Clinical Trial Manager - Remote

1w1 week ago

Labcorp

Carlsbad, US · Full-time · $140,000 – $175,000

About this role

Labcorp is a global leader in diagnostic testing and drug development solutions, helping healthcare providers, researchers, and patients make informed decisions that advance care. The Clinical Trial Manager plays a pivotal role, overseeing the successful planning, initiation, coordination, and execution of clinical trials. This contributes to groundbreaking advancements in laboratory diagnostics and patient care.

The Clinical Trial Manager ensures all team members verify that clinical trials adhere to stringent regulatory standards, Good Clinical Practice guidelines, and ethical norms. Responsibilities include protocol and database development, site identification, contracting and budget negotiation. They maintain data integrity within the study and from supporting labs providing assay results.

The role involves liaising with cross-functional teams, ensuring subject safety, and potentially overseeing trial sites at a monitoring level. The ideal candidate possesses scientific knowledge, meticulous attention to detail, and exceptional organizational and communication skills. They manage and lead a study team effectively.

Join Labcorp in the mission to improve health and improve lives through clinical research excellence. This US-based remote position offers opportunities to advance laboratory diagnostics and patient care initiatives. Contribute to studies that meet high standards of quality and compliance.

Requirements

Bachelor’s degree
3 or more years of experience in clinical research
3 or more years of experience with Microsoft Excel and Microsoft Word
3 or more years of experience in diagnostics
3 or more years of experience with device regulations for 510k and/or PMA submissions
3 or more years of experience with clinical protocol design
3 or more years of experience managing clinical study programs
3 or more years of experience with implementing clinical database management software

Responsibilities

Oversee the planning, initiation, coordination, and execution of clinical trials
Ensure adherence to regulatory standards, Good Clinical Practice guidelines, and ethical norms
Develop protocols and databases
Identify sites, negotiate contracts and budgets
Ensure data integrity within the study and from supporting labs
Liaise with cross-functional teams
Ensure subject safety
Oversee trial sites at a monitoring level