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Full-time

Clinical Research Associate - 174832 - 175212 - 175800

$110K/yr – $125K/yr

Conduct site qualification, initiation, routine monitoring, and closeout visitsScience & PharmaceuticalPosted 22d ago

You'll complete your application on the employer's website.

Job description

Piper Companies is recruiting a Clinical Research Associate for an unnamed leading organization in the pharmaceutical/biotechnology industry. The role supports clinical study execution through site monitoring, compliance review, issue resolution, and relationship-building with investigative sites.

Tags

Government

Information Technology

Software

Information Services

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Responsibilities

Conduct site qualification, initiation, routine monitoring, and closeout visits

Ensure studies are conducted in compliance with ICH-GCP guidelines, protocols, and regulatory requirements

Review source documentation, site records, and data for accuracy and compliance

Build and maintain strong relationships with investigators and site staff

Identify, document, and resolve site issues while supporting overall study execution

Complete monitoring reports and follow-up documentation within required timelines

Travel extensively to clinical research sites as required

Preferred

Bachelor's degree in a scientific, healthcare, or related field preferred

Experience within pharmaceutical, biotechnology, or medical device studies preferred

Benefits

Comprehensive benefits package including medical, dental, vision, 401(k), and PTO

Direct-hire opportunity with long-term career growth

Remote workplace

Technical and professional services for U.S. government.

Mclean, Virginia, USA

http://zacharypiper.com/

Distribution of Different Job Fields Receiving Sponsorship

Represents job field similar to this job

Engineering and Development

Trends of Total Sponsorships

*2022

(1)

2021

Growth Stage

Total Funding

$3M

2018-02-22

Series Unknown· $1.3M

2014-04-10

Series Unknown· $1.7M

Leadership Team

Justin Jordan

Founder and Chairman

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Qualifications

2+ years of independent monitoring experience as a Clinical Research Associate

Strong knowledge of ICH-GCP guidelines and clinical trial regulations

Excellent communication, organization, and problem-solving skills

Bachelor's degree in a scientific, healthcare, or related field preferred

Experience within pharmaceutical, biotechnology, or medical device studies preferred

2+ years of independent monitoring experience as a Clinical Research Associate.

Required skills

Clinical Trial Monitoring, ICH-GCP, Clinical Trial Regulations, Pharmaceutical, Biotechnology, and Medical Device Studies

Experience

2+ years

Interested in this role?

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