Remote Senior Clinical Research Associate – Oncology

Parexel

Santa Fe (NM)

Remote

USD 90,000 - 130,000

Full time

2 days ago
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Job summary

Parexel is seeking a Clinical Site Monitoring professional to oversee trial conduct and site performance across Oncology and non-Oncology programs. The role emphasizes partnerships with SCP, site personnel coaching, and ensuring compliance with SMP, SOPs and regulatory requirements.

The ideal candidate has extensive monitor experience, strong English and local language skills, and willingness to travel 60-80% within the region, with some international travel and weekends as needed.

Qualifications

  • Extensive knowledge of clinical trial methodologies, ICH/GCP, FDA and local country regulations.
  • Ability to work in a matrix team environment and influence delivery.

Responsibilities

  • Ensure proper conduct of clinical trials in accordance with SMP and applicable laws to achieve project goals.
  • Manage assigned operational aspects for implementation of clinical trial activities at investigator sites from activation to database lock.
  • Serve as primary point of contact for assigned investigator sites and coordinate with SCP for site delivery quality.
  • Monitor safety events and ensure timely reporting and resolution with Drug Safety Unit.
  • Submit required reports and maintain TMF documentation within deadlines.
  • Provide enrollment support and assist with recruitment initiatives at site level.

Skills

Clinical trial methodologies
ICH/GCP compliance
Regulatory knowledge
English fluency
Travel readiness
Communication skills
Site monitoring experience

Education

Bachelor’s degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical background or equivalent

Job description

Parexel is seeking a Clinical Site Monitoring professional to oversee trial conduct and site performance across Oncology and non-Oncology programs. The role emphasizes partnerships with SCP, site personnel coaching, and ensuring compliance with SMP, SOPs and regulatory requirements.

The ideal candidate has extensive monitor experience, strong English and local language skills, and willingness to travel 60-80% within the region, with some international travel and weekends as needed.

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