Clinical Research Associate

Allucent; Northern (KY); Hybrid; USD 70,000 - 110,000; Full time

Benefits offered by this job

Flexible working hours

Remote/hybrid options

Study/training budget

Buddy program

Job summary

Allucent is seeking a Clinical Research Associate (CRA) to independently monitor investigational sites, ensuring compliance with the trial protocol and GCP. The role is remote with travel across the United States, coordinating between sponsors and sites to maintain trial integrity.

You will lead monitoring activities, mentor junior CRAs, and manage site relationships to deliver high-quality data in oncology, cell & gene therapy, and neuroscience studies.

Qualifications

• 3–5 years of monitoring experience in clinical trials.
• Experience in complex therapeutic areas such as cell/gene therapy preferred.
• Strong knowledge of ICH-GCP and regulatory guidelines.
• Clear and confident communicator in English.

Responsibilities

• Independently manage all aspects of monitoring for assigned trials across study phases, including initiation, routine monitoring, and close-out visits.
• Ensure compliance with protocols, GCP, ICH, SOPs, and regulatory requirements.
• Build strong site relationships, acting as primary contact and ensuring high-quality data collection.
• Identify and resolve site issues, escalate as needed to maintain trial integrity and patient safety.
• Mentor and support junior CRAs, sharing knowledge and best practices.

Skills

CRA experience

English fluency

Independent worker

Travel willingness

Site monitoring

Job description

Bring your monitoring expertise to the forefront of innovation. We are looking for a Clinical Research Associate (CRA) to join our A-team (remote; with travel). As a CRA at Allucent, you will independently control and monitor investigational sites, pro-actively detect issues, provide solutions to ensure clinical studies are performed according to the trial protocol and in compliance with SOPs, applicable regulations, and the principles of Good Clinical Practice.

At Allucent™ we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe. At Allucent we are big enough to deliver and small enough to care. We know all our colleagues by name and work together as a team to make everyone SHINE.

The role

As a CRA, you will take the lead on monitoring activities, owning your sites and relationships with investigators. You’ll be the bridge between sponsor and site, ensuring trial integrity while being supported by a collaborative, experienced team. You will be a mentor for junior team members and contribute to grow our success. You will travel throughout the United States.

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

Main 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.

Who are we looking for

You’re an experienced CRA / monitor ready to take the next step with a company that truly values your expertise and independence. You thrive in an agile, collaborative environment and want to be part of a team making a real impact.

• Location: United States
• Therapeutic Areas: Oncology, Cell & Gene Therapy, and/or Neuroscience
• Experience leading monitoring activities in complex trials with a minimum of at least 3-5 years’ experience.
• Experience in complex therapeutic areas such as cell and gene therapy, radiopharmaceutical preferred.
• Strong understanding of ICH-GCP and regulatory guidelines.
• Clear and confident communicator in English.
• Comfortable working independently and managing priorities.
• Willingness to travel throughout the United States, as required.
• Effective clinical monitoring skills (all kind of visits mastered)

Benefits of working at Allucent include

• Comprehensive benefits package per location
• Competitive salaries per location
• Departmental Study/Training Budget for furthering professional development
• Flexible Working hours (within reason)
• Opportunity for remote/hybrid* working depending on locationLeadership 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

Disclaimers

*Our policy encourages a dynamic work environment, prescribing a minimum of 2 days in office per week for employees within reasonable distance from one of our global offices.

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