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Role Overview:

  • Own the planning, execution, and oversight of clinical studies as clinical lead.
  • Serve as primary client contact and drive compliance with protocols and regulations.

Key Responsibilities:

  • Develop study documents, training materials, and recruitment/retention strategies.
  • Oversee site feasibility, start-up, monitoring, and eTMF implementation.
  • Collaborate with PM, CRAs, QA, and data management to ensure quality and timelines.

Qualifications:

  • Minimum 7 years of clinical research experience with strong monitoring background.
  • Bachelor's degree in science or health-related field; advanced degree preferred.
  • Professional working proficiency in English and experience with Microsoft Office.

Working Environment:

  • This is a remote role supporting Latin America with travel as needed.
  • The position offers significant growth into broader leadership and project management responsibilities.

Precision Medicine Group

Precision Medicine Group provides clinical development, regulatory, and commercial solutions for life sciences companies. It fosters a collaborative, high-integrity culture with opportunities for growth and leadership in a global remote environment.

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