Drug Safety, Triage Manager Job
Company Name:
Arca24.com
Salary period: Annual
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 & Zimmermann company, is an Equal Opportunity Employer, M/F/D/V. Click here to contact us if you are an individual with a disability and require accommodation in the application process.
J2W: SCIENTIFIC; J2W: CLINICAL
MONJOB
J2WNECLIN
Ref:
SFSF: LSEstimated Salary: $20 to $28 per hour based on qualifications.
Arca24.com
Salary period: Annual
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 & Zimmermann company, is an Equal Opportunity Employer, M/F/D/V. Click here to contact us if you are an individual with a disability and require accommodation in the application process.
J2W: SCIENTIFIC; J2W: CLINICAL
MONJOB
J2WNECLIN
Ref:
SFSF: LSEstimated Salary: $20 to $28 per hour based on qualifications.
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