The Clinical Process Compliance Associate is an independent contributor who assists the Quality Control Compliance and/or Metrics team with the oversight of clinical trial activities based on the standards required to ensure adherence to GCP and AbbVie procedures. They are aware of both internal and external business environment requirements and escalate issues to management and develops scenarios for issue resolution.
Responsibilities:
- Responsible for compliance with applicable Corporate and Divisional policies and procedures.
- Assists in the completion of activities regarding quality control compliance investigational product release for clinical studies and/or data collection; including working with functional areas to ensure assigned activities are completed per plan.
- Communicates clinical-related information and escalates issues to management with possible resolutions
- Maintains the SharePoint site and other systems required to support functional activities.
Qualifications :
Minimum Qualifications:
- Bachelors degree (or equivalent ex-US) is required typically in nursing or scientific field. An Associates degree/R.N. (or equivalent ex-US) with relevant experience is acceptable.
- 2 years Pharma-related/clinical research related experience
- Experience applying standard business procedures (SOPs ICH Global Regulations Ethics and Compliance).
Preferred Qualifications:
Other Required Skills:
- Demonstrates analytical and critical thinking skills.
- Possesses good communication skills.
Additional Information :
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location and we may ultimately pay more or less than the posted range. This range may be modified in the future.
We offer a comprehensive package of benefits including paid time off (vacation holidays sick) medical/dental/vision insurance and 401(k) to eligible employees.
This job is eligible to participate in our short-term incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount is earned vested and determinable. The amount and availability of any bonus commission incentive benefits or any other form of compensation and benefits that are allocable to a particular employee remains in the Companys sole and absolute discretion unless and until paid and may be modified at the Companys sole and absolute discretion consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
Work :
No
Employment Type :
Full-time
The Clinical Process Compliance Associate is an independent contributor who assists the Quality Control Compliance and/or Metrics team with the oversight of clinical trial activities based on the standards required to ensure adherence to GCP and AbbVie procedures. They are aware of both internal and...
The Clinical Process Compliance Associate is an independent contributor who assists the Quality Control Compliance and/or Metrics team with the oversight of clinical trial activities based on the standards required to ensure adherence to GCP and AbbVie procedures. They are aware of both internal and external business environment requirements and escalate issues to management and develops scenarios for issue resolution.
Responsibilities:
- Responsible for compliance with applicable Corporate and Divisional policies and procedures.
- Assists in the completion of activities regarding quality control compliance investigational product release for clinical studies and/or data collection; including working with functional areas to ensure assigned activities are completed per plan.
- Communicates clinical-related information and escalates issues to management with possible resolutions
- Maintains the SharePoint site and other systems required to support functional activities.
Qualifications :
Minimum Qualifications:
- Bachelors degree (or equivalent ex-US) is required typically in nursing or scientific field. An Associates degree/R.N. (or equivalent ex-US) with relevant experience is acceptable.
- 2 years Pharma-related/clinical research related experience
- Experience applying standard business procedures (SOPs ICH Global Regulations Ethics and Compliance).
Preferred Qualifications:
Other Required Skills:
- Demonstrates analytical and critical thinking skills.
- Possesses good communication skills.
Additional Information :
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location and we may ultimately pay more or less than the posted range. This range may be modified in the future.
We offer a comprehensive package of benefits including paid time off (vacation holidays sick) medical/dental/vision insurance and 401(k) to eligible employees.
This job is eligible to participate in our short-term incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount is earned vested and determinable. The amount and availability of any bonus commission incentive benefits or any other form of compensation and benefits that are allocable to a particular employee remains in the Companys sole and absolute discretion unless and until paid and may be modified at the Companys sole and absolute discretion consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
Work :
No
Employment Type :
Full-time
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