Clinical Business Analyst: Are you ready to take your clinical research career to the next level by joining a global leader in clinical trial technology? Clario, a pioneer in endpoint technology with over five decades of expertise, is seeking a Clinical Business Analyst to join its dynamic and forward-thinking global team. This is a remote opportunity, ideal for professionals who thrive in a collaborative yet independent working environment and have a deep understanding of clinical protocols and data management.
🏢 Company: Clario
📍 Location: Remote (India)
🎓 Education Required: B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc, or any Life Sciences discipline
📅 Experience Required: Minimum 2 years in Medical Writing, Clinical Data Management, Project Management, or Clinical Business Analysis
🔒 Verified Job Posting
About Clario:
Clario is a global innovator in clinical trial endpoint technology, offering cutting-edge solutions for data capture, medical imaging, diagnostics, and evidence generation. With a legacy of 50+ years, Clario accelerates drug development and enhances data accuracy to support faster market access for life-saving therapies. The company operates across therapeutic areas and is trusted by sponsors, CROs, and regulatory authorities worldwide.
Role Overview:
As a Clinical Business Analyst, you will act as the critical liaison between Clario’s Imaging Business Units, Medical & Scientific Affairs, Software Development, and Clinical Data Management teams. Your primary responsibility will be to translate complex clinical study protocols into clear, actionable software requirements, ensuring alignment with regulatory standards and organizational objectives.
Key Responsibilities:
📄 1. Requirements Gathering, Analysis & Documentation
- Comprehensively review and analyze clinical protocols, imaging charters, and compliance documentation.
- Translate these documents into software design requirements with precision and clarity.
- Collaborate cross-functionally with internal teams (Medical, Scientific, Regulatory, and Product) to ensure mutual understanding and alignment.
- Maintain version-controlled documentation and ensure timely updates based on stakeholder feedback.
⚙️ 2. Software Development Support & Validation
- Act as the point of contact for the software development team during the design, build, and deployment phases.
- Clarify requirements, resolve ambiguities, and ensure that deliverables meet intended functionality.
- Participate in User Acceptance Testing (UAT), help identify and resolve bugs, and support quality assurance initiatives before release.
🧠 3. Medical & Scientific Collaboration
- Provide clinical insight and technical input to the Medical & Scientific teams to ensure consistency across study documents and system configurations.
- Attend internal and external study-related meetings to gather software-specific needs and offer domain expertise.
📈 4. Product Enhancement & Project Management
- Collaborate with Product Management teams to recommend enhancements and new features based on real-world use cases and end-user feedback.
- Support Clinical Project Managers in monitoring project timelines, adjusting project scopes, and managing change controls effectively.
📊 5. Clinical Data Management Support
- Ensure consistency and accuracy in data capture tools, CRF design, database structures, and delivery specifications.
- Work closely with the data management team to facilitate query resolution and data mapping, ensuring seamless integration and study execution.
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Qualifications & Preferred Experience:
Educational Background:
- Bachelor’s or Master’s degree in Pharmacy (B.Pharm, M.Pharm, Pharm.D), Life Sciences, or related fields.
- Equivalent relevant experience (2+ years) may substitute for formal education in certain cases
Work Experience:
- Minimum of 2 years in roles such as Clinical Business Analyst, Medical Writer, Clinical Data Manager, or Clinical Project Manager.
- Prior involvement in clinical trials is highly preferred.
- Familiarity with medical imaging and imaging charters is an added advantage.
- Hands-on experience in software configuration specifications is highly desirable.
Skills & Competencies:
- Strong analytical thinking with a keen eye for detail.
- Excellent written and verbal communication skills in English.
- Proficient in tools like MS Office Suite, and preferably project management tools.
- Ability to multitask and manage shifting priorities in a fast-paced and deadline-driven environment.
- Strong interpersonal skills and a collaborative mindset.
What Clario Offers:
💰 Competitive Salary Package aligned with industry standards.
🏥 Private Health Insurance to support your medical needs.
🏡 Flexible Work Environment with remote working options across India.
🏖️ Attractive Paid Time Off (PTO) policies for work-life balance.
🚀 Learning & Development initiatives to foster professional growth and skill enhancement.
🎉 Employee Engagement Programs to keep you connected, motivated, and empowered.
How to Apply:
Ready to make a meaningful impact in clinical research with a leading global player?
💡 Early applications are encouraged as the position may close once the ideal candidate is found.
For a personalized resume, cover letter, or LinkedIn profile optimization tailored for this role or others in clinical research and pharmacovigilance, feel free to ask.