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Post: Clinical Programmer II - SAS (India)
Job Description
- Utilizes primary development tools including Oracle RDC, Oracle Inform, Medidata Rave, Omnicomm TrialMaster, SAS, NCG CRF WorkManager, 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 setup, edit check procedures, import setup and processing, export setup and processing, listings, and profile reporting.
- 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 criticism. 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.
- Monitors the scope of work to actual work, alerting management of potential change orders. Manages and executes the change order to completion. Provides input and supporting details for 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.
Candidate profile
Bachelor Degree in Science or health care field.
Experience in clinical data management in a CRO setting with SAS programming proficiency.
Strong organizational, documentation, and interpersonal skills as well as a willingness to work within a team-oriented environment.
Ability to handle multiple tasks to meet deadlines in a dynamic environment.
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.
Additional Information:
Qualification: Any science graduate
Industry Type: Pharma/ Biotech/Clinical Research
End Date: 15th August, 2014
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