Senior Clinical Research Associate (Remote/Travel-Ready)

Parexel; Concord (NH); On-site; USD 70,000 - 100,000; Full time

Job summary

Parexel FSP is seeking a CRA/Sr CRA in the United States to oversee clinical trial activities at assigned sites, ensuring adherence to study plans and local regulatory requirements.

The CRA will monitor, initiate, and close sites, manage regulatory documents, and coordinate with the Local Study Team to achieve study commitments. Strong English communication, attention to detail, and the ability to travel are essential.

Qualifications

• Excellent knowledge of ICH-GCP and GMP/GDP basics.
• Bachelor’s degree in life sciences or equivalent.
• Ability to travel nationally/internationally.

Responsibilities

• Monitor sites per Monitoring Plan and SDR/SDV as required.
• Coordinate with LSAD/LST to ensure timely site initiation, activation and closure.
• Maintain site regulatory documentation (ISF, essential documents) and CTMS/eTMF updates.
• Ensure data quality and timely reporting of SAEs and site performance.
• Escalate quality issues per Parexel procedures and client SOPs.

Skills

Attention to detail

Written communication

Interpersonal skills

English proficiency

Education

Bachelor's degree in Life Sciences

Tools

CTMS

eTMF

Job description

Parexel FSP is seeking a CRA/Sr CRA in the United States to oversee clinical trial activities at assigned sites, ensuring adherence to study plans and local regulatory requirements.

The CRA will monitor, initiate, and close sites, manage regulatory documents, and coordinate with the Local Study Team to achieve study commitments. Strong English communication, attention to detail, and the ability to travel are essential.