Clinical trials associate vs senior program coordinator

Differences between clinical trials associate and senior program coordinator duties and responsibilities

Clinical trials associate example responsibilities.

• Manage trial master files and study document to meet GCP/ICH and internal guidelines for records retention.
• Audit TMF to ensure all require regulatory documentation are collected and lead.
• Work closely with investigators to recruit eligible patients to clinical protocols, manage data collection and preparation.
• Preform ICF customization in accordance with ICH guidelines, GCP s and local regulatory requirements.
• Support the setup, data entry and QC of the system to ensure accuracy and quality of data.
• Monitor clinical data and resolve inconsistencies according to FDA regulations and ICF guidelines.
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Senior program coordinator example responsibilities.

• Manage co-op vendor and provide overall program direction for Toyota dealers and regional offices nationwide.
• Report metrics associate with assign compounds to QA management, clinical development clinical development staff, and contract research organization staff.
• Participate at PPT's and participate in the development of IEP's and strategies to meet IEP objectives.
• Coordinate RFP policies and processes for all grant programs to ensure consistency.
• Collaborate with home inspector to create scope of work, prepare RFP s to secure construction bid quotes from rehabilitation contractors.
• Schedule and facilitate all IEP meetings, gathering information, inviting participants and encouraging parent participation.
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