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.
Analytical Instruments • Laboratory Supply Chain Programs and eCommerce • Laboratory Equipment • Lab Services • Specialty Diagnostics
March 4
🏄 California – Remote
🌽 Illinois – Remote
💵 $82.8k - $140k / year
⏰ Full Time
🟠 Senior
😶🌫️ Therapist
🦅 H1B Visa Sponsor
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.
Analytical Instruments • Laboratory Supply Chain Programs and eCommerce • Laboratory Equipment • Lab Services • Specialty Diagnostics
• Perform and coordinate all aspects of the clinical monitoring and site management process • Conduct remote and on-site visits to assess protocol and regulatory compliance • Ensure data accuracy through SDR, SDV and CRF review as applicable • Document observations in reports and letters in a timely manner • Escalate observed deficiencies and issues to clinical management • Maintain regular contact with investigative sites • Conducts monitoring tasks according to approved monitoring plans • Participate in investigator payment process • Identify potential investigators in collaboration with the client company • Initiate clinical trial sites according to relevant procedures • Ensure required essential documents are complete and in place • Provide trial status tracking and progress update reports • Facilitate effective communication through written, oral, and/or electronic contacts
• Bachelor’s degree in a life science related field or Registered Nursing certification or equivalent • Previous experience comparable to 1+ years as a clinical research monitor for CRA (Level II) • Previous experience comparable to 2+ years for Sr CRA (Level I) • Previous experience comparable to 3+ years for Sr CRA (Level II) • Considerable clinical research monitoring experience comparable to 5+ years for Principal CRA • Valid driver’s license where applicable • Ability to provide reasonable accommodation during the job application process as necessary
• Competitive remuneration • Annual incentive plan bonus • Healthcare and a range of employee benefits • 120 hours paid time off (PTO) • 10 paid holidays annually • Paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave) • Accident and life insurance • Short- and long-term disability in accordance with company policy • Retirement and savings programs, such as competitive 401(k) • Employees’ Stock Purchase Plan (ESPP) offers the opportunity to purchase company stock at a discount
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