖️ Benefits

• Global team environment • Collaboration and development opportunities • Occasional travel to site locations, including domestic and international travel

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