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Japanese Language Expert - Safety & PV Specialist
4-7 years
Kolkata, Mumbai, New Delhi + 4 more
1 vacancy
Japanese Language Expert - Safety & PV Specialist
Syneos Health
posted 16d ago
Job Role Insights
Flexible timing
Key skills for the job
Job Description
- We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
- We are committed to our Total Self culture - where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
- We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives - we re able to create a place where everyone feels like they belong.
Job responsibilities
- Coordinates workflow to ensure delivery of project.
- May be responsible for distributing and monitoring team workload.
- Escalates issues with project deliverables, finance and quality to Safety Program Delivery Lead/Manager or Line Manager as appropriate in a timely manner.
- Provides support to manage safety and pharmacovigilance project risks/ issues as required.
- Understands financial measures, work orders, performance metrics (including quality parameters, monthly budget reports, and changes in scope) and project budgets.
- Assists in the preparation of project plans such as Safety Management Plan.
- Assists in the preparation and participates in internal project review meetings as required.
- May perform set-up, delivery, and close-out of safety and pharmacovigilance projects.
- Maintains safety tracking for assigned activities.
- May enter information into SPVG quality and tracking systems for receipt and tracking ICSR.
- May process ICSRs according to Standard Operating Procedures (SOPs) and project/program- specific safety plans.
- Triages ICSRs, evaluates ICSR data for completeness, accuracy, and regulatory report ability.
- Enters data into safety database.
- Codes events, medical history, concomitant medications, and tests.
- Compiles complete narrative summaries.
- Assesses information to be queried and follows up until information is obtained and queries are satisfactorily resolved.
- Participates in the generation of timely, consistent, and accurate reporting of expedited reports in accordance with applicable regulatory requirements.
- Coordinates with data management staff concerning reconciliation of safety data between the clinical and safety databases.
- May perform or participate in quality control of literature screening and review for safety, drug coding, maintenance of drug dictionary, MedDRA coding.
- Validation and Submission of xEVMPD product records, including appropriate coding of indication terms using MedDRA.
- Manual recoding of un-recoded product and substance terms arises from ICSRs.
- Identification and management of duplicate ICSRs.
- Activities related to SPOR / IDMP.
- Quality review of ICSRs.
- Quality review for the work performed by peers.
- Serves as a subject matter expert in SPVG, which includes resolution of project related routine queries, mentoring, and coaching.
- Managing a small team within the project.
- Ensures distribution of all required individual expedited and periodic reports for both clinical and post-marketing projects to the Safety Submissions team if contracted to submit the reports.
- Provides training of Investigators on ICSR reporting or training to project team members for appropriate project related activities.
- Participate in audits/inspections as required.
- Ensures all relevant documents are submitted to the Trial Master File (TMF) as per company SOP/Sponsor requirements for clinical trials and the Pharmacovigilance System Master File for post-marketing programs as appropriate.
- Maintains understanding and compliance with SOPs, Work Instructions (WIs), global drug/biologic/device regulations, GCP, ICH guidelines, GVP, project/program plans and the drug development process.
- Applies safety reporting regulatory intelligence maintained by Syneos Health to all safety reporting activities.
Qualifications
What we re looking for
- Bachelor s Degree in life science, registered nurse, pharmacist or an equivalent combination of education and experience that gives the individual the necessary knowledge, skills and abilities to perform the job.
- Safety Database systems and knowledge of medical terminology required
- In depth understanding of clinical trial process across Phases II-IV and/or post-marketing safety requirements, ICH GCP, GVP and regulations related to Safety and Pharmacovigilance
- Proficiency in Microsoft Office Suite (Word, Excel and PowerPoint), Visio, email (Outlook), TeamShare (or other management/shared content/workspace) and internet.
- Ability to work independently and in a team environment
- Strong communication, presentation, interpersonal skills, both written and spoken
- Strong organizational skills with proven ability to prioritize and work on multiple tasks and projects
- Detail oriented with a high degree of accuracy and ability to meet deadlines
- Able to make effective decisions
- Minimal travel may be required (up to 10%)
Employment Type: Full Time, Permanent
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What people at Syneos Health are saying
Japanese Language Expert salary at Syneos Health
reported by
4
employees
with 1-2
years exp.
₹7.2
L/yr - ₹9
L/yr
18%
more
than the average Japanese Language Expert Salary in India
View more details
What Syneos Health employees are saying about work life
based on 559 employees
Flexible timing
Monday to Friday
No travel
Day Shift
Syneos Health Benefits
Submitted by Company
Financial Health Learning, Development and Growth Physical Health Employee Resources
Submitted by Employees
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