Clinical Research Associate

Allucent is a biopharmaceutical clinical research organization that helps small and medium-sized biopharmaceutical companies navigate clinical trials. The Clinical Research Associate will independently manage monitoring activities, maintain site relationships, ensure protocol and regulatory compliance, resolve site issues, and mentor junior CRAs while traveling throughout the United States.

Responsibilities

Independently manage all aspects of monitoring for assigned clinical trials across study phases, including site initiation, routine monitoring, and close-out visits

Ensure compliance with protocols, GCP, ICH, SOPs, and applicable regulatory requirements

Build strong site relationships, acting as a primary point of contact and ensuring high-quality data collection

Identify and resolve site issues, escalating as needed to maintain trial integrity and patient safety

Mentor and support junior CRAs, sharing knowledge and best practices

Preferred

Therapeutic Areas:Oncology, Cell & Gene Therapy, and/or Neuroscience

Experience in complex therapeutic areas such as cell and gene therapy, radiopharmaceutical preferred

Oncology

Gene Therapy

Neuroscience

Radiopharmaceuticals

Benefits

Comprehensive benefits package per location

Departmental Study/Training Budget for furthering professional development

Flexible Working hours (within reason)

Opportunity for remote/hybrid working depending on location

Leadership and mentoring opportunities

Participation in our enriching Buddy Program as a new or existing employee

Internal growth opportunities and career progression

Financially rewarding internal employee referral program

Access to online soft-skills and technical training via internal platforms

Eligibility for our Spot Bonus Award Program in recognition of going above and beyond on projects

Eligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employees

Company

Full-service CRO for biotech drug development and clinical trials

Cary, North Carolina, USA

https://www.allucent.com/

Founded in 1988

1001-5000 employees

Qualifications

Experience leading monitoring activities in complex trials with a minimum of at least 3-5 years' experience

Strong understanding of ICH-GCP and regulatory guidelines

Clear and confident communicator in English

Comfortable working independently and managing priorities

Effective clinical monitoring skills (all kind of visits mastered)

Therapeutic Areas:Oncology, Cell & Gene Therapy, and/or Neuroscience

Experience in complex therapeutic areas such as cell and gene therapy, radiopharmaceutical preferred

Experience leading monitoring activities in complex trials with a minimum of at least 3-5 years’ experience.

Required skills

Clinical Monitoring, ICH-GCP, Regulatory Guidelines, Oncology, Cell and Gene Therapy, Neuroscience, Radiopharmaceuticals

Experience

3-5 years