Remote Senior Clinical Research Associate (Oncology)

Parexel

Frankfort (KY)

Remote

USD 90,000 - 120,000

Full time

7 days ago
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Job summary

Parexel is seeking an experienced clinical monitoring professional to oversee monitoring responsibilities across oncology and non-oncology studies in the United States, with substantial travel. You will ensure compliant conduct of trials, manage site relationships, and support recruitment and site activation efforts.

The role requires at least 3 years of monitoring experience, strong knowledge of GCP/ICH, and flexibility for 60–80% travel, including potential international assignments.

Qualifications

  • Extensive knowledge of clinical trial methodologies, ICH/GCP, FDA regulations and local country rules.
  • Monitoring experience of at least 3 years in clinical research site monitoring, oncology preferred.
  • Fluent in English and local language(s) of the country of work.

Responsibilities

  • Oversee monitoring responsibilities and study conduct to ensure quality, timelines and compliant execution according to SMP and SOPs.
  • Manage operational aspects from site activation through database lock with timely and quality deliverables.
  • Act as primary contact for investigator sites and collaborate with SCP to ensure site delivery quality.
  • Coordinate with the study team, vendors, and sites to facilitate information flow and issue resolution.
  • Provide site staff training to ensure protocol adherence and patient safety.

Skills

Clinical trial methodologies
Monitoring experience
English fluency
60-80% travel
Driver’s license & passport
Global clinical trial experience

Education

Bachelor’s degree in life sciences

Job description

Parexel is seeking an experienced clinical monitoring professional to oversee monitoring responsibilities across oncology and non-oncology studies in the United States, with substantial travel. You will ensure compliant conduct of trials, manage site relationships, and support recruitment and site activation efforts.

The role requires at least 3 years of monitoring experience, strong knowledge of GCP/ICH, and flexibility for 60–80% travel, including potential international assignments.

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