CRF Specialist, Early Phase Clinical Research- Dallas, TX

About the role

As one of the largest Clinical Research Organizations in the world, we are seeking a CRF Specialist to manage study data, collaborate with various stakeholders, and contribute to the safety and efficacy of new drugs.

Responsibilities

• Transcribe and enter study data into case report forms using Metadata.
• Collaborate with quality control and project management teams to ensure timely completion.
• Address data questions and classifications during sponsor monitoring visits.
• Resolve sponsor-generated data queries promptly.
• Communicate effectively with data managers and CRAs, adhering to study protocols and SOPs.
• Perform other duties as needed or assigned.

Requirements

• High school diploma or equivalent.
• One to two years’ experience in a research environment or related experience.
• Strong attention to detail and accuracy.
• Excellent communication and organizational skills.
• Ability to work collaboratively with a team.

Qualifications

• Fortrea may consider relevant and equivalent experience in lieu of educational requirements.

Skills

• Experience in clinical research or related field is a plus.

Benefits

Regular, full-time, or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including:

• Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers)
• 401(K)
• Paid time off (PTO)
• Employee recognition awards
• Multiple ERG’s (employee resource groups)

Pay

Commensurate with experience.

Schedule

Full-time, office-based position in Dallas, TX.