Clinical Programmer II (DMSAS)

Syneos Health; India; On-site; INR 900,000 - 1,700,000; Full time

Job summary

Syneos Health, Inc. in India is seeking a Clinical Programmer II (DMSAS) to design, validate, and maintain clinical programming solutions using Oracle RDC, Oracle Inform, Medidata, Rave, and SAS.

You will generate study documentation, support lead programmers, attend sponsor audits, and manage multiple studies concurrently, ensuring high-quality deliverables and compliance. The role offers collaboration across teams in a fast-paced, patient-focused environment with opportunities for growth

Qualifications

• Bachelor's degree preferred, or equivalent combination of related education and experience.
• Must have minimum 2 to 4+years of experience in Clinical Programming
• DM SAS Listings and understanding the specifications
• Experience in perform the QC or VCP of the Listings
• Ability to understand the SAS macros
• Support Lead Programmers
• Strong Data Management (DM) SAS experience
• Preferred Base and Advanced SAS certification

Responsibilities

• Utilizes primary development tools including Oracle RDC, Oracle Inform, Medidata, Rave, SAS, and other supporting tools to design, write, validate, and maintain software to meet specifications in a timely and productive manner following standard development procedures.
• Generates and maintains all required documentation, including the development of specifications, coding, and validation efforts in support of annotated Case Report Forms (CRFs), database creation, coding configuration, edit check procedures, import setup and processing, export setup and processing, listings, and custom reports.
• Serves on project teams to coordinate and lead development activities for clinical programming projects. Attends meetings, participates in discussions, uses an analytical approach to problem solving, focuses on deliverables, and provides constructive feedback. Keeps those responsible for project management informed of any issues that might impact project target dates, scope, or budget and escalates potential problems effectively and in a timely manner. Balances multiple task assignments and communicates needs to supervisor to obtain needed resources.
• Ensures quality deliverables by providing review of study level core deliveries for accuracy. Attends sponsor audits and assists with in-progress audits.
• Reviews and provide input on study budgets and monitors scope of work to actual work, alerting management of potential change orders.
• Provides leadership, training, guidance, and support to other department members based upon expertise in specific skill sets. Collaborates with clients, peers, lead programmers, project teams and/or requestors to clarify and finalize specifications, and uses expanded technical skills to meet evolving project needs.
• Assists in project review meetings and assists with departmental review meetings.
• Attends Quick Start Camps (QSCs) as the lead clinical programmer for assigned studies.
• Leads clinical programming activities on up to eight (8) concurrent studies depending upon scope, similarity, program, and resourcing requirements.
• Manages project resources, proactively alerting management of delivery and resourcing needs.
• Possesses and maintains a broad overall knowledge in the field of clinical programming and clinical data management by reading related literature, self-training, attending training classes, attending professional meetings, etc.

Skills

Data Management SAS experience

SAS macros understanding

Lead programmer support

QC/VCP for listings

Clinical programming experience

Education

Bachelor's degree or equivalent

Related education/experience

Tools

Oracle RDC

Oracle Inform

Medidata

Rave

SAS

Job description

Clinical Programmer II (DMSAS) Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.

Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.

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 deliver - for one another, our customers, and, most importantly, for those in need.

Discover what your 25,000 future colleagues already know:

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 program.
• We are committed to building an inclusive culture - where you can authentically be yourself. Central to this is our purpose - Driven to Deliver - which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone's life.
• We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.

Job Responsibilities

• Utilizes primary development tools including Oracle RDC, Oracle Inform, Medidata, Rave, SAS, and other supporting tools to design, write, validate, and maintain software to meet specifications in a timely and productive manner following standard development procedures.
• Generates and maintains all required documentation, including the development of specifications, coding, and validation efforts in support of annotated Case Report Forms (CRFs), database creation, coding configuration, edit check procedures, import setup and processing, export setup and processing, listings, and custom reports.
• Serves on project teams to coordinate and lead development activities for clinical programming projects. Attends meetings, participates in discussions, uses an analytical approach to problem solving, focuses on deliverables, and provides constructive feedback. Keeps those responsible for project management informed of any issues that might impact project target dates, scope, or budget and escalates potential problems effectively and in a timely manner. Balances multiple task assignments and communicates needs to supervisor to obtain needed resources.
• Ensures quality deliverables by providing review of study level core deliveries for accuracy. Attends sponsor audits and assists with in-progress audits.
• Reviews and provide input on study budgets and monitors scope of work to actual work, alerting management of potential change orders.
• Provides leadership, training, guidance, and support to other department members based upon expertise in specific skill sets. Collaborates with clients, peers, lead programmers, project teams and/or requestors to clarify and finalize specifications, and uses expanded technical skills to meet evolving project needs.
• Assists in project review meetings and assists with departmental review meetings.
• Attends Quick Start Camps (QSCs) as the lead clinical programmer for assigned studies.
• Leads clinical programming activities on up to eight (8) concurrent studies depending upon scope, similarity, program, and resourcing requirements.
• Manages project resources, proactively alerting management of delivery and resourcing needs.
• Possesses and maintains a broad overall knowledge in the field of clinical programming and clinical data management by reading related literature, self-training, attending training classes, attending professional meetings, etc.

Qualifications

• Bachelor's degree preferred, or equivalent combination of related education and experience.
• Must have minimum 2 to 4+years of experience in Clinical Programming
• DM SAS Listings and understanding the specifications
• undefined
• Experience in perform the QC or VCP of the Listings.
• Ability to understand the SAS macros
• Support Lead Programmers
• Strong Data Management (DM) SAS experience
• Preferred Base and Advanced SAS certification

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 what your role is, you'll take the initiative and challenge the status quo with us in a highly competitive and ever-changing enviro