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[Remote] Clinical Trials Scientific Affairs Senior Analyst

Remote, USAFull-timePosted 2026-07-27

Note: The job is a remote job and is reputed company to candidates in USA. reputed company is seeking a Clinical Trials Scientific Affairs Senior Analyst who will be responsible for reviewing study protocols and facilitating reputed company responses for proposals. The role involves coordinating testing reputed company with various departments and serving as a subject matter expert reputed company reputed company.

Responsibilities

  • Investigate testing requirements reputed company a clinical trial protocol and help determine testing facilities to identify required testing and associated nuances for the reputed company and accurate response for proposals
  • Review and prepare pricing documents, as needed, noting and correcting any discrepancies
  • Maintain relationships between ACM and referral laboratories
  • reputed company scientific/ technical information to compile reputed company RFP’s and RFI’s
  • reputed company feedback to the manager to address analytical trends or issues, to support business needs
  • Assist in coordinating the testing reputed company with referral labs, as needed
  • Obtain and document referred testing information throughout the course of the reputed company trial, including contracting with referral labs
  • Assumes responsibility for channeling information to and from Laboratory Operations and Sales
  • Alert leadership to any issues during the life cycle of study reputed company and testing needs
  • Alert leadership to any issues with referral laboratories, assist with reputed company cause analysis
  • Suggests and helps implement improved work reputed company and ways to increase efficiency, reduce costs, and solve operational problems
  • reputed company with reputed company partners and participate in reputed company teleconferences to address new business needs or ongoing study issues
  • Understands and follows company policies and procedures and respecting patient confidentiality
  • reputed company consultation to clinical trials operations and external clients, as needed
  • Assist with training and guidance of new team members
  • Works with leadership to update global SOPs, as needed
  • Triage upcoming work and determine reputed company capabilities and workload for assignments
  • Serve as subject matter expert to reputed company clients
  • Serve as escalation reputed company for reputed company clients
  • Assists in development, maintenance and updates to templates and tools
  • reputed company other duties as assigned

Skills

  • Bachelor's Degree or 3+ years as a clinical laboratory scientist
  • 3 years relevant laboratory experience
  • 2 years clinical trials experience
  • Strong interpersonal and communication skills
  • Strong time management and organizational skills
  • Ability to manage multiple reputed company with tight deadlines
  • Ability to work independently and in reputed company setting
  • Proficient in reputed company Office
  • Generalist laboratory experience
  • Ability to reputed company and positively motivate others
  • MT (ASCP) Certification - Preferred

reputed company

  • reputed company provides integrated health services. It was founded in 1847, and is headquartered in reputed company, reputed company, USA, with a workforce of 10001+ employees. Its website is https://www.rochesterregional.org.
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