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Clinical Programmer Ii (Veeva/Inform/Rave)

2-6 years
Not Disclosed
10 Nov. 29, 2024
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

Company: Syneos Health
Location: Global


About Syneos Health

Syneos Health is a premier, fully integrated biopharmaceutical solutions organization focused on accelerating customer success. By leveraging deep clinical, medical, and commercial expertise, Syneos Health is dedicated to simplifying the clinical development process, ultimately transforming patient outcomes and accelerating the delivery of therapies.

"Work Here Matters Everywhere"


Why Syneos Health?

At Syneos Health, we are passionate about developing our people and fostering career progression. We offer technical training, peer recognition, and comprehensive rewards programs. Our Total Self culture encourages individuals to bring their authentic selves to work, fostering an inclusive and diverse environment where everyone belongs.

We are continuously building the company that our employees want to work for and our customers want to collaborate with.


Role Overview

The Clinical Programmer II will utilize various development tools, including Oracle RDC, Oracle Inform, Medidata, Rave, and SAS, to design, write, validate, and maintain software solutions for clinical studies. This role involves collaborating with cross-functional teams to ensure the accuracy and timeliness of clinical programming deliverables.


Key Responsibilities

  • Clinical Programming & Documentation:

    • Use Oracle RDC, Medidata, SAS, and other relevant tools to design, write, validate, and maintain software solutions.

    • Develop and maintain study documentation, including Case Report Forms (CRFs), database creation, coding configuration, edit check procedures, import/export setups, and custom reports.

  • Project Leadership & Coordination:

    • Serve as a key member of project teams, managing programming activities across up to eight concurrent studies.

    • Participate in project meetings, using an analytical approach to problem-solving and focusing on delivering results.

    • Provide updates on project milestones, issues, and potential delays to management, ensuring timely escalation of problems.

    • Ensure quality through reviewing study-level deliverables for accuracy and assisting with audits.

  • Cross-Functional Collaboration & Support:

    • Provide leadership, training, and guidance to team members.

    • Collaborate with clients, lead programmers, and project teams to clarify specifications and address evolving project needs.

    • Actively contribute to project and departmental review meetings.

  • Resource & Budget Management:

    • Review study budgets and scope, alerting management to potential changes or scope adjustments.

    • Proactively manage project resources, alerting management to delivery or resource needs.

  • Knowledge Sharing & Continuous Learning:

    • Keep up-to-date with developments in clinical programming and clinical data management.

    • Attend relevant training sessions, professional meetings, and engage in self-directed learning.


Qualifications

Education & Experience:

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

  • 2 to 6 years of experience in clinical programming with a focus on InForm, Rave, or Veeva (experience with eCRF design and programming required).

  • Proficiency in edit check programming for EDC systems (e.g., Inform Central Designer) is required.

  • Experience in clinical data management (DM domain) is essential.

Technical Skills:

  • SAS programming experience required (Advanced SAS knowledge is essential).

  • Experience with PL/SQL, C#, or VB is a plus.

  • Proficiency with Microsoft Office Suite (Word, Excel, PowerPoint).

Soft Skills:

  • Strong communication skills, both written and verbal.

  • Ability to manage multiple priorities in a dynamic environment.

  • Leadership and interpersonal skills to effectively collaborate in a matrix-structured environment.

  • Project management experience is a plus.

Other Requirements:

  • Ability to travel up to 25% as required.


Why Work with Us?

  • Career Growth: We invest in the continuous development of our people, offering a clear path for career progression and leadership opportunities.

  • Impact: Contribute to clinical programming that directly influences the advancement of new therapies.

  • Inclusive Environment: Join a team that values diversity and fosters collaboration across global teams.

  • Comprehensive Benefits: Competitive salary, health insurance, 401k match, flexible paid time off, and more.


Apply Now to join Syneos Health and be part of an innovative team that’s helping shape the future of healthcare.


At Syneos Health, we are committed to diversity and inclusion. We encourage candidates from diverse backgrounds to apply, even if their experience doesn’t perfectly match the qualifications. We value transferable skills and invite you to join our Talent Network for future opportunities.