Clinical Project Manager Job at Somewhere, Latin America

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  • Somewhere
  • Latin America

Job Description

POSITION OPEN ONLY FOR LATAM REGION AND THE PHILIPPINES 
100% REMOTE POSITION

Position : Clinical Project Manager

Working Hours: Â US Working hours - EST

Salary Range:Â $3,000 - $4,500 Usd Based on experience
Type of Contract : Independent Contractor Agreement

 

The Clinical Project Manager (CPM) is responsible for the overall coordination, implementation, execution, and delivery of clinical trials within timelines, budget, and scope. Working within a Contract Research Organization (CRO) environment, the CPM ensures that all clinical project activities are conducted in accordance with applicable regulatory guidelines, client expectations, and standard operating procedures (SOPs).

Key Responsibilities:

  • Lead and manage the planning and execution of clinical trials from initiation through close-out.

  • Serve as the primary point of contact for clients and internal teams, ensuring alignment and communication throughout the project lifecycle.

  • Develop project plans, timelines, and budgets; track progress and report status to stakeholders.

  • Coordinate and oversee cross-functional project teams, including clinical monitors, data management, biostatistics, regulatory affairs, and medical writing.

  • Identify potential project risks and develop mitigation strategies.

  • Ensure compliance with ICH-GCP, regulatory requirements, SOPs, and client specifications.

  • Oversee site selection, initiation, monitoring, and closeout activities in collaboration with clinical operations staff.

  • Maintain and manage trial master files and ensure proper documentation.

  • Provide leadership, mentoring, and training to project team members as needed.

  • Participate in proposal development and bid defense meetings when required.

Qualifications:

  • Minimum of 4–6 years of experience in clinical research, with at least 2 years in a project management role within a CRO or pharmaceutical company.

  • Strong knowledge of ICH-GCP and global regulatory requirements.

  • Demonstrated ability to manage multiple projects simultaneously.

  • Excellent organizational, leadership, and communication skills.

  • Proficiency in project management tools and MS Office Suite.

  • Ability to travel as needed (domestic and international).

Preferred Attributes:

  • PMP certification or equivalent is a plus.

  • Experience in specific therapeutic areas (e.g., oncology, CNS, cardiology) is an advantage.

  • Familiarity with electronic data capture (EDC) systems and clinical trial management systems (CTMS).

Job Tags

Contract work, For contractors,

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