Sr Clinical Data Specialist Job Vacancy in Labcorp Bengaluru, Karnataka – Latest Jobs in Bengaluru, Karnataka

Are you looking for a New Job or Looking for better opportunities?
We got a New Job Opening for

Full Details :
Company Name : Labcorp
Location : Bengaluru, Karnataka
Position :

Job Description : Job Overview:Review clinical trial data in accordance with [Global] Data Management Plans and
applicable standardized data management processes (SOPs, Work Instructions, etc.) to
identify erroneous, missing, incomplete, or implausible data.
Run ancillary programs (e.g., diagnostics, special listings, reconciliation discrepancy
listings) used to support the review of clinical trial data.
Generate, resolve and track queries to address problematic data identified during data
review activities.
Perform aggregate review of clinical data by patient, site and / or project to identify
data trends (patient safety, compliance, etc.) and / or data inconsistencies that require
further investigation.
Apply quality control procedures and checks to ensure data quality standards (client
and Labcorp) are achieved.
Potentially serve as a reviewer of project documents such as protocols, CRFs (or eCRF
Completion guidelines, Data Management Plans, Perform Data review utilizing all
applicable documents such as protocols, CRFs (or eCRFs and eDiary) etc.
Assist with the development of [Global] Data Management Plans and Quality
Management (QM) Plans that will deliver accurate, timely, consistent, and quality
clinical data.
Assist in the review of the database design and annotate the CRF (eCRF) according to
the specifications.
Create and assist in the data review guidelines, make sure to be consistent with the
clinical data model, and CRF/eCRF completion / monitoring conventions.
Assist in the development and testing of data management system edit / data validation
checks (diagnostics) and special listings / procedures used as tools for the data review
and discrepancy management activities.
May assist with the Lead Data Manager or Lead Data Reviewer to build timelines to
meet contracted milestones by communicating with leads in different disciplines and
the full project team as necessary.
Knowledge of Data Management tools, systems, and processes.Ensures service and quality, meet agreed upon specifications per the DMP and scope of
work in the budget.
Inform Lead Data Reviewer of overages in budgeted units and assist in Change Order
Log process, if applicable.Perform quality control on data management activities as appropriate to include, but
not be limited to all study documentation, query generation and integration; to ensure
that internal and client quality standards are achieved.
Support and action client or internal audits as appropriate and resolve all issues within
an appropriate timeframe. Address client comments with the study team, as
appropriate.
Mentor / Coach in training of project staff on project-specific, global, standardized data
management processes.
Performs other related duties as assigned by management.
Education/Qualifications:University / college degree (life sciences, health sciences, information technology or
related subjects preferred).
Experience and/or education plus relevant work experience, equating to a bachelor’s degree
will be accepted in lieu of a bachelor’s degree.
Experience:4 to 6 years of Clinical Data Management.Some knowledge of clinical trial process, DM, clinical operations, biometrics, and system
applications to support operations.
Time management skill and ability to adhere to project productivity metrics and timelines.Ability to work in a team environment and collaborate with peers.Good organizational ability, communication, and interpersonal skills.Team working skills and good collaborator skills.Knowledge of medical terminology is preferred.Knowledge of science or a scientific background is preferred.Good oral and written communication skills.

This post is listed Under Healthcare

Disclaimer : Hugeshout works to publish latest job info only and is no where responsible for any errors. Users must Research on their own before joining any company