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Clinovo Hiring remote Clinical Data Managers and Programmers

Clinovo hiring remote Clinical Data Managers and Programmers in India with Veeva Vault CDMS experience for global CRO roles.


About Clinovo

Clinovo is a global digital-focused Clinical Research Organization (CRO) that combines data, technology, and operational excellence to support sponsors across the world. The organization specializes in modern clinical data solutions, using advanced platforms like Veeva Vault CDMS to streamline data collection, cleaning, monitoring, and reporting. Clinovo Hiring remote Clinical Data Managers and Programmers

With a strong emphasis on remote collaboration, process automation, and compliance with global standards such as GCP and CDISC, Clinovo provides an excellent environment for experienced Clinical Data Management and Programming professionals who want to work with cutting-edge tools while enjoying flexible work-from-home opportunities within India. Clinovo Hiring remote Clinical Data Managers and Programmers

Currently, Clinovo is inviting applications from experienced professionals for the roles of Clinical Data Manager and Clinical Programmer with strong hands-on expertise in Veeva Vault CDMS and other Veeva tools. These are fully remote positions for candidates based in India, with a preference for immediate joiners. Clinovo Hiring remote Clinical Data Managers and Programmers


Key Highlights

ParticularsDetails
CompanyClinovo
RoleClinical Data Manager & Clinical Programmer
Technology FocusVeeva Vault CDMS and Veeva tools
LocationRemote, India
Experience Required2 to 8 years
EducationB.Pharm, M.Pharm, Pharm.D, MSc, BSc, Life Sciences, CS
Job TypeFull-time, Remote
IndustryClinical Research / Digital CRO / Clinical Data Management
Application ModeEmail
Published On10 December 2025
Immediate JoinersHighly Preferred

Role Overview

Clinovo is hiring experienced Clinical Data Managers and Clinical Programmers who are adept at working with Veeva Vault CDMS. These roles are designed for professionals who already have hands-on experience in managing clinical trial data and programming within Veeva-based environments. Clinovo Hiring remote Clinical Data Managers and Programmers

As part of a global digital CRO, you will be supporting clinical studies for international pharmaceutical and biotech clients. The roles demand a strong understanding of clinical data standards, regulatory expectations, and the ability to collaborate seamlessly in a fully remote setup.

You will work across multiple phases of clinical trial data management and programming, from study design to database lock, ensuring high levels of data quality, compliance, and efficiency. Clinovo Hiring remote Clinical Data Managers and Programmers

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Responsibilities – Clinical Data Manager

As a Clinical Data Manager working on Veeva Vault CDMS, your key responsibilities will include:

1. End-to-End Clinical Data Management

You will manage clinical data activities right from study setup to database lock. This involves coordinating with cross-functional stakeholders and ensuring that all data management tasks follow protocol requirements and sponsor expectations.

2. Veeva Vault CDMS Study Setup and Configuration

You will be involved in:

  • Study build and configuration in Veeva Vault CDMS
  • User Acceptance Testing (UAT) of the database
  • Managing mid-study updates and amendments
  • Ensuring database readiness before subject enrollment and major milestones

3. Data Review and Query Management

You will perform thorough data review to identify inconsistent, missing, or discrepant data. Your day-to-day tasks will include:

  • Generating, reviewing, and resolving data queries
  • Communicating with clinical operations teams for query resolution
  • Ensuring timely closure of discrepancies to keep database clean and audit-ready

4. Compliance and Standards

You will ensure that all DM activities comply with:

  • Good Clinical Practice (GCP) guidelines
  • CDISC and other relevant data standards
  • Internal SOPs, sponsor requirements, and regulatory expectations

5. Cross-Functional Collaboration

You will collaborate with biostatistics, clinical operations, programming, and project management teams to ensure that timelines and quality expectations are consistently met. Being in a remote environment, strong communication and documentation are essential.


Responsibilities – Clinical Programmer

As a Clinical Programmer with Veeva Vault CDMS experience, you will work on technical configuration, edit checks, listings, and data extraction programming. Clinovo Hiring remote Clinical Data Managers and Programmers

1. Edit Check and Listing Development

You will develop and validate:

  • Edit checks to identify inconsistent or incorrect data
  • System checks for automatic issue detection
  • Custom listings and data views to support data review and monitoring

Your programming work will support efficient data cleaning and faster decision-making.

