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Clinical Programmer Ii

2+ years
Not Disclosed
10 April 30, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Clinical Programmer II (Rave/Veeva)
Updated: March 27, 2025
Location: India-Asia Pacific – IND-Home-Based
Job ID: 24006566

Job Description:
Syneos Health® is a fully integrated biopharmaceutical solutions organization dedicated to accelerating customer success. We provide clinical, medical, and commercial insights to address modern market realities, with a focus on bringing the customer and the patient to the center of everything we do. We are committed to simplifying and streamlining our processes, making Syneos Health easier to work with and for.

As a Clinical Programmer II, you’ll be part of a dynamic and collaborative team, leveraging your technical expertise to accelerate the delivery of therapies and ultimately change lives.

Why Join Syneos Health:

  • Career development and progression

  • Supportive and engaged line management

  • Technical and therapeutic area training

  • Peer recognition and total rewards programs

  • A culture that values authenticity and diversity

Key Responsibilities:

  • Utilize primary development tools (e.g., Oracle RDC, Oracle Inform, Medidata, Rave, SAS) to design, write, validate, and maintain software to meet project specifications

  • Develop and maintain documentation, including specifications, coding, and validation for annotated Case Report Forms (CRFs), database creation, edit check procedures, listings, and custom reports

  • Lead and coordinate development activities for clinical programming projects, ensuring project milestones are met

  • Monitor project scope, target dates, and budgets, escalating any potential risks or delays

  • Ensure quality deliverables by reviewing study level core deliveries for accuracy

  • Attend sponsor audits and assist with in-progress audits

  • Provide leadership, training, and support to junior programming team members

  • Manage project resources, proactively identifying resourcing needs

  • Attend Quick Start Camps (QSCs) and lead clinical programming activities on up to 8 concurrent studies

  • Maintain a broad knowledge of clinical programming and data management through ongoing self-training and professional development

Qualifications:

  • Bachelor’s degree preferred, or equivalent related education and experience

  • Strong communication and interpersonal skills, both written and verbal

  • Experience managing multiple priorities in a dynamic environment

  • Experience with programming languages like PL/SQL, SAS, C#, or VB preferred

  • Ability to travel as necessary (up to 25%)

About Syneos Health:

  • Worked with 94% of all Novel FDA Approved Drugs in the past 5 years

  • Supported 95% of EMA Authorized Products

  • Involved in 200+ studies across 73,000 sites and 675,000+ trial patients

Additional Information:
The company reserves the right to assign additional duties and responsibilities as needed. Qualifications may differ depending on experience, and the company is committed to compliance with all applicable federal and international employment laws.