Archive Specialist, Data Management

Posted 4 Days Ago
Be an Early Applicant
Bangalore, Bengaluru Urban, Karnataka, IND
In-Office
Mid level
Healthtech • Software
The Role
Manages final clinical trial archives after database lock, ensuring documentation is complete, organized, accurate, and compliant. Responsibilities include auditing records, coordinating document collection, building archive structures, supporting data generation, conducting quality reviews, packaging and delivering archives, tracking milestones, maintaining metrics, training stakeholders, and improving processes. The role collaborates with study teams, vendors, and internal partners across multiple studies while meeting closeout deadlines and regulatory requirements.
Summary Generated by Built In

Join Clario, a part of Thermo Fisher Scientific and help ensure the secure, accurate, and timely delivery of critical clinical trial documentation that supports global research programs. As an Archive Specialist within our Digital Physiology Data Management team, you will play a vital role in managing final study archives following database lock, ensuring study documentation is complete, organized, and compliant with customer and regulatory requirements. Working across multiple studies and collaborating with project teams throughout the organization, you will help drive operational excellence while supporting efficient study closeout activities and delivering an exceptional customer experience.

What We Offer

  • Competitive pay and incentives.

  • Provident fund and medical insurance.

  • Engaging employee programs and local events.

  • Modern office spaces and remote work flexibility.

What You'll Be Doing

  • Serve as the primary owner of post-database lock final archive deliverables for multiple studies simultaneously.

  • Identify, collect, verify, audit, and organize clinical trial documentation required for sponsor and site archives.

  • Conduct initial archive audits and assess documentation completeness following formal archive requests.

  • Create and maintain study-specific archive documentation and provide standard archive templates to project teams.

  • Build and manage complex archive directory structures for both site and sponsor archive packages.

  • Coordinate document acquisition activities and work closely with study teams to obtain outstanding closeout documentation.

  • Support data generation activities, including study design acquisition, environment setup, reporting activities, and documentation review.

  • Perform post-data generation processing activities and ensure archive contents meet quality and compliance requirements.

  • Execute quality reviews of archive packages and associated documentation prior to final delivery.

  • Prepare, package, upload, and coordinate delivery of completed archives through approved vendors and distribution channels.

  • Communicate archive priorities, status updates, and delivery timelines with project teams, vendors, and internal stakeholders.

  • Track archive shipments, coordinate delivery confirmations, and initiate archive decommissioning activities.

  • Perform quality checks on related archive deliverables and support cross-functional quality assurance activities.

  • Maintain archive metrics, dashboards, milestone trackers, and reporting tools on a daily, weekly, and monthly basis.

  • Support quarter-end archive planning activities to ensure delivery priorities align with business objectives and revenue targets.

  • Train and support team members and cross-functional partners on archive processes, documentation requirements, and best practices.

  • Participate in process improvement initiatives that enhance archive efficiency, documentation acquisition, and operational effectiveness.

What We Look For

  • Bachelor's degree preferred, or equivalent combination of education and relevant professional experience.

  • Minimum 2 to 5 years of Clinical Data Management, document management, records management, archives management, clinical operations, or related experience.

  • Strong understanding of clinical trial documentation, study lifecycle activities, and regulated environments preferred.

  • Demonstrated ability to independently manage projects and drive archive activities from initiation through completion.

  • Exceptional organizational skills with the ability to manage multiple priorities and competing deadlines simultaneously.

  • Experience working with document management systems, electronic trial master files, archive repositories, or related platforms is preferred.

  • Proficiency with Microsoft Office applications, Adobe Acrobat, and collaboration tools.

  • Strong attention to detail and commitment to quality, accuracy, and compliance.

  • Excellent verbal and written communication skills, including the ability to communicate effectively in English.

  • Proven ability to build relationships and collaborate effectively across departments and stakeholder groups.

  • Strong problem-solving skills with the ability to identify issues and drive timely resolution.

  • Ability to adapt quickly, shift priorities effectively, and perform successfully in deadline-driven environments.

  • Customer-focused mindset with demonstrated responsiveness and accountability.

At Clario, a part of Thermo Fisher Scientific, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.

Skills Required

  • Bachelor's degree or equivalent combination of education and relevant professional experience
  • 2 to 5 years of experience in clinical data management, document management, records management, archives management, clinical operations, or a related field
  • Understanding of clinical trial documentation, study lifecycle activities, and regulated environments
  • Ability to independently manage projects and archive activities from initiation through completion
  • Strong organizational skills and ability to manage multiple priorities and competing deadlines
  • Experience with document management systems, electronic trial master files, archive repositories, or related platforms
  • Proficiency with Microsoft Office applications, Adobe Acrobat, and collaboration tools
  • Strong attention to detail and commitment to quality, accuracy, and compliance
  • Excellent verbal and written communication skills, including effective communication in English
  • Ability to build relationships and collaborate across departments and stakeholder groups
  • Strong problem-solving skills and ability to drive timely issue resolution
  • Ability to adapt quickly and perform effectively in deadline-driven environments
  • Customer-focused mindset with responsiveness and accountability

Clario Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Clario and has not been reviewed or approved by Clario.

  • Leave & Time Off Breadth Time off is described as generous, including flexible PTO for some roles and up to 26–31 PTO days for eligible staff. The calendar includes 15 paid company holidays and a Winter Break.
  • Healthcare Strength Healthcare offerings include multiple medical plan options via Highmark with coordinated care navigation, plus dental and vision through established carriers. Employer HSA contributions and mental-health support broaden the package.
  • Inclusive Benefits Coverage Coverage highlights include domestic-partner eligibility, transgender-inclusive care, and HIV prevention/treatment. These inclusive elements are presented alongside broader inclusion commitments.

Clario Insights

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The Company
HQ: Philadelphia, NJ
6,733 Employees
Year Founded: 1972

What We Do

-- Clario has been named a Top Workplace by Energage for the 2022 Top Workplaces USA national awards. -- Clario generates the richest clinical evidence by fusing our deep scientific expertise and global scale into the broadest endpoint technology platform. By doing this, we empower our partners to transform lives. With almost 50 years of experience, 19,000 clinical trials, and 870 regulatory approvals, Clario has mastered the ability to generate rich evidence across a Trial Anywhere™ portfolio: decentralized (DCT), hybrid and site-based clinical trials. With 30 facilities in nine countries across North America, Europe, and Asia Pacific, Clario delivers the power of certainty. Partners ————— Clario brings the best of ERT and Bioclinica together to work alongside our partners to solve some of their biggest questions on topics such as: - eCOA vs. paper - Decentralized Clinical Trial (DCT) - Rescue a clinical trial - Broad endpoint technology: cardiac safety, imaging, respiratory And many more. People ———— We are so honoured to be named a 2022 Top Workplace by Energage. One of our leading values at Clario is People First Always. We help individuals build meaningful careers at Clario as they serve to help transform patients lives. Join us on this journey and check out our careers page: https://clario.com/careers/

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