2. Database Design and Build Support

You will participate in:

  • Designing database structures in Veeva Vault CDMS
  • Supporting build and unit testing activities
  • Implementing changes requested during UAT or protocol amendments
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Your role ensures that the technical setup of the EDC system aligns with protocol requirements and data flow expectations. Clinovo Hiring remote Clinical Data Managers and Programmers

3. Automated Program Development

You will create and validate automated programs to:

  • Extract data from the Veeva CDMS environment
  • Generate data transfer files and listings
  • Support downstream analysis and review processes

4. Troubleshooting and Technical Support

You will troubleshoot system-related issues, performance concerns, and programming errors related to CDM systems. This includes working closely with internal IT or platform support teams whenever necessary.

5. Timely Delivery of Outputs

You will be responsible for delivering high-quality programming outputs within the defined timelines. This includes managing priorities, communicating risks, and ensuring your tasks align with project schedules.


Required Qualifications and Background

To be eligible for these roles, candidates should have: Clinovo Hiring remote Clinical Data Managers and Programmers

  • Strong hands-on experience with Veeva Vault CDMS or other Veeva tools (mandatory)
  • Background in Clinical Data Management or Clinical Programming
  • Experience range between 2 to 8 years in clinical research or CRO environments

Educational Qualifications

Candidates should hold a degree in one of the following:

  • B.Pharm or M.Pharm
  • Pharm.D
  • BSc or MSc (Life Sciences or related)
  • BSc / MSc in Computer Science
  • Other relevant degrees in Lifesciences or Clinical Research

Skills and Competencies

To excel in these roles, you should possess: Clinovo Hiring remote Clinical Data Managers and Programmers

  • Demonstrated experience working on Veeva Vault CDMS
  • Strong understanding of clinical trial processes and data flow
  • Good knowledge of data standards such as CDISC (preferred for DM roles)
  • Excellent communication skills for working in a remote setup
  • Strong analytical and problem-solving abilities
  • Ability to collaborate with global teams and work independently
  • Comfort with remote tools, virtual meetings, and online project management systems

Work Environment and Benefits

These positions are entirely remote within India, providing flexibility and convenience while still working on global projects. Clinovo Hiring remote Clinical Data Managers and Programmers

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Key Benefits

  • 100% remote work setup
  • Opportunity to work on international clinical studies
  • Exposure to modern digital and Veeva-based workflows
  • Collaboration with global clinical, data, and programming experts
  • Career growth in a specialized, high-demand niche (Veeva CDMS)

Working with Clinovo gives you the chance to stay at the forefront of clinical technology and data-driven research while enjoying location flexibility. Clinovo Hiring remote Clinical Data Managers and Programmers


Who Should Apply

These roles are ideal for:

  • Clinical Data Managers seeking to specialize in Veeva Vault CDMS
  • SAS or CDM Programmers looking to transition into or deepen their Veeva experience
  • Clinical research professionals with 2 to 8 years of experience who are comfortable working in a fully remote environment
  • Professionals who can join immediately or within a short notice period
  • Candidates who enjoy working with technology platforms and solving complex data problems

If you are passionate about clinical data, digital transformation, and remote teamwork, these roles can significantly accelerate your career. Clinovo Hiring remote Clinical Data Managers and Programmers


How to Apply

Interested and eligible candidates can apply through email application.

Follow the steps below to submit your application: Clinovo Hiring remote Clinical Data Managers and Programmers

  1. Update your CV highlighting:
    • Your experience in Veeva Vault CDMS
    • Clinical Data Management or Clinical Programming responsibilities
    • Types of studies and phases you have worked on
    • Any experience with global sponsors or CROs
  2. Use a clear subject line such as:
    Application for Clinical Data Manager – Veeva CDMS (Remote, India)
    or
    Application for Clinical Programmer – Veeva CDMS (Remote, India)
  3. Attach your latest resume in PDF or Word format.
  4. Send your email to the official Clinovo recruitment contact: Email ID: bhavanasri.gundala@clinovo.com
  5. In the body of the email, briefly mention:
    • Your total years of experience
    • Relevant Veeva Vault CDMS projects
    • Current location in India
    • Current CTC and expected CTC
    • Notice period or availability (mention if you are an immediate joiner)

Submitting a clear, well-structured application will increase your chances of being shortlisted for further discussion and interview rounds. Clinovo Hiring remote Clinical Data Managers and Programmers

For verified pharma job updates, visit PharmaJobHub.in – India’s trusted pharma career portal.

Note: This job information is sourced from publicly available official sources. We share it for reference purposes only and do not claim ownership of the job posting.

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