01Requirements
Bachelor Degree in Life Science is Preferred12+ year of Experience in Clinical Monitoring, Trial Management, eTMF management, Onsite Monitoring related activitiesShould have experience in Managing CRAs, CTCs, Project Support Coordinators for More than 4+ YearsShould have experience in managing one or multiple FSP Clients as Single Point of ContactShould have experience in Workflow Allocation, Performance Management, Quality/CAPA, Reporting related activitiesShould be willing to Travel to Clinical Trial Sites across India (up to 25% Travel)
Knowledge, Skills and Abilities:
Advanced mentoring/leadership/supervisory skills
Excellent clinical trials monitoring skills; Remote and on-site
Demonstrated understanding of or ability to learn the companys SOPs, WPDs, and relevant regulations (e.g. ICH/GCP, FDA guidelines)
Demonstrated ability to evaluate medical research data
Strong organizational and negotiation skills
Strong attention to detail
Advanced written and oral communication skills
Good knowledge of English language and grammar
Demonstrated use of computer to include data entry, archival and retrieval
Ability to travel as needed
Excellent teammate with team building skills
Excellent interpersonal and conflict resolution skills
Advanced ability to utilize problem-solving techniques applicable to constantly changing environment
Solid knowledge of medical/therapeutic areas and medical terminology
Why Join Us
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. Youll work in an environment where collaboration and development are part of the everyday experienceand where your contributions truly make a difference.
Apply today to help us deliver tomorrows .
