Senior Data Acquisition Specialist Parexel

5.0 - 9.0 years

0 Lacs

maharashtra

On-site

You will be working as a Data Acquisition Specialist with a minimum of 5 years of experience in the Data Acquisition domain. Your role will involve being an expert in handling Non-CRF activities and working independently on the non-CRF data strategy. You should have a deep understanding of Data Management conventions, data standards, processes, and drug development processes. Additionally, you will be expected to have experience with Study conventions, including non-CRF collection data standards, processes, knowledge sharing, and best practices on assigned studies. Your responsibility will also include influencing the Study Team to adhere to non-CRF guidance, processes, and negotiating conti...

Posted 4 months ago

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Clinical Data Engineer II Parexel

5.0 - 9.0 years

0 Lacs

maharashtra

On-site

You are a Data Acquisition Specialist with a minimum of 5 years of experience in the Data Acquisition domain. You possess expertise in handling Non-CRF activities and are capable of working independently on the non-CRF data strategy. Your role requires an in-depth understanding of Data Management conventions, data standards, Processes, and Drug development Process. You have experience with Study conventions, including non-CRF collection data standards, Processes, Knowledge sharing, and best practices on assigned studies. Your responsibility involves influencing the Study Team to adhere to non-CRF guidance, processes, and negotiating contingency plans to mitigate delays in deliverables. Your ...

Posted 4 months ago

AI Match Score

Apply

Clinical Data Engineer Parexel

5.0 - 9.0 years

0 Lacs

maharashtra

On-site

You are a Data Acquisition Specialist with a minimum of 5 years of experience in the Data Acquisition domain. You possess expertise in handling Non-CRF activities and can work independently on the non-CRF data strategy. Your role requires an in-depth understanding of Data Management conventions, data standards, processes, and Drug development processes. Additionally, you have experience with Study conventions, including non-CRF collection data standards, processes, knowledge sharing, and best practices on assigned studies. Your responsibility includes influencing the Study Team to adhere to non-CRF guidance, processes, and negotiating contingency plans to mitigate delays in deliverables. You...

Posted 4 months ago

AI Match Score

Apply

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