Early-Phase Clinical Scientist — Lead Trials

Parexel

Santa Fe (NM)

On-site

USD 120,000 - 160,000

Full time

48 hours ago
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Job summary

Parexel is seeking an Early Clinical Scientist to lead or support early phase clinical studies. The ECS will be accountable for clinical/scientific execution of the protocol and will coordinate with the Clinical Director and internal/external teams to ensure timely and compliant trial delivery.

The role requires experience in CRO management for Phase 1 trials, proficiency with CTMS/TCF systems, and strong scientific writing skills.

Qualifications

  • Experience in managing CROs from the Sponsor side for Phase 1 clinical trials.
  • Familiarity with early drug development processes.
  • Knowledge of GCP, ICH guidelines and regulatory requirements.

Responsibilities

  • Coordinate design, planning and execution of early phase clinical trials with Director and teams.
  • Oversee trials to ensure data validity and objective achievement.
  • Conduct on-site study monitoring, site training and supervision of complex endpoints.
  • Co-author clinical sections of protocols, investigator brochures and study reports.
  • Develop study operational documents (site monitoring plan, informed consent, etc.).
  • Review budgets and approve vendor invoices.

Skills

MS Office Suite
Team collaboration
English proficiency
Multitasking
Project management
Cross-functional collaboration
Scientific knowledge
Regulatory knowledge
Attention to detail

Education

Degree in Life Sciences
Bachelor’s degree and ≥7 years related* experience
Master’s degree and ≥5 years related* experience
PhD or doctorate degree and ≥1 year related experience

Job description

Parexel is seeking an Early Clinical Scientist to lead or support early phase clinical studies. The ECS will be accountable for clinical/scientific execution of the protocol and will coordinate with the Clinical Director and internal/external teams to ensure timely and compliant trial delivery.

The role requires experience in CRO management for Phase 1 trials, proficiency with CTMS/TCF systems, and strong scientific writing skills.

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