{bc}
Apply
workday

Clinical Programmer II (DMSAS)

Syneos Health
Hyderabad, IND
Full-time
Mid · 5+ years experience
Hybrid
Discovered Today
sas

Full Job Posting

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
  • 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
  • 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 what your role is, 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.
  • http://www.syneoshealth.com
  • 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 in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

Qualifications

  • 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
  • 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 what your role is, 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.
  • http://www.syneoshealth.com
  • 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 in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

Preferred Qualifications

  • Bachelor’s degree preferred, or equivalent combination of related education and experience.
  • Preferred Base and Advanced SAS certification

Apply for this job in 1 click

Skip the repetitive application forms

Install the Base Career Chrome Extension and autofill job applications across major job boards with your profile.

Sarah M.James T.Maya R.

Trusted by over 500,000 job seekers on Base Career

Start Free Today

More from this employer

More jobs at Syneos Health

Sr CRA I/ II (Melbourne/ Perth)- FSP

, AUS

Discovered TodayFull-time

CRA II / Snr CRA I - Multi Sponsor

, GBR

Discovered TodayFull-time

Sponsor dedicated - Sr Clinical Trial Supplies Associate - Client Office Hybrid Based (NY or NJ)

, USA

Discovered TodayFull-time

Sr Global Feasibility Lead - Sponsor dedicated (UK, Poland, Spain or US)

, GBR

Discovered 3 days agoFull-time

Médecin - Ville de Québec

Québec, CAN

Discovered 3 days agoPart-time

Sponsor Dedicated - Sr. Principal Medical Writer - Regulatory Submission Docs (ISE/ISS/Clinical Overview - Must Have)

, USA

Discovered 3 days agoFull-time

eTMF System Manager

Hyderabad, IND

Discovered 3 days agoFull-time

Sr Site Activation Manager

, USA

Discovered 3 days agoFull-time