Bioclinica Released Job Openings On 21/06/2022.Bioclinica’s global team of life science experts serve more than 500 pharmaceutical, biotechnology, and device organizations – including the top 20 biopharmaceutical companies and leading CROs – through locations in North America, Europe, and Asia.
Vacancy Details:
Bioclinica Recruiting Bachelor s or Master s degree in computer science, life sciences or related field preferred with 01- 03+ Years of Experience for Clinical research Scientist Position.Complete Details for the Clinical research Scientist as follows.
Important Details :
- Location :Bangalore/Bengaluru
- No of Vacancies:01
- Details of Salary:NA
- Opening date for online Application:21/06/2022
- Mode of application :Online
- How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps
Related Job: Quality Control,Microbiology,Production,Packing Dept Walk In At Baxter
Job Description/Skills Required
Primary Responsibilities
Provides data to clients (internal and external) in functional format by:
- Creating and executing SAS edit check programs
- Validating edit check programs using standard validation practices and processes
- Creating, validating and executing SAS programs and macros
- Utilizing SAS programming skills to provide ad-hoc reports (external and internal)
- Assist in developing programming specifications
- Assist in creating program specific validation plans
- Identifying and implementing solutions for complex reporting needs
Ensures client data accuracy and integrity by:
- Creating and/or reviewing data editing and export specifications
- Working directly with clinical data manager, and where needed with clinical project manager and other team members to ensure specifications are clear and accurate.
- Has a clear understanding of the contextual requirements for reporting outputs; and provides feedback
- Programming data cleaning/consistency checking programs to support internal applications for all therapeutic areas
- Programming and testing data export programs in accordance with specific client needs
- Documenting all programming and validation efforts in accordance with Good Clinical Practices
- Monitoring data integrity throughout a given study
- Utilizing SDTM guidelines to create transfer datasets
- Participating in project meetings (internal and external)
Develops and maintains clinical programming standard operating procedures by:
- Participating in the development of data editing conventions, specification documents and Clinical Data Management (CDM) processes
- Contributing to, designing and maintaining a library of reusable code
- Leading and managing enhancements to current CDM systems and providing inputs in the implementation of new systems.
Ensures project timelines are maintained by:
- Working independently and efficiently with minimal input required from the manager. Reviewing timelines; and projecting estimates and target dates in conjunction with direct supervisor and project team
- Adhering to target dates for project timelines
- Communicating any changes in target date to appropriate personnel including Project Manager
- Keeping department head informed of progress as well as potential impediments
Maintains Quality Service and Departmental Standards by:
- Adhering to established processes and standards
- Reading, understanding and adhering to organizational Standard Operating Procedures (SOP)
- Assisting in establishing and enforcing departmental standards
- Maintain and review clinical programming SOPs
- Participating in the modification of company SOPs
Click here for Official notification and Apply
