Quick Summary
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,
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 environm
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.
Responsibilities
~1 min read- → 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.
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)
What We Offer
~1 min read*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.
“The Allucent Talent Acquisition team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively “Allucent”). Allucent does not accept unsolicited resumes from third-party recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third-party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources.”
#LI-TCW #LI-remote
Location & Eligibility
Listing Details
- Posted
- August 6, 2026
- First seen
- August 12, 2026
- Last seen
- August 12, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 46%
- Scored at
- August 12, 2026
Signal breakdown

Allucent is a global clinical research organization (CRO) dedicated to helping small and mid-sized biotech companies bring new therapies to light by providing comprehensive drug development solutions, including consulting, clinical operations, biometrics, and clinical pharmacology.
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