Sr Clinical Programmer (Dm Sas Expert)

5+ years

Not Disclosed

India

10 March 9, 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

Sr Clinical Programmer (DM SAS Expert)
Updated: March 5, 2025
Location: India-Asia Pacific - IND-Home-Based, India
Job ID: 24006735

Description:

Senior Clinical Programmer
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 about changing lives.

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 a total rewards program.
We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what 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. When we bring together diversity of thoughts, backgrounds, cultures, and perspectives, we create a place where everyone feels like they belong.

Job Responsibilities:

Utilizes primary development tools including Medidata, Rave, Oracle OC/RDC, Oracle Inform, and/or SAS to design, write, validate, and maintain software.
Generates and maintains documentation, including development specifications, programs, and validation efforts for annotated Case Report Forms (CRFs), database creation, coding configuration, and custom reports.
Coordinates and leads development activities for clinical programming projects, providing constructive feedback and keeping project management informed.
Provides technology support to clinical programming staff, project analysts, and data managers, assisting in coding, validation, and database creation.
Ensures high-quality deliverables through senior review of study-level and program-level core deliveries.
Reviews and provides input on study budgets and monitors the scope of work against actual work.
Performs system integration activities, application updates, and user acceptance testing.
Leads clinical programming activities on multiple concurrent studies, managing project resources and delivery needs.
Assists in project meetings and actively contributes to departmental review meetings.

Qualifications:

Minimum 5 years of experience in DM SAS Programming.
Strong hands-on experience in Advanced SAS and SAS macros.
Knowledge and experience with SQL.
Hands-on experience in developing SAS programs from scratch.
Experience in the DM domain.
Strong ability to deal effectively with sponsors and internal customers at all levels.
Excellent communication and interpersonal skills.
Experience managing multiple priorities in a highly dynamic environment.
Experience working in a matrix-structured environment is preferred.
Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint), email, and voicemail.

Get to Know Syneos Health:
Over the past five 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 what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment.

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 and job responsibilities. Equivalent experience, skills, and education will also be considered. The company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations when appropriate.

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