Clinical Research Coordinator Job in Fusion Technology Solutions

Key Responsibilities:

1. Trial Architecture:

> Contribute to the development of dynamic trial plans and protocols in tandem with the clinical operations team.

> Collaborate on the strategic selection and qualification of investigative sites.

2. Site Symphony:

> Conduct harmonious site initiation, monitoring, and close-out visits to ensure seamless protocol execution and pristine data collection.

> Cultivate collaborative relationships with investigative site teams, providing support and guidance.

3. Regulatory Mastery:

> Ensure meticulous adherence to regulatory standards, guidelines, and the principles of Good Clinical Practice (GCP).

> Spearhead the preparation and submission of regulatory documents to ethics committees and regulatory authorities.

4. Data Choreography:

> Direct the orchestration of data collection, ensuring the accuracy and completeness of clinical trial data.

> Collaborate with data management teams to resolve data discrepancies and maintain a symphony of data quality.

5. Risk Ballet:

> Proactively identify potential risks to trial success and choreograph mitigation strategies in collaboration with project teams.

6. Communication Sonata:

> Cultivate clear and resonant communication channels with internal and external stakeholders.

> Compose eloquent and timely study progress reports, fostering transparency and accountability.

Qualifications:

Bachelor\'s or advanced degree in a relevant field (Life Sciences, Nursing, etc.).

Demonstrated experience as a Clinical Research Associate, preferably in the pharmaceutical or biotechnology domain.

Profound knowledge of clinical trial processes, regulatory requirements, and GCP.

Exceptional interpersonal and communication finesse