Technical Analyst (23434) - Alpha Professional Resources, A.P.R., Inc. (AlphaProTemps) (thousand
Company Description:
Job Description:
Technical Analyst :
23434 Bachelor's Degree in life science, computer science, engineering, business or related discipline - 4 or more years of experience in clinical operations, clinical development or clinical quality assurance - Experience implementing clinical systems, such as CTMS, EDC, IVRS, ePRO or other related technology in the pharmaceutical/biotechnology industry preferred - Knowledgeable in Good Clinical Practices, and FDA regulations necessary - Excellent time management and organization skills required - Must have sound problem resolution, judgment, and decision:
making abilities - Must be able to work well in a team:
based environment with minimal supervision Job
Summary:
Key Responsibilities include:
- Lead study level system requirements meetings with internal and external clients - Design and oversee the development of study specific technical documents - Document possible risk and implement mitigation plans - Manage project related timelines and associated activities Functional Analyst, Clinical Development, Quality, GCP, GMP, FDA, Vendor, EDC Source:
http:
//www.
tiptopjob.
com/jobs/29791366_job.
asp?source=trovit.
Estimated Salary: $20 to $28 per hour based on qualifications.
Job Description:
Technical Analyst :
23434 Bachelor's Degree in life science, computer science, engineering, business or related discipline - 4 or more years of experience in clinical operations, clinical development or clinical quality assurance - Experience implementing clinical systems, such as CTMS, EDC, IVRS, ePRO or other related technology in the pharmaceutical/biotechnology industry preferred - Knowledgeable in Good Clinical Practices, and FDA regulations necessary - Excellent time management and organization skills required - Must have sound problem resolution, judgment, and decision:
making abilities - Must be able to work well in a team:
based environment with minimal supervision Job
Summary:
Key Responsibilities include:
- Lead study level system requirements meetings with internal and external clients - Design and oversee the development of study specific technical documents - Document possible risk and implement mitigation plans - Manage project related timelines and associated activities Functional Analyst, Clinical Development, Quality, GCP, GMP, FDA, Vendor, EDC Source:
http:
//www.
tiptopjob.
com/jobs/29791366_job.
asp?source=trovit.
Estimated Salary: $20 to $28 per hour based on qualifications.
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