
Clinical Research Associate II / Sr. Clinical Research Associate
Allucent
full-time
Posted on:
Location Type: Remote
Location: Brazil
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About the role
- **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 Brazil.
- **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.
- - Location: Brazil
- - Experience leading monitoring activities in complex trials with a minimum of at least 3-5 years’ experience.
- - Experience in complex therapeutic areas such as oncology (solid and/or liquid), rare disease, and/or cell and gene therapy.
- - Strong understanding of ICH-GCP and regulatory guidelines.
- - Clear and confident communicator in English.
- - Comfortable working independently and managing priorities.
- - Willingness to travel throughout Brazil, 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
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
clinical trial monitoringsite initiationroutine monitoringclose-out visitsdata collectionregulatory complianceGCPICHSOPsclinical monitoring
Soft skills
leadershipmentoringcommunicationproblem-solvingindependencecollaborationrelationship buildingagilityprioritizationconfident communication