Bioclinica Recruitment 2021.Bioclinica Notification full detailes below.Bioclinica is specifically structured to create clarity in the clinical trial process—so you can make better decisions. Bioclinica is divided into three business segments to deliver focused service supporting multifaceted technologies.
Important Vacancy details:
- Post Name: Jr. Drug Safety Associate
- Location:Mysore, India
- Salary: NA
- Openings:NA
Job Description: Hiring For Jr. Drug Safety Associate in Bioclinica !
Essential Duties and Responsibilities:
As Case Intake Member:
- Responsible for case intake, duplicate check, and registration
- Maintain log of source documents and other communications
As Case Processor:
- Responsible for data entry of individual case safety reports into the safety database.
- Review and evaluate AE case information to determine required action based on and following internal policies and procedures
- Process all incoming cases in order to meet timelines
- Full data entry including medical coding and safety narrative
As Medical Coder
Responsible for coding all medical history, events, drugs /procedures/indications and laboratory tests according to the appropriate dictionary (For e.g. MedDRA, Company Product Dictionary, WHO-DD)
As Narrative Writer
Responsible for writing medically relevant safety narrative of cases and checking the completeness and accuracy of the data entered in the various fields.
As Literature Review Specialist
- Ensure effective and accurate collection, recording, review and reporting of literature searches conducted.
- Review of literature articles to identify case safety reports.
- Responsible for operational Pharmacovigilance activities for assigned developmental and/or marketed products.
- Assist in signal generation and safety analysis activities.
- Ensure quality of literature searches and reporting.
- Review of local/global literature reports to determine regional reportability.
- Create/maintain study summary documents.
- Assist with narrative writing for periodic/ad hoc submissions.
- Assist with ad hoc or routine safety monitoring activities.
Other Responsibilities:
- Following up with sites regarding outstanding queries.
- Follow up on reconciliation of discrepancies.
- Follow departmental AE workflow procedures
- Closure and deletion of cases
- Perform any other drug safety related activities as assigned
Specialized knowledge and skills:
- Basic competence with medical and therapeutic terminology.
- Ability to work independently but guided by documented procedures, with appropriate support.
- Able to work effectively as part of a team.
- Understanding of patient safety regulatory obligations.
- Should be familiar regulatory &pharmacovigilance guidelines.
- Should be familiar with pharmacovigilance terminology.
- Excellent attention to detail.
- Ability to deliver within established timelines.
- Fluency in English and excellent comprehension.
- Computer literate.
Communication Skills:
Requires a proactive approach and excellent written/oral communication and interpersonal skills. Strong interpersonal skills required to interact with clients, management, and peers effectively. Effective cross- department communication. Ability to document and communicate problem/resolution and information/action plans.
Selection Process: The selection will be on the basis of Interview.
How to Apply : Click here for full details and Apply Online