Program Manager I – Biopharmaceutical

🔥 3 minutes ago

🧀 Wisconsin – Remote

🧀 Wisconsin – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

📋 Program 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

• Liaise with PPD operational departments, affiliates, and sponsors • Coordinate study setup, maintenance, and closure activities for identified protocols and study programs • Serve as local study coverage for global studies and point of contact for Clinical teams • Ensure timely completion of study activities and deliverables • Document communications and actions with sponsors or investigator sites • Manage existing Batch, Supply Only, and “In Conduct” studies • Develop new study setups in collaboration with the Tech Ops group • Provide backup coverage for centralized Project Management staff and Project Managers • Advise Project Managers on procedural and budgetary items, study modifications, and protocol amendments • Monitor monthly Budget-to-Burn reviews and contract modifications • Support initial study supply orders, supply templates, and shipment requests with Supply Chain Management • Monitor completion of shipment requests • Schedule internal and external meetings and teleconferences • Prepare and distribute agendas and meeting minutes • Monitor assignments and adjust priorities and work schedules to meet deadlines and deliver high-quality deliverables • Complete additional tasks supporting project, client, and departmental objectives

🎯 Requirements

• Bachelor's degree or equivalent and relevant formal academic / vocational qualification • Previous experience comparable to 0 to 2 years, or equivalent combination of education, training, and experience • Good organizational skills and ability to manage multiple assignments with changing priorities and challenging/conflicting deadlines • Effective project management and organizational skills • Good computer skills • General knowledge of clinical trial processes and programs • Strong attention to detail and problem-solving skills • Good written and verbal communication skills • Ability to effectively conduct oral presentations • Demonstrated experience identifying and resolving technical problems in a professional environment • Ability to maintain confidentiality with clinical teams • Ability to attain, maintain, and apply working knowledge of applicable procedural documents • Must be legally authorized to work in the United States without sponsorship • Must be able to pass a comprehensive background check, including drug screening • Ability to work in environments involving GMP safety standards, biological fluids, infectious organisms, hazardous materials, and required personal protective equipment • Ability to make occasional drives to site locations and occasional domestic travel

🏖️ Benefits

• Fully remote work arrangement • Standard Monday–Friday work schedule • Collaboration and development opportunities • Participation in a global team • Occasional domestic travel