Clinical Research Associate
Allucent
Summary
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.
Job description
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)
Requirements
- 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
- Comprehensive Benefits Package
- Competitive Salary
- Professional Development Budget
- Flexible Working Hours
- Remote or Hybrid Working Options
- Leadership and Mentoring Opportunities
- Buddy Program
- Internal Growth and Career Progression
- Employee Referral Program
- Online Soft-Skills and Technical Training
- Spot Bonus Program
- Loyalty Award Program
Company overview
Allucent is a global, full-service contract research organization (CRO) dedicated to partnering with small and mid-size biopharmaceutical companies to advance innovative therapies through every phase of drug development. Founded in 2022 through the merger of several high-performance companies, Allucent combines over 30 years of collective experience in regulatory trends, therapeutic expertise, and operational excellence. The company specializes in oncology, neuroscience, and infectious diseases, with cross-therapeutic capabilities in rare diseases and advanced therapies like cell and gene therapy. With offices across North America, Europe, and the Middle East, Allucent has conducted trials in more than 60 countries, focusing on complex development areas that address unmet medical needs. The company's mission is to 'help bring new therapies to light' by providing comprehensive drug development solutions including clinical operations, regulatory strategy, clinical pharmacology, biometrics, and pharmacovigilance services. Allucent's individualized partnership approach and flexible regulatory solutions help biopharma clients accelerate development timelines, overcome complexity, and deliver life-changing treatments to patients worldwide.