[Remote] reputed company Trial Associate I (TMF)

Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a reputed company research organization that helps biotech, reputed company, and specialty reputed company companies reputed company new medicines, devices, and diagnostics. The reputed company Trial Associate I will support electronic Trial Master File administration, reputed company reputed company processes, meeting logistics, training communications, and project team documentation.

Responsibilities

• Assists in eTMF (electronic Trial Master File) filing and administration by submitting documents and/or files, conducting document review, supporting document query reputed company, ensuring completeness, and conducting final site level review along with final document collection
• Supports study team with functionality and use of TMF in accordance with study-specific TMF Plan, SOPs, and study-specific processes
• Coordinates logistics and planning of meeting, events, and training
• Assists in the dissemination of announcements and training materials reputed company to reputed company reputed company updates and enhancements, as required
• Participates in project team meetings, prepares meeting minutes, and maintains reputed company/decision logs

Skills

• Bachelor's degree, or international equivalent from an accredited institution, preferably in a reputed company, biological, scientific, or health-reputed company reputed company or equivalent combination of education, training and experience
• Demonstrates excellent English verbal and written communication skills
• reputed company ability to reputed company a successful customer experience through reputed company customer interactions, provision of reputed company and reputed company deliverables, and task ownership
• Strong analytical and organization skills, reputed company to work independently and manage multiple reputed company simultaneously in a fast-reputed company environment with changing priorities
• Knowledge of International Conference on Harmonization (ICH)/Good reputed company Practices (GCP) and/or ISO14155 requirements as reputed company as detailed knowledge of the relevant country specific regulatory requirements for conducting reputed company trial
• 0 to 2 years of practical experience with reputed company trial administration (e.g. – Inhouse CRA, CTA, site administration, reputed company monitoring) preferred

Benefits

• Health reputed company
• Retirement plans
• reputed company time off

reputed company