Clinical Trial Coordinator

Work Schedule

Environmental Conditions

Job Description

Join our team as a Clinical Trial Coordinator!

As a Clinical Trial Coordinator at Thermo Fisher Scientific Inc. you will be part of an outstanding team committed to making a tangible impact on global health. This is an outstanding chance to contribute to groundbreaking scientific research and be at the forefront of innovation.

Key Responsibilities

• Coordinate and maintain clinical trial protocols and documentation.
• Ensure flawless execution of trial logistics and timelines.
• Assist in the preparation of regulatory submissions and compliance documentation.
• Evaluate trial progress and report findings to senior management.
• Collaborate with cross-functional teams to determine and implement trial strategies.

Required Qualifications

• Proven experience in clinical trial administration or a related field.
• Strong organizational skills and attention to detail.
• Ability to strictly adhere to regulatory standards and company protocols.
• Excellent communication and collaboration abilities.
• Ambitious approach with the drive to successfully implement trial initiatives.

Role Description

• Provides administrative and technical support to the Project Team. Supports audit readiness by ensuring files are reviewed according to the schedule detailed in the organizations SOP and department guidance document. Provides administrative support for site activation activities. Aids the development of the critical path for site activation within assigned projects in support of rapid site activations. Represents the organization in the global medical research community. May develop collaborative relationships with investigators and site personnel to conduct feasibility assessments in accordance with feasibility processes and within expected timelines. May develop a local knowledge base of sites in the respective market through collaboratively working with local company personnel. May apply local knowledge organization systems external site lists and sponsor directives to develop and review site lists that are suitable for the strategic needs of feasibility activities and to provide local input into the site tiering process. May act as a buddy during onboarding phase. Supports training of new staff and participates in departmental initiatives to aid in process improvements/enhancements.

Why Thermo Fisher Scientific

At Thermo Fisher Scientific Inc. we cultivate an inclusive and cooperative atmosphere where diverse viewpoints are appreciated. You will have the opportunity to excel at the highest level while contributing significantly to patient outcomes. Our dedication to your professional development and our common goal makes this role extraordinarily fulfilling.

Be a part of our dedicated team that is passionate about ingenuity and high standards. Your involvement will be vital in our quest to empower our clients to foster a healthier cleaner and safer world!