Drug Safety Associate (NON-HCP) Job
Company Name:
Arca24.com
Salary period: Annual
Drug Safety Associate needed for a contract opportunity with Yoh's client located in South San Francisco, CA.
What You'll Be Doing:
- Demonstrated knowledge of safety concepts, per ICH and FDA guidelines per drug safety reporting requirements.
- Performs a review of ancillary documentation accompanying ICSR reports and identifies pertinent clinical information for incorporation into the case narrative.
- Performs Data Capture and Quality Review for all molecules and serves as a back up for additional projects.
- Identifies and initiates requests for case follow up for clinical trials and post marketing adverse events.
- Works with Submissions Team Responsible to properly identify US regulatory reporting requirements.
- Demonstrates a general understanding of appropriate labeling documents for assigned project(s).
- Demonstrates knowledge and understanding of safety exchange agreements (if applicable).
- Participates on Study Management Teams (as applicable) Assists in the development of drug safety presentation for investigator meeting presentations.
- Assists in clinical trial reconciliation process (as applicable).
- Organizes work load to ensure compliance with regulatory timelines for ICSR reporting.
- Ensures departmental workflow processes and timelines are followed.
What You Need to Bring to the Table:
- BA/BS degree requirement
- Minimum two (2) years of clinical experience in a health care related field
- Computer proficiency and data entry experience preferred
- Excellent communication skills, both written and verbal
- Previous experience in Drug Safety (preferred)
Opportunity is Calling, Apply Now!
Recruiter: Krista Leach
Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer, M/F/D/V.
J2W: SCIENTIFIC; J2W: CLINICAL
MONJOB
J2WSWSCI
Ref:
SFSF: LSEstimated Salary: $20 to $28 per hour based on qualifications.
Arca24.com
Salary period: Annual
Drug Safety Associate needed for a contract opportunity with Yoh's client located in South San Francisco, CA.
What You'll Be Doing:
- Demonstrated knowledge of safety concepts, per ICH and FDA guidelines per drug safety reporting requirements.
- Performs a review of ancillary documentation accompanying ICSR reports and identifies pertinent clinical information for incorporation into the case narrative.
- Performs Data Capture and Quality Review for all molecules and serves as a back up for additional projects.
- Identifies and initiates requests for case follow up for clinical trials and post marketing adverse events.
- Works with Submissions Team Responsible to properly identify US regulatory reporting requirements.
- Demonstrates a general understanding of appropriate labeling documents for assigned project(s).
- Demonstrates knowledge and understanding of safety exchange agreements (if applicable).
- Participates on Study Management Teams (as applicable) Assists in the development of drug safety presentation for investigator meeting presentations.
- Assists in clinical trial reconciliation process (as applicable).
- Organizes work load to ensure compliance with regulatory timelines for ICSR reporting.
- Ensures departmental workflow processes and timelines are followed.
What You Need to Bring to the Table:
- BA/BS degree requirement
- Minimum two (2) years of clinical experience in a health care related field
- Computer proficiency and data entry experience preferred
- Excellent communication skills, both written and verbal
- Previous experience in Drug Safety (preferred)
Opportunity is Calling, Apply Now!
Recruiter: Krista Leach
Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer, M/F/D/V.
J2W: SCIENTIFIC; J2W: CLINICAL
MONJOB
J2WSWSCI
Ref:
SFSF: LSEstimated Salary: $20 to $28 per hour based on qualifications.
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