Triage Manager Job
Company Name:
Yoh
Triage
manager
job
Triage Manager needed for a contract opportunity with Yoh's client located in Ridgefield, CT. The Big Picture - Top Skills You Should Possess:- Clinical Safety - IND NDA Reporting - Adverse
events
What You'll Be Doing:- Directly responsible for ensuring that adverse events are processed, analyzed and reported according to Corporate SOPs, local working instructions and local regulatory requirements. - Responsible for distribution and retrieval of data to internal and external customers as needed for analysis and compliance with regulations. - Serve as point of contact with clinical team in areas of adverse events process. - Assist with collection, processing, and reporting on adverse event reports. What You Need to Bring to the Table:- Bachelor's degree in biomedical science or equivalent and a basic knowledge of clinical medicine. - Pharmaceutical Industry experience. - Must have three to five (3 - 5) years of experience in processing clinical safety data in industry setting or the equivalent. - Must possess solid understanding of federal regulations as they apply to drug surveillance for both IND and NDA reporting. Bonus Points! Otherwise Known As Preferred
Qualifications:- Strong communication skills required in order to facilitate report preparation, participate in working groups and interact with a variety of departments. - Experience with computerized data entry and retrieval as well as other
computer
based applications (Word/Excel) is also required. Opportunity is Calling, Apply Now! Recruiter: Chelsea Tevis Yoh, a Day and Zimmermann company, is an Equal Opportunity Employer, M/F/D/V. J2W: SCIENTIFIC; J2W: CLINICAL MONJOBJ2WNECLIN Ref: SFSF: LS MYK62683JREstimated Salary: $20 to $28 per hour based on qualifications.
Yoh
Triage
manager
job
Triage Manager needed for a contract opportunity with Yoh's client located in Ridgefield, CT. The Big Picture - Top Skills You Should Possess:- Clinical Safety - IND NDA Reporting - Adverse
events
What You'll Be Doing:- Directly responsible for ensuring that adverse events are processed, analyzed and reported according to Corporate SOPs, local working instructions and local regulatory requirements. - Responsible for distribution and retrieval of data to internal and external customers as needed for analysis and compliance with regulations. - Serve as point of contact with clinical team in areas of adverse events process. - Assist with collection, processing, and reporting on adverse event reports. What You Need to Bring to the Table:- Bachelor's degree in biomedical science or equivalent and a basic knowledge of clinical medicine. - Pharmaceutical Industry experience. - Must have three to five (3 - 5) years of experience in processing clinical safety data in industry setting or the equivalent. - Must possess solid understanding of federal regulations as they apply to drug surveillance for both IND and NDA reporting. Bonus Points! Otherwise Known As Preferred
Qualifications:- Strong communication skills required in order to facilitate report preparation, participate in working groups and interact with a variety of departments. - Experience with computerized data entry and retrieval as well as other
computer
based applications (Word/Excel) is also required. Opportunity is Calling, Apply Now! Recruiter: Chelsea Tevis Yoh, a Day and Zimmermann company, is an Equal Opportunity Employer, M/F/D/V. J2W: SCIENTIFIC; J2W: CLINICAL MONJOBJ2WNECLIN Ref: SFSF: LS MYK62683JREstimated Salary: $20 to $28 per hour based on qualifications.
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