Login for faster access to the best deals. Click here if you don't have an account.

Senior Clinical Database Programmer Full-time Job

Nov 30th, -0001 at 00:00   IT & Telecoms   Pune   14 views Reference: 193
Job Details

Senior Clinical Database Programmer

#lifesciencegraduate #nagpurjobs #apportunities #clinicalresearchinstitute #smo #clinicalresearchcareers #clinicalresearchtrials #medicalresearch #healthcare #biology #pharmacovigilance #clinicalresearchtraining #education #bpharma #research #clinicalresearchers #nurse #clinicalresearchjobs #crc #pharmaceuticals #pharma #clinicaltrialsguru #clinicaldatamanagement #cralife #sciences #pharmacy #training #careers #rn #clinicaltrialsday The Senior Database Programmer provides technical expertise for the conduct of clinical trials, might act as an internal subject matter expert in specific areas providing technical support and expert advice, and works independently to support various programming activities related to clinical systems, and/or the applications/systems within eClinical technologies. In addition, the Senior Database Programmer can assist the Database Primary or Technical Lead role on projects, and liaise with sponsors, Data Management Lead and other functional areas as required. General areas of responsibility also includes: eCRF design, edit check programming and integration of third-party systems with the EDC databases. All tasks should be performed in accordance to corporate quality standards, SOPs/Work Instructions/Guidelines, ICH-GCP and/or other international regulatory requirements. Lead and supervise and/or create, implement and execute procedures to build and maintain database set-up for paper based and/or web based (EDC) clinical data management systems (CDMS) in standard format or CDISC compliant format as required, including the annotation of CRFs where applicable. Lead and supervise and/or create, implement and maintain consistency checks in standard or CDISC format for database builds in CDMS and EDC, following and understanding internal and external regulatory requirements. Accountable for first time quality on all deliverables. Strong ability to lead and collaborate with global teams and work independently. Motivate/guide virtual teams across multiple time zones and cultures to work effectively Strong interpersonal, oral and written communication skills using concise phrasing tailored for the audience with a diplomatic approach Swift understanding of new systems and processes. function in an evolving technical environment. A flexible attitude with respect to work assignments and new learning; ability to adjust rapidly to changing environments Customer focus to interact professionally and respectfully within Parexel and all external colleagues to build rapport and trust Commitment to first time quality, including a methodical and accurate approach to work activities Proficient presentation skills Time management and prioritization skills in order to meet objectives and timelines Proven problem-solving skills including capability to make appropriate decisions in ambiguous situations, ability to conduct root cause analyses Ownership and accountability relative to Key Accountabilities in Job Description Good business awareness/business development skills (including financial awareness). Ability to create, maintain and define strategies to improve the efficiency of running a clinical trial. Demonstrate commitment to refine quality processes