Clinical Trials Coordinator

2 weeks ago


San Mateo, California, United States ACL Digital Full time

Position: Clinical Trial Associate

Location: Remote

Role Overview:

The Clinical Trial Associate is a vital member of the Clinical Operations team, focusing on the execution of clinical trials across various therapeutic areas. This role is essential in ensuring that all clinical studies are conducted in compliance with established protocols, company policies, and regulatory standards.

Key Responsibilities:

  • Act as the primary contact for operational aspects of clinical trials, collaborating with internal teams and external partners.
  • Participate in the planning and coordination of all activities related to the collection and analysis of biological samples.
  • Provide expertise in sample management to ensure high-quality biological samples are collected ethically and in accordance with regulatory requirements.
  • Oversee day-to-day interactions with laboratory vendors to ensure timely and accurate data delivery.
  • Evaluate scientific proposals and protocols to assess feasibility for clinical operations.
  • Foster strong relationships with cross-functional teams to facilitate the efficient execution of clinical study strategies.
  • Identify potential operational challenges and develop resolution plans in collaboration with senior team members.
  • Organize and lead operational meetings with study teams and vendors.
  • Maintain accurate databases and documentation related to clinical operations.
  • Review and interpret study documents, ensuring compliance with protocol requirements.
  • Contribute to the development of study plans, informed consents, and other essential documentation.
  • Assist in the preparation of study reports and presentations, ensuring clarity and accuracy of information.

Qualifications:

We seek candidates with diverse backgrounds who can contribute uniquely to our mission. The following qualifications are essential:

  • Advanced degree in life sciences or a related field with relevant clinical experience.
  • Demonstrated ability to adapt to changing environments and manage multiple projects effectively.
  • Strong understanding of clinical study management best practices and regulatory guidelines.
  • Familiarity with medical and scientific terminology.

This role requires a proactive approach and the ability to work collaboratively within a dynamic team environment.



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