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Medical Reviewer with English
Accenture Services, s.r.o.
Place of work
Prague, The Capital Prague
Prague, The Capital Prague
Contract type
full-time
full-time
Information about the position
Job description, responsibilities and duties
Join an interesting project supporting an international pharmaceutical company
by performing timely data processing in the safety database for received source
documents of cases collected during safety monitoring of drugs and compounds.
In this position you would be responsible for medical review and assessment of
Adverse Events within agreed timeframes and to a high standard of accuracy, in
compliance with Customer business rules, standard operating procedures and
global regulatory requirements as documented in Customer’s SOPs.
Additionally, the Medical Reviewer ensures integrity and consistency of data
against source document by performing QC and appropriate correction of all
processed cases in appropriate timelines as per standard operation procedures.
What are your responsibilities?
* Review and verify appropriate selection of adverse events from source
documents, assign appropriate MedDRA code, assess labeling, review narrative and
provide company comment in accordance with client requirements
* Acquire and maintain current knowledge of product portfolio and safety
profiles of for products across therapeutic areas
* Identify, escalate and resolve case issues, co-ordinate with client
therapeutic team/site for specific products or functional groups
* Communicate and interact effectively
* Follow up with sites regarding outstanding queries
* Follow up on reconciliation of discrepancies
* Perform other drug safety related activities as assigned
ARE YOU OUR IDEAL CANDIDATE?
* Medical Degree from EU university required (e.g. MUDr., MBBS, M.D.)
* Minimum 1 year of clinical experience
* Fluency in English
* Very good competency with medical and therapeutic terminologies
* Ability to read and understand medical source documents and to summarize them
in a well-written narrative
* Familiar with regulatory & Pharmacovigilance guidelines & Pharmacovigilance
terminology
* High level of accuracy and attention to detail
* Experience and skills in working on computers (word processing, spreadsheets,
safety database tools)
* Proficiency in prioritizing assignments and ability to adapt to rapidly
changing priorities
* Good knowledge of business regulations and standards an advantage
* Good written, verbal and organizational skills
by performing timely data processing in the safety database for received source
documents of cases collected during safety monitoring of drugs and compounds.
In this position you would be responsible for medical review and assessment of
Adverse Events within agreed timeframes and to a high standard of accuracy, in
compliance with Customer business rules, standard operating procedures and
global regulatory requirements as documented in Customer’s SOPs.
Additionally, the Medical Reviewer ensures integrity and consistency of data
against source document by performing QC and appropriate correction of all
processed cases in appropriate timelines as per standard operation procedures.
What are your responsibilities?
* Review and verify appropriate selection of adverse events from source
documents, assign appropriate MedDRA code, assess labeling, review narrative and
provide company comment in accordance with client requirements
* Acquire and maintain current knowledge of product portfolio and safety
profiles of for products across therapeutic areas
* Identify, escalate and resolve case issues, co-ordinate with client
therapeutic team/site for specific products or functional groups
* Communicate and interact effectively
* Follow up with sites regarding outstanding queries
* Follow up on reconciliation of discrepancies
* Perform other drug safety related activities as assigned
ARE YOU OUR IDEAL CANDIDATE?
* Medical Degree from EU university required (e.g. MUDr., MBBS, M.D.)
* Minimum 1 year of clinical experience
* Fluency in English
* Very good competency with medical and therapeutic terminologies
* Ability to read and understand medical source documents and to summarize them
in a well-written narrative
* Familiar with regulatory & Pharmacovigilance guidelines & Pharmacovigilance
terminology
* High level of accuracy and attention to detail
* Experience and skills in working on computers (word processing, spreadsheets,
safety database tools)
* Proficiency in prioritizing assignments and ability to adapt to rapidly
changing priorities
* Good knowledge of business regulations and standards an advantage
* Good written, verbal and organizational skills
Requirements for the employee
Candidates with education suit the position
Secondary with school-leaving examination
Language skills
English - Upper intermediate (B2)
Advertiser
Brief description of the company
Accenture’s Services workforce is a dedicated team of people who work on outsourcing engagements. These are long-term partnerships with clients for whom we manage and provide increasingly specialized business operations, such as finance and accounting, IT, applications development and maintenance, help desk services, and HR. We not only maintain key business functions for clients, we constantly seek to improve them to help our clients move ahead of the competition.
Number of employees
1000 and more employees
ID: 3290937
Datum zveřejnění: 20.1.2018
2018-01-20
lokalita: The Capital Prague Pozice: Administrative Worker, Official Společnost: Accenture Services, s.r.o.
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