Clinical Research Associate

Allucent; United States; Remote; USD 85,000 - 110,000; Full time

Benefits offered by this job

Flexible hours

Remote / Hybrid

Mentoring

Training budget

Career progression

Buddy program

Referral program

Job summary

Allucent is seeking a Clinical Research Associate (CRA) to join our remote-capable team with travel across the United States. You will independently monitor investigational sites, ensure protocol adherence, and partner with investigators to maintain data integrity and patient safety.

As part of the A-team, you will mentor junior CRAs, drive issue resolution, and support ongoing site relationships. The role requires strong ICH-GCP knowledge, English fluency, and readiness to travel as needed.

Qualifications

• Experience leading monitoring activities in complex trials.
• Strong knowledge of ICH-GCP and regulatory guidelines.
• Excellent written and spoken English communication.
• Willingness to travel throughout the United States.

Responsibilities

• Independently manage monitoring of investigational sites across study phases.
• Ensure trial procedures comply with protocol, SOPs, and regulations.
• Maintain site relationships and data quality.
• Mentor junior CRAs and share best practices.
• Collaborate with sponsor and sites to ensure trial integrity and patient safety.

Skills

Site monitoring

Regulatory compliance

GCP knowledge

English communication

Travel readiness

Mentoring

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

Preferred location: West Coast, USA

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.

Requirements

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.

• Preferred Location: West Coast, 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

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 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

*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.