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Recruit for the post of Associate, Associate Data Manager

2.00 to 4.00 Years   Chennai   27 Oct, 2022
PFIZER LIMITED
Job LocationChennai
EducationNot Mentioned
SalaryNot Disclosed
IndustryPharma / Biotech
Functional AreaFinance / Accounts / Tax
EmploymentTypeFull-time

Job Description

    Why Patients Need YouAs part of the Data Monitoring and Management group, an integral delivery unit within the Global Biometrics and Data Management (GBDM) organization, the Associate Data Manager is responsible for timely and high quality data review and query management of clinical data supporting the Pfizer portfolio. The Associate Data Manager executes on key data management deliverables used to collect, review, monitor, and ensure the integrity of clinical data.What You Will AchieveIt is our mission to strengthen the oversight of our clinical data through stronger ownership, control, and visibility. You will play an important role in processing, reviewing and receiving clinical data and records and from therapeutic groups as well as internal and outside investigators. You will ensure that accurate, timely, and consistent data reaches the clinical teams and other groups. You will be relied on for data management plans including data preparation and validation activities, among others.As an associate, your focus on the job will contribute in achieving project tasks and goals. Through your domain knowledge and commitment, you will create a collaborative team environment for your colleagues.It is your commitment and hard work that will help make Pfizer ready to achieve new milestones and help patients across the globe.ROLE RESPONSIBILITIES
    • Participate in DMM activities including data review and query management, assist with quality database design including documentation, testing, validation, and implementation of clinical data collection tools, CRF and non-CRF, using an electronic data capture (EDC) system and/or other data collection systems.
    • Ensure work carried out in accordance with applicable SOPs and working practices.
    • Assist with the required study-specific DMM documents in the Trial Master File (TMF) are of high quality and are filed contemporaneously to support downstream inspection and submission readiness activities.
    • Assist with operational excellence in collaboration with Data Manager and CDS for application of standards, data acquisition, proactive data review and query management, data cleaning, e-data processing, data access and visualization, DM metrics reporting, database release, and submission related activities
    • Support complex data review activities, without support, on one or more studies/Assets
    QUALIFICATIONS
    • Awareness of clinical development and pharmaceuticals as a regulated industry
    • Awareness of healthcare regulatory authorities (e.g. FDA, Health Canada)
    • Ability to learn clinical data management processes and principles in area of responsibility.
    • Demonstrates required verbal and written communication skills including ability to communicate remotely
    • Capable to learn technical data systems
    • Capable to learn how to use data visualization tools (e.g. Spotfire, J-Review)
    • Awareness of MedDRA/WHO-Drug preferred
    • Proficiency in the use of Microsoft Office Suite of tools (Outlook, Word, Excel, etc.)
    • Bachelor s degree minimum requirement. Health Sciences experience or Technology degree preferred.
    • At least 2 year experience in Clinical Data Management, performing data review activities, in a CRO or a Pharma Company.
    Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.Medical #LI-PFE,

Keyskills :
data managementprogrammingdata collectionresearchdata entry

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