7 Clinical Data Jobs in Ahmedabad
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ICSR Pharmazone - Ahmedabad, IN Proficiency in Clinical trial cases and Data entry processes Knowledge of Drug safety guidelines and regulations Strong attention to detail and accuracy in ICSR activities Ability to work effectively in a team 300000 - 500000 per year More than 30 days ago
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Clinical Research Associate Pharmazone - Ahmedabad, IN Hello Jobseekers!! Greetings From Pharmazone!! We are hiring!! Position- Clinical Research Associate Location- Ahmedabad Qualification - Master Degree Pharma/ Science Job Description: On-Site Review More than 30 days ago
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Group Functional Lead Cell Based Bioassays Lambda Therapeutic Research - Ahmedabad(Gota) of regulatory submissions to support IND enabling data to initiate early development clinical trials. Identify and communicate best practices within the CDMO function. Develop and maintain a highly capable Not disclosed INR 8 days ago
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Senior Regulatory Affairs Officer Aegis Lifesciences Pvt Ltd - Ahmedabad, India experience operating in a regulated environment Ability to read, analyze and interpret governmental regulations & reports, scientific or clinical publications and data Ability to write reports, business Not Mentioned 14 days ago
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Clinical Research Associate Pharmazone - Ahmedabad, India ) Experience with Bioanalytical processes Familiarity with Clinical Research Associates (CRA) responsibilities Understanding of Clinical Research Organizations (CRO) Proficient in monitoring clinical trials Not Mentioned 13 days ago
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Clinical Research Associate Pharmazone - Ahmedabad, India Hello Jobseekers!! Greetings From Pharmazone!! We are hiring!! Position- Clinical Research Associate Location- Ahmedabad Qualification - Master Degree Pharma/ Science Job Description On-Site Review Not Mentioned More than 30 days ago
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Specialist, PV Baxter Medical Devices - Ahmedabad, India outsource vendor through random QC of cases or through review of aggregate data - Provide training to outsource vendor - Process spontaneous, solicited, clinical and literature adverse event reports as a part Not Mentioned More than 30 days ago
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