Upload Button Icon Add office photos
filter salaries All Filters

30 Syneos Health Jobs

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 11d ago

Job Description

Description
Safety & Pharmacovigilance Specialist I
Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.
Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.
Discover what our 29,000 employees, across 110 countries already know:
WORK HERE MATTERS EVERYWHERE
Why Syneos Health
  • 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%)
Get to know Syneos Health
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
No matter what your role is, you ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health .
Additional Information:
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

Employment Type: Full Time, Permanent

Read full job description

Prepare for Japanese Language Expert roles with real interview advice

What people at Syneos Health are saying

Japanese Language Expert salary at Syneos Health

reported by 5 employees with 1-3 years exp.
₹7.2 L/yr - ₹9 L/yr
13% more than the average Japanese Language Expert Salary in India
View more details

What Syneos Health employees are saying about work life

based on 571 employees
82%
95%
89%
96%
Flexible timing
Monday to Friday
No travel
Day Shift
View more insights

Syneos Health Benefits

Submitted by Company
Financial Health
Learning, Development and Growth
Physical Health
Employee Resources
Submitted by Employees
Work From Home
Health Insurance
Job Training
Soft Skill Training
Cafeteria
Team Outings +6 more
View more benefits

Compare Syneos Health with

IQVIA

3.9
Compare

Parexel International

3.9
Compare

ICON Plc

4.2
Compare

Fortrea Development India Private Limited

3.9
Compare

WuXi AppTec

3.1
Compare

Syngene International

3.9
Compare

Aragen Life Sciences

4.0
Compare

SAI Life Sciences

3.9
Compare

Lambda Therapeutic Research

4.5
Compare

Reliance Life Sciences

3.5
Compare

Aizant Drug Research Solutions

3.9
Compare

Veeda Clinical Research

3.9
Compare

Equinox Labs

3.8
Compare

Rubicon Research

3.4
Compare

Cliantha Research

4.0
Compare

Accutest Research Laboratories

3.6
Compare

Navitas Life Sciences

3.5
Compare

Raptim Research

4.0
Compare

Axis Clinicals

4.0
Compare

Spc Life Sciences

3.5
Compare

Similar Jobs for you

Chinese Language Expert at Syneos Health

Kolkata, Mumbai + 5

2-6 Yrs

₹ 4-8 LPA

Senior Drug Safety Associate at Eversana India

Pune

3-7 Yrs

₹ 5-9 LPA

Research Lead at Sanofi India Ltd

Hyderabad / Secunderabad

2-5 Yrs

₹ 9-13 LPA

Safety Expert at Sandoz

Warangal, Hyderabad / Secunderabad + 1

3-7 Yrs

₹ 8-12 LPA

Medical Data Reviewer at IQVIA

Bangalore / Bengaluru

2-6 Yrs

₹ 3-6 LPA

Safety Specialist at Azurity Pharmaceuticals

Hyderabad / Secunderabad

2-6 Yrs

₹ 4-8 LPA

Biostatistician at Syneos Health

Kolkata, Mumbai + 5

4-8 Yrs

₹ 6-10 LPA

Biostatistician at Syneos Health

Kolkata, Mumbai + 5

5-10 Yrs

₹ 7-12 LPA

Medical Reviewer at MMS Holdings Inc.

Bangalore / Bengaluru

4-9 Yrs

₹ 6-10 LPA

Biostatistician at Syneos Health

Kolkata, Mumbai + 5

4-7 Yrs

₹ 6-9 LPA

Japanese Language Expert - Safety & PV Specialist

4-7 Yrs

Kolkata, Mumbai, New Delhi +4 more

11d ago·via naukri.com

Principal Stat Programmer (ADAM, TLFs , SDTM)

11-12 Yrs

Kolkata, Mumbai, New Delhi +4 more

11d ago·via naukri.com

Principal Stat Programmer

10-12 Yrs

Kolkata, Mumbai, New Delhi +4 more

11d ago·via naukri.com

Principal Stat Programmer (ADAM, TLFs , SDTM)

11-12 Yrs

Kolkata, Mumbai, New Delhi +4 more

11d ago·via naukri.com

Sr Medical Writer - (Process Mapping , Scientific Writer)

1-4 Yrs

Kolkata, Mumbai, New Delhi +4 more

11d ago·via naukri.com

Manager Biostatistics

2-3 Yrs

Kolkata, Mumbai, New Delhi +4 more

11d ago·via naukri.com

Stat Programmer II / Sr Stat Programmer / Prin Stat Programmer

2-6 Yrs

Kolkata, Mumbai, New Delhi +4 more

11d ago·via naukri.com

Sr Medical Writer - (CSR, ICF) Regulatory

2-5 Yrs

Kolkata, Mumbai, New Delhi +4 more

11d ago·via naukri.com

Chinese Language Expert - Safety & PV Specialist I

2-6 Yrs

Kolkata, Mumbai, New Delhi +4 more

11d ago·via naukri.com

Clinical Programmer II (DM SAS)

2-7 Yrs

Kolkata, Mumbai, New Delhi +4 more

11d ago·via naukri.com
write
Share an Interview