Average salary: Rs667,856 /yearly
More statsSearch Results: 68 vacancies
...quality of the relevant sections of the Trial Master File (local and central). May participate in the design and development of CRFs, CRF guidelines, patient informed consent templates and other protocol specific documents as the need arises. Collaborates with the project...
...medium complexity studies
Conduct overall statistical review of TFLs for medium complexity studies prior to client delivery
Review CRF and other study specific specifications and plans May perform sample size calculation for Clinical Pharmacology studies under the...
...Organizational skills with ability and willingness to work under pressure and manage time and priorities effectively
. Support for MI to prepare CRF (Client Return Forums)
. Tiering & Loan-To-Book data & report management (e.g. keeping a golden source, UCRM update uploads, regular...
Rs 6 lakh p.a.
...production of assigned mailing creation that is accurate and efficiently configured for deployment per the client's Campaign Request Form (CRF) instructions including the following:
■ Manages building and testing of campaign builds, including creative rendering, link...
...experience in pharmaceutical industry and preferably 2 plus years within clinical data management systems.
Understanding of protocol, CRF standards, Inform Terminologies and EDC data structure.
~ Knowledge and experience in Programming languages & experience in python or...
...tools
Strong CATIA , DMA ENOVIA skill to perform design activity.
Desirable:
Rolling stock structure design
Knowledgeable of CRF manufacturing
Meshing tool & basic hand calculation
Competencies & Skills
Structural Design
Sheet Metal Design
CATIA V5...
...within clinical data management systems.
Working knowledge of programming languages: Python, R & R Shiny.
Understanding of protocol, CRF standards, and EDC data structure
Experience in creating reports and visualizations using BI applications such as Tableau and Power...
...chart, electronic CRFs (eCRF), External Specifications, and SDTM Domains.
Prepare & review metadata specification (as relevant) and CRF. Submit requests to Standards Teams to either deviate from an existing standard or use a trial-specific element in alignment with the Lead...
...study including assisting in preparing the eCRF, CCGs, DMPs,
DVPs and performing User Acceptance Testing (UAT) if required.
Review CRF / eCRF data for completeness, accuracy, and consistency via computerized edits and
manual data checks.
Generate and close/...
...clinical data management systems.
~ Working knowledge of programming languages: Python, R R Shiny.
~ Understanding of protocol, CRF standards, and EDC data structure
~ Experience in creating reports and visualizations using BI applications such as Tableau and...
...work across protocols.
• Study Start up: Assist with protocol development, sample size calculation, protocol and case report form (CRF) review.
• Protocol: Authors or performs quality control (QC) review of the statistical section of a protocol (making best possible...
...Implementationand adherence to Project standards template in EDC and DMW.
Align with the PDMs to understand the project requirements (CRF and external data) for new programs/projects.
Ensure the design and set-up of study databases for clinical trials are aligned across...
...such as training and serving as primary contact for clinical questions
Activities related to data generation and validation, including CRF design, clinical data review/query resolution; ensure consistent, quality data review by supporting CS team
Clinical data trend...
...product, study supplies, special equipment, safety lab kits, etc.).
In collaboration with the data management group, ensures that the CRF complies with the protocol and Sponsor requirements and ensures queries resolution and data review process follow the study timelines...
...Senior Statistical Programmer is accountable for:
Provide programming input to the setup of the trial, including but not limited to the CRF, Trial Validation Plan and Data Flow Plan.
Responsible for creating and gathering input to the Specification ADRG for the clinical...
...Real world Clinical Research and Publications - Planning and Execution (including development of relevant documents viz. protocol, CRF, CSR, manuscript etc)
Advisory board meetings
Developing Insight driven Medical Plans
Interaction & Engagement of identified Key...
...with a programming background and preferably 5-plus years within clinical data management systems.
~ Good Understanding of protocol, CRF standards, and EDC data structure.
~ Proficient in working with programming languages: Python, R R Shiny.
~ Knowledge of ETL...
...pharmaceutical industry with programming background and preferably 2 years within clinical data management systems
~ Understanding of protocol, CRF standards, Inform Terminologies and EDC data structure
~ Knowledge and experience in Programming languages such as Python, R &...
...analyses.
Ensure that documents, specifications, programs/macros are consistent and comply with company standards by providing input into CRF and data structures tables, listings and figures for Interventional and Non-Interventional Clinical studies.
Maintain efficient...
...Responsible for implementation and maintenance of standard template in EDC and DMW. Align with the PDMs to understand the project requirements (CRF and external data) for new programs/projects.
• Responsible for tracking and implementation of the new requests for DMW template...
