Clinical Research Associate (CRA) - Pharmaceutical Trials

Placements24; Willows (CA); Remote; USD 85,000 - 120,000; Full time

Benefits offered by this job

Health benefits

Retirement plan

Bonuses

Professional development

Remote work

Job summary

Placements24 is seeking an experienced Clinical Research Associate (CRA) for a fully remote role. The CRA will monitor trial sites, ensure data integrity, and uphold patient safety and regulatory compliance from a home office.

The ideal candidate has a life sciences background, 3+ years of CRA experience, and strong skills in CTMS/EDC, with ability to travel occasionally for audits. Strong communication and organizational abilities are essential.

Qualifications

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or related field.
• Minimum of 3 years of CRA experience.
• Thorough understanding of clinical trial processes, GCP, and ICH guidelines.
• Experience monitoring multiple clinical trial sites.
• Ability to work independently in a remote setting.
• Proficiency with CTMS and EDC systems.
• Willingness to travel occasionally for site meetings or audits.
• Strong communication and organizational skills.

Responsibilities

• Conduct site visits (initiation, monitoring, close-out) according to protocol and SOPs.
• Assess protocol and CRF compliance by reviewing source documents.
• Ensure safety and rights of trial subjects and data integrity.
• Train and manage site staff, e.g., Study Coordinator.
• Build and maintain relationships with site staff and investigators.
• Manage study sites to ensure timely recruitment and data collection.
• Prepare monitoring visit reports and escalate site issues as needed.
• Ensure compliance with GCP, ICH, and local regulations.
• Oversee data quality and integrity from trial sites.

Skills

GCP knowledge

ICH guidelines

Site monitoring

Education

Bachelor's degree in Life Sciences

Tools

CTMS

EDC

Job description

About the Role

Our client, a global leader in pharmaceutical innovation, is seeking an experienced Clinical Research Associate (CRA) to join their expanding operations. This is a fully remote position, offering you the flexibility to contribute to critical clinical trials from the comfort of your home office. You will be responsible for monitoring clinical trial sites, ensuring data integrity, patient safety, and adherence to study protocols and regulatory requirements. This role is essential for the successful development of new life‑saving therapies. We are looking for a highly organized, detail‑oriented professional with a strong understanding of clinical trial processes and regulations. Your expertise will directly impact the advancement of novel pharmaceutical treatments. This position requires a commitment to ethical research practices and excellence in execution.

Key Responsibilities

• Conduct site visits (initiation, monitoring, and close‑out) according to protocol and company SOPs.
• Assess protocol and CRF (Case Report Form) compliance by reviewing source documents.
• Ensure the safety and rights of trial subjects are protected and that trial data are accurate, complete, and verifiable.
• Train and manage, through guidance, other appropriate individuals at the site, e.g., the Study Coordinator.
• Build and maintain a positive relationship with the site staff and investigators.
• Manage study sites, ensuring timely recruitment and data collection.
• Prepare monitoring visit reports and elevate site issues as necessary.
• Ensure compliance with Good Clinical Practice (GCP), ICH guidelines, and all applicable local regulations.
• Oversee the quality and integrity of data submitted from clinical trial sites.

Requirements

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
• Minimum of 3 years of experience as a Clinical Research Associate (CRA) or equivalent role.
• Thorough understanding of clinical trial processes, GCP, and ICH guidelines.
• Experience in monitoring multiple clinical trial sites.
• Excellent communication, interpersonal, and organizational skills.
• Ability to work independently and manage time effectively in a remote setting.
• Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Willingness to travel occasionally if required for specific site meetings or audits (though primarily remote).
• Strong problem‑solving skills and attention to detail.

Benefits

• This remote role offers a competitive salary, comprehensive health and wellness benefits, a retirement savings plan, and ample opportunities for professional development and career advancement within a leading pharmaceutical company.
• Enjoy the flexibility and work‑life balance that comes with a remote position.
• Our client invests in continuous training and provides access to industry‑leading technology and resources.
• Performance‑based bonuses are also a part of the compensation package.