Principal Clinical Programmer (Rave/Veeva) - India (Home-Based)
Updated: March 26, 2025
Location: India-Asia Pacific - IND-Home-Based
Job ID: 25002054
Description
Principal Clinical Programmer (Rave + Custom Function/Veeva)
Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities.
Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.
Discover what our 29,000 employees, across 110 countries already know:
WORK HERE MATTERS EVERYWHERE
Why Syneos Health
We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards programs.
We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture unites us globally, and we are dedicated to taking care of our people.
We are continuously building the company we all want to work for and our customers want to work with.
Job Responsibilities:
Provides application administration and technical support as the subject matter expert on core business packages, including but not limited to: Medidata, Rave, Oracle OC/RDC, Oracle Inform, SAS, and supplemental packages.
Utilizes primary development tools and other supporting tools to design, write, validate, and maintain software to meet specifications.
Generates and maintains all required documentation, including specifications, coding, and validation efforts for annotated Case Report Forms (CRFs), database creation, coding setup, edit check procedures, import/export setup, listings, and custom reports.
Monitors applications proactively for workflow alerts, system errors, and performance issues, and troubleshoots programming deliverable defects.
Performs system integrations, application updates, and user acceptance testing.
Serves on project teams to coordinate and lead development activities for clinical programming projects, participates in discussions, and provides constructive feedback.
Keeps project teams informed of any issues that may impact project target dates, scope, or budget.
Reviews and provides input on study budgets, monitors project metrics, and manages scope of work.
Participates in bid defenses and provides input during project and departmental review meetings.
Ensures high-quality deliverables through senior review of program-level/multi-study core deliveries.
Attends sponsor audits and assists with in-progress audits.
Provides leadership, mentorship, training, and guidance to department members.
Manages project resources, proactively alerting management of delivery and resourcing needs.
Assists with vendor management and monitors service level agreements (SLAs).
Oversees the implementation of application upgrades and new modules from vendors.
Contributes to updating standard operating procedures and work instructions.
Qualifications:
Bachelor’s degree required, Master’s degree preferred. In lieu of a degree, equivalent related education and experience will be considered.
Must have experience with end-to-end clinical programming into Rave or Veeva EDC.
Ability to effectively engage with sponsors and internal customers at all levels.
Excellent written and verbal communication skills.
Demonstrated experience managing multiple priorities in a dynamic environment.
Experience working in a matrix-structured environment preferred.
Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint), email, and Voicemail.
Experience with programming languages such as PL/SQL, SAS, C#, or VB preferred.
Ability to travel as necessary (up to 25%).
Get to Know Syneos Health
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products, and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
No matter your role, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.
Additional Information:
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations when appropriate.
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China | Quarry Bay |Hubei :
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Zaventem |Bosnia and Herzegovina :
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Taipei |Williamson :
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