Connexion Systems + Engineering
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Caroline Driscoll
Pharmacovigilance Specialist
Job Description
Connexion’s mission is to provide "best in class" services to job seekers. We strive to achieve excellence in job placement, staffing, and recruiