Opening for experienced Drug Safety Physician @ Accenture
Job Description
Schedule : Full-time
Conduct a full medical assessment of all serious and Non-Serious Cases;
Upgrade a Non-Serious Case to a Serious Case, where applicable, following the medical assessment;
Review and modify the data entered in respect of a Case as necessary and in accordance with applicable SOPs; and
Approve Serious and Non-Serious Cases.
Accenture shall assume the following responsibilities and perform the following activities with regard to Signal Detection:
Participate in Signal Detection meetings, as requested by Client; and
Provide client with line listings and summary tabulations for each Signal Detection Request.
Salary: Not Disclosed by Recruiter
Industry: IT-Software / Software Services
Functional Area: Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology
Role Category: Drug Regulatory Director
Role: Drug Regulatory Director
Keyskills: mbbs,clinical research,clinical data management,medical affairs,drug safety,fda,ms office,pv,emea,asr
Desired Profile
MD/MBBS (board certified) as a minimum, a higher medical speciality is preferred; A minimum of 2 - 4 years experience in a clinical practice; A minimum of 1.5 - 3 years experience in pharmaceutical industry (PV, clinical Research, Medical Affairs areas of experience are preferred); Thorough knowledge of Word and Excel required; Experience in reviewing data listings and safety reports from clinical trials; Sound medical knowledge; Well organized, structured person, with a logic approach to issues raised; Ability to comprehend and interpret clinical data; Understanding of complexities of pharmacovigilance is preferred; Commitment to quality and constantly seeking to improve it; Understanding of pharmacovigilance regulations is preferred; Excellent English oral and written skills are a must. Ability to write and edit safety report;
Education:UG -MBBS - Medicine
PG - M.S/M.D - Any Specialization
Doctorate - Any Doctorate - Any Specialization, Doctorate Not Required
Company Profile
About Accenture Accenture is a global management consulting, technology services and outsourcing company, with more than 323,000 people serving clients in more than 120 countries. Combining unparalleled experience, comprehensive capabilities across all industries and business functions, and extensive research on the worlds most successful companies, Accenture collaborates with clients to help them become high-performance businesses and governments. The company generated net revenues of US$30.0 billion for the fiscal year ended Aug. 31, 2014. Its home page is www.accenture.com.
Click here to apply
Job Description
Schedule : Full-time
Conduct a full medical assessment of all serious and Non-Serious Cases;
Upgrade a Non-Serious Case to a Serious Case, where applicable, following the medical assessment;
Review and modify the data entered in respect of a Case as necessary and in accordance with applicable SOPs; and
Approve Serious and Non-Serious Cases.
Accenture shall assume the following responsibilities and perform the following activities with regard to Signal Detection:
Participate in Signal Detection meetings, as requested by Client; and
Provide client with line listings and summary tabulations for each Signal Detection Request.
Salary: Not Disclosed by Recruiter
Industry: IT-Software / Software Services
Functional Area: Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology
Role Category: Drug Regulatory Director
Role: Drug Regulatory Director
Keyskills: mbbs,clinical research,clinical data management,medical affairs,drug safety,fda,ms office,pv,emea,asr
Desired Profile
MD/MBBS (board certified) as a minimum, a higher medical speciality is preferred; A minimum of 2 - 4 years experience in a clinical practice; A minimum of 1.5 - 3 years experience in pharmaceutical industry (PV, clinical Research, Medical Affairs areas of experience are preferred); Thorough knowledge of Word and Excel required; Experience in reviewing data listings and safety reports from clinical trials; Sound medical knowledge; Well organized, structured person, with a logic approach to issues raised; Ability to comprehend and interpret clinical data; Understanding of complexities of pharmacovigilance is preferred; Commitment to quality and constantly seeking to improve it; Understanding of pharmacovigilance regulations is preferred; Excellent English oral and written skills are a must. Ability to write and edit safety report;
Education:UG -MBBS - Medicine
PG - M.S/M.D - Any Specialization
Doctorate - Any Doctorate - Any Specialization, Doctorate Not Required
Company Profile
About Accenture Accenture is a global management consulting, technology services and outsourcing company, with more than 323,000 people serving clients in more than 120 countries. Combining unparalleled experience, comprehensive capabilities across all industries and business functions, and extensive research on the worlds most successful companies, Accenture collaborates with clients to help them become high-performance businesses and governments. The company generated net revenues of US$30.0 billion for the fiscal year ended Aug. 31, 2014. Its home page is www.accenture.com.
Click here to apply
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