Clinical Research Associate

Allucent; United States; Hybrid; USD 70,000 - 90,000; Full time

Benefits offered by this job

Comprehensive benefits

Competitive salaries

Flexible working hours

Professional development budget

Internal growth opportunities

Job summary

Allucent is seeking a Clinical Research Associate (CRA) with expertise in clinical monitoring to join their team remotely. The CRA will independently manage monitoring activities, ensuring compliance with study protocols and maintaining strong relationships with investigational sites.

The ideal candidate has at least 3-5 years of experience, particularly in complex therapeutic areas such as oncology and gene therapy.

Qualifications

• Minimum of 3-5 years’ experience in clinical research.
• Strong understanding of ICH-GCP and regulatory guidelines.
• Experience in cell and gene therapy is preferred.

Responsibilities

• Independently manage monitoring for assigned trials.
• Ensure compliance with protocols and regulatory requirements.
• Build strong relationships with study sites.

Skills

Clinical monitoring

Communication

Problem-solving

Regulatory knowledge

Team collaboration

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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