Bring your monitoring expertise to the forefront of innovation. We are looking for a Clinical Research Associate (CRA) Contractor 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
Duration: 6 months
FTE: 0.5 (20 hours per week)
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.
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.
- Location: Germany
- Therapeutic Areas: Oncology is a pre
- 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 Hungarian and English.
- Comfortable working independently and managing priorities.
- Willingness to travel throughout Hungary, as required.
- Effective clinical monitoring skills (all kind of visits mastered)
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.
“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-AdT #LI-remote
Skills Required
- Minimum 3–5 years of experience leading monitoring activities in complex clinical trials
- Strong understanding of ICH-GCP and regulatory guidelines
- Fluent communication in Hungarian and English
- Ability to work independently and manage priorities
- Willingness to travel throughout Hungary as required
- Effective clinical monitoring skills, including mastery of all visit types
- Experience in complex therapeutic areas such as cell and gene therapy or radiopharmaceuticals
What We Do
Allucent is on a mission to help bring new therapies to light by solving the distinct challenges of small and mid-sized biotech companies. The company is purpose-built through the convergence of leading providers to address this unmet need. Today, Allucent is a global provider of comprehensive drug development solutions, including consulting, clinical operations, biometrics and clinical pharmacology across a variety of therapeutic areas. With more than 30 years of experience in over 60 countries, Allucent’s individualized partnership approach provides experience-driven insights and expertise to assist its clients in successfully navigating the complexities of delivering novel treatments to patients.
