Job Description Provide timely and professional ongoing management of clinical trial data by identifying and resolving errors and inconsistencies in eCRF data to ensure consistently high standard database(s) with respect to cost, quality and timelines.Key Areas1.Provide professional DM input on Clinical Trial Team(s)2.Input to and review of clinical trial database design including User Acceptance Test-ing (UAT).3.Responsible for the Validation and Analysis Plan (VAP) meeting for the clinical trial, which includes chairing the meeting, writing the study specific validation checks and necessary reports to ensure high quality and consistent data.4.Identify errors and inconsistencies; resolve them or initiate their resolution either via the field monitor or directly with the investigational site, to ensure high quality and timely database locks.5.Review and contribute to preparation of protocols, specifically related to the data management section, visit schema and study design.6.Prepare Case Report Forms (CRFs) and CRF completion Guidelines (CCGs), elec-tronic or paper.7.Support and provide leadership for data management staff for allocated trials.8.Freeze and lock data as appropriate in time for statistical review, blinded interim quality review, interim and final database lock.9.Perform training on data management software and practices or trial specific topics as required.10.Prepare training materials for data management activities and processes as re-quired.11.Travel is required as needed.
Desired Profile :1. 2 or more years experience in drug development with at least 2-10 years experience in Data Management.2.University Science Degree in life sciences, pharmacy, nursing or equivalent relevant experience.3.Excellent written and oral English skills 4.Understanding of clinical trial methodology, GCP and medical terminology5.Good computer skills6.Good organizational and project management skills.7.Good communication and interpersonal skills8.Intermediate presentation and problem solving skills9.Ability to work well in a team 10.May coordinate and provide direction on task to other data management team members
Experience 3 - 8 Years
Education UG - Any Graduate - Any Specialization PG - Any PG Course - Any Specialization
Location Hyderabad / Secunderabad
Contact Meghna Novartis Healthcare Pvt Ltd iLabs Centre, No. 18, Software Units Layout Madhapur Hyderabad - Andhra Pradesh ,INDIA 500081
Telephone0 40-66576598
Website http://www.novartis.com
Desired Profile :1. 2 or more years experience in drug development with at least 2-10 years experience in Data Management.2.University Science Degree in life sciences, pharmacy, nursing or equivalent relevant experience.3.Excellent written and oral English skills 4.Understanding of clinical trial methodology, GCP and medical terminology5.Good computer skills6.Good organizational and project management skills.7.Good communication and interpersonal skills8.Intermediate presentation and problem solving skills9.Ability to work well in a team 10.May coordinate and provide direction on task to other data management team members
Experience 3 - 8 Years
Education UG - Any Graduate - Any Specialization PG - Any PG Course - Any Specialization
Location Hyderabad / Secunderabad
Contact Meghna Novartis Healthcare Pvt Ltd iLabs Centre, No. 18, Software Units Layout Madhapur Hyderabad - Andhra Pradesh ,INDIA 500081
Telephone0 40-66576598
Website http://www.novartis.com
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