Discover rewarding pharma jobs in clinical data management. Join Clario’s remote team in Costa Rica for QC jobs ensuring trial data accuracy. Ideal for pharmaceutical careers with 1+ year experience. Apply now for this full-time role!
About the Company
Clario stands as a global leader in clinical trial data management, founded on over 50 years of expertise to transform lives by unlocking better evidence. With a mission to reduce disease and enhance patient outcomes, Clario delivers the richest clinical evidence through its innovative endpoint technology platform, supporting diverse trial models worldwide.
The company’s credibility shines through its role in over 700 FDA and EMA new drug approvals—accounting for 70% since 2015—and more than 30,000 clinical trials. Innovation drives Clario’s investments in science-informed technology, patient-centric operations, and advanced logistics across 100+ countries and languages.
Regulatory compliance is paramount, backed by robust global infrastructure, 24/7 support, and commitments to diversity, sustainability, and cybersecurity. As a growing powerhouse with revolutionary leadership, Clario fosters collaboration and meaningful impact, empowering professionals in pharmaceutical careers to accelerate life-changing therapies.
Job Details
- Company Name: Clario
- Experience: Minimum 1 year in pharmaceutical industry or related field
- Qualification: Bachelor’s degree preferred
- Location: Costa Rica Remote
- Work Type: Full-time / Remote
Job Description
Clario is expanding its Clinical Data Management team to support global clinical trials, seeking talented professionals for pharma jobs focused on data integrity and quality control. This role plays a vital part in reviewing clinical trial data, ensuring compliance and accuracy for high-impact studies.
As part of a collaborative environment, you’ll contribute to innovative processes that advance pharmaceutical research.
Associate Clinical Data Reviewer
- Department: Clinical Data Management
- Market: Global clinical studies
- Role: Perform data reviews, query issuance, and metrics generation for trial accuracy
- Experience: Minimum 1 year
- Education/Qualification: Bachelor’s degree preferred
Skills/Qualifications
- Strong problem-solving and organizational skills with high attention to detail
- Ability to manage multiple tasks and meet deadlines in fast-paced settings
- Excellent oral and written communication skills
- Fluency in English (verbal and written) required
- Familiarity with pharmaceutical industry processes and data management tools
- Proactive mindset for process improvements and team collaboration
Key Responsibilities
- Conduct manual data reviews for accuracy and completeness
- Issue queries per study-specific requirements
- Generate metrics and reports on database status
- Participate in project team meetings as needed
- Perform user acceptance testing (UAT) for systems
- Adhere to CDM processes, standards, and SOPs
- Collaborate to troubleshoot data issues
- Suggest efficiency-enhancing process improvements
- Assist team in meeting project deliverables
Benefits/Perks
- Competitive compensation packages
- Private health insurance coverage
- Flexible work schedules for better balance
- Attractive PTO plan with generous leave
- Engaging employee programs and events
- Flex workspace options in a remote setup
- Career growth through global projects and training
- Learning opportunities in cutting-edge clinical tech
- Positive work culture emphasizing innovation
- Global exposure to diverse pharma trials
How to Apply
To apply for this Associate Clinical Data Reviewer position, visit Clario’s official careers portal at https://clarioclinical.wd1.myworkdayjobs.com/en-US/clarioclinical_careers/job/Costa-Rica-Remote/Associate-Clinical-Data-Reviewer_R16304 and click the “Apply” button. Submit your resume, cover letter highlighting relevant pharma experience, and complete the requisition ID R16304 form.
Verified Post
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Why You Should Join
At Clario, you’ll immerse yourself in a vibrant company culture recognized for fostering inclusion, innovation, and employee well-being, where your contributions directly impact global health.
With long-term career stability backed by steady growth and a track record of supporting major drug approvals, this role offers security in the dynamic pharma landscape.
Embrace endless learning and growth opportunities through hands-on training, cross-functional projects, and exposure to advanced technologies in clinical research.
In a compliance-driven environment that prioritizes ethical practices and patient-centric innovation, you’ll thrive while making a tangible difference in bringing therapies to market faster. Join a team that’s not just changing data—it’s changing lives.
FAQs
What are the eligibility criteria for the Associate Clinical Data Reviewer role?
Candidates need a Bachelor’s degree (preferred), at least 1 year in pharma or related fields, English fluency, and strong organizational skills. Ideal for QC jobs in clinical data management.
How does the application process work for Clario pharma jobs?
Visit the careers page, search for requisition R16304, and submit your application online with resume and cover letter. Expect a review within 1-2 weeks, followed by interviews.
What growth opportunities are available in this position?
Clario offers training in data systems, project leadership paths, and global collaborations, supporting long-term advancement in pharmaceutical careers focused on clinical trials.
Is salary information provided for this QC job?
Compensation is competitive and based on experience; details discussed during interviews. Benefits include health insurance and flexible schedules for comprehensive rewards.