Principal Clinical Programmer (Veeva)
Company: Syneos Health
Location: Hyderabad, Telangana, India
Work Mode: Hybrid
Employment Type: Full-Time
Job Overview
The Principal Clinical Programmer (Veeva) is a senior-level clinical data management and clinical programming professional responsible for end-to-end clinical database development, Veeva CDMS administration, EDC study setup, system integrations, programming oversight, vendor management, and leadership of multiple clinical studies. The role serves as a Subject Matter Expert (SME) for clinical programming platforms and provides technical leadership, mentorship, and strategic support across global clinical trials.
Key Responsibilities
Serve as Subject Matter Expert (SME) for Veeva CDMS, Medidata Rave, SAS, and other clinical programming applications.
Design, develop, validate, maintain, and support clinical programming solutions following standard development procedures.
Lead end-to-end clinical database build activities including eCRF design, edit checks, coding setup, imports, exports, listings, and reporting.
Generate and maintain all required study documentation, specifications, validation records, and programming deliverables.
Monitor systems for workflow alerts, performance issues, system errors, and troubleshoot technical defects.
Perform system integrations, application upgrades, User Acceptance Testing (UAT), and deployment activities.
Lead clinical programming activities across multiple concurrent studies and ensure timely project delivery.
Participate in sponsor meetings, project reviews, bid defenses, audits, and inspections.
Review study budgets, monitor project metrics, manage scope changes, and support change order processes.
Provide senior review of programming deliverables to ensure quality, compliance, and accuracy.
Manage application vendors, monitor service level agreements (SLAs), and support vendor escalations.
Supervise implementation of new system modules and software upgrades.
Contribute to SOP development, process improvements, and departmental best practices.
Mentor, train, and provide technical leadership to junior programmers and study teams.
Support resource planning and oversee clinical programming operations across multiple studies.
Required Qualifications
Bachelor's Degree in Life Sciences, Computer Science, Information Technology, Statistics, Pharmacy, Biotechnology, or a related discipline.
Master's Degree preferred.
Strong expertise in Veeva CDMS and clinical data management systems.
Extensive experience in EDC study setup and database configuration.
Strong knowledge of clinical trial processes and clinical data standards.
Experience with system integrations, validation, and clinical programming lifecycle activities.
Excellent communication, leadership, and stakeholder management skills.
Preferred Qualifications
Experience with Medidata Rave, SAS, and other clinical data management platforms.
Knowledge of CDISC standards and regulatory requirements.
Experience supporting sponsor audits and regulatory inspections.
Exposure to vendor management and service delivery oversight.
Experience managing global clinical studies and cross-functional teams.
Prior people management and mentoring experience.
Experience Required
8–9+ years of experience in Clinical Programming and Clinical Data Management.
Extensive hands-on experience with:
Veeva CDMS
EDC Study Setup
Database Build
eCRF Design & Configuration
Edit Check Programming
Post Go-Live Changes
Study Lock Activities
Clinical Trial Data Management
Uttar Pradesh :
Agra | Gajraula | Gautam buddha Nagar | Ghaziabad | Gorakhpur | Greater Noida | Jhansi | kanpur | Lucknow | Mathura | Noida | Park City | Prayagraj | Satyamev | Varanasi |Gujarat :
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Hajipur | Patna |Kerala :
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Ranchi |Sikkim :
Rangpo |India :
Remote, India | Siliguri |Illinois :
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Appleton | Kenosha | Pleasant Prairie | Portage | Waukesha |United states :
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Canada |Quebec :
Montreal |Brussels :
Brussels |Antwerp :
Heist op den Berg |Flemish Brabant :
Zaventem |South America :
Argentina | Peru |Brazil :
Sao paulo | Brazil |Attica :
Athens | Koropi |Greece :
Greece |North Island :
Auckland |New Zealand :
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Austria |Vienna :
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Madrid |Cebu Province :
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Manila |Croatia :
Croatia |Zagreb :
Zagreb |Estonia :
Estonia | Tartu |Harju County (Maakond) :
Tallinn |Hà Nội :
Hanoi | Hà Nội |Ho Chi Minh :
Ho Chi Minh City |Italy :
Italy |Lombardy :
Rho |Jakarta :
Jakarta |East Java :
Surabaya |Japan :
Saitama | Japan |Tokyo :
Otemachi |North Ostrobothnia :
Oulu |Southwest Finland (Varsinais-Suomi) :
Turku |Remote Korea :
Remote Korea |Republic of Korea :
Seoul |Kazakhstan :
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Bangkok |Israel :
Be'Er Sheva | Tel Aviv | Netanya | Yavne | Kfar Saba |Remote :
Belgium | Perth | Leinster | Regulatory Labeling Manager (NA and LATAM Only) | Springville | Minnesota | Bountiful | Lousiana | Remote - Africa | Remote - Middle East | Faridabad | Xzagreb | Hungary | Medan | Slovakia | Remote - South America (Latin Americal) | Hammond | Victoria | Green Way | Nairobi | Lenexa | Switzerland | French | Castlebar | Ireland | Riga | Remote - Europe | Texas | Bishop | Blue Bell | Melbourne | Zaragoza | McFarland | Tulsa | Milwaukee | Manipal | Thailand |Republic of Colombia :
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New Mexico | Ciudad de México |Dubai :
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Kyiv |Lima Region :
Lima |France :
Lyon | Paris |South Africa :
South Africa | Midrand |Nišava District :
Niš |Bohemia :
Prague |Chile :
Santiago |Bosnia and Herzegovina :
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Singapore |Sofia City :
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Sweden |Taipei :
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