Opening for Drug Safety Associate @ Synowledge Mysore, Karnataka
At Synowledge, our mission is to help our clients improve patients’ quality of life though cutting-edge technology solutions and innovative consulting services. With nearly 10 years’ experience, Synowledge has become a strategic partner with many Top 20 Pharma and Fortune 500 companies. Our technology solutions and innovative consulting services help life sciences companies reduce cost, accelerate growth and minimize time to market during the drug development lifecycle.
We are seeking to recruit a Drug Safety Associate to join our PV Services team with responsibility for case intake and case processing.
The successful candidate will have a Bachelor’s degree in Pharma/Life Sciences or a related discipline, have basic competence in medical, pharmaceutical and therapeutic terminology and familiarity with regulatory and pharmacovigilance guidelines.
The DSA will be responsible for processing and translating individual case safety reports from English to Japanese and vice versa, therefore fluency in both English and Japanese (written and spoken) is essential (University degree in Japanese or certified in JLPT N3 or higher)
Duties within this role will include
Responsible for Case intake, duplicate check , and registration
Responsible for Data entry of single cases into Safety Database Application
Review and evaluate AE case information to determine required action based on and following internal policies and procedures
Responsible for writing medically relevant Safety narrative of cases
Perform any other drug safety related activities as assigned
Perform Literature Review activities when trained and assigned
Skills required
Excellent Attention to Detail
Ability to work independently but guided by documented procedures
Very strong written and verbal communication skills
Relevant product and industry knowledge
Experience with relevant software applications
Creativity and the ability to think laterally
Excellent problem solver and multi-tasker
Strong computer literacy (MS Office)
Our success is founded on the dedication, passion and skills of our employees world-wide. If you are excited about this opportunity to work in a challenging and dynamic environment, please send your CV!
In addition to a competitive salary plus benefits, Synowledge offers the opportunity to work in a multinational environment with people passionate about what they do. We are committed to providing a great place to work and develop. We recognize that we spend a large part of our lives in work, so we want you to come to work each morning with a spring in your step, looking forward to the day ahead.
Click here to apply
At Synowledge, our mission is to help our clients improve patients’ quality of life though cutting-edge technology solutions and innovative consulting services. With nearly 10 years’ experience, Synowledge has become a strategic partner with many Top 20 Pharma and Fortune 500 companies. Our technology solutions and innovative consulting services help life sciences companies reduce cost, accelerate growth and minimize time to market during the drug development lifecycle.
We are seeking to recruit a Drug Safety Associate to join our PV Services team with responsibility for case intake and case processing.
The successful candidate will have a Bachelor’s degree in Pharma/Life Sciences or a related discipline, have basic competence in medical, pharmaceutical and therapeutic terminology and familiarity with regulatory and pharmacovigilance guidelines.
The DSA will be responsible for processing and translating individual case safety reports from English to Japanese and vice versa, therefore fluency in both English and Japanese (written and spoken) is essential (University degree in Japanese or certified in JLPT N3 or higher)
Duties within this role will include
Responsible for Case intake, duplicate check , and registration
Responsible for Data entry of single cases into Safety Database Application
Review and evaluate AE case information to determine required action based on and following internal policies and procedures
Responsible for writing medically relevant Safety narrative of cases
Perform any other drug safety related activities as assigned
Perform Literature Review activities when trained and assigned
Skills required
Excellent Attention to Detail
Ability to work independently but guided by documented procedures
Very strong written and verbal communication skills
Relevant product and industry knowledge
Experience with relevant software applications
Creativity and the ability to think laterally
Excellent problem solver and multi-tasker
Strong computer literacy (MS Office)
Our success is founded on the dedication, passion and skills of our employees world-wide. If you are excited about this opportunity to work in a challenging and dynamic environment, please send your CV!
In addition to a competitive salary plus benefits, Synowledge offers the opportunity to work in a multinational environment with people passionate about what they do. We are committed to providing a great place to work and develop. We recognize that we spend a large part of our lives in work, so we want you to come to work each morning with a spring in your step, looking forward to the day ahead.
Click here to apply
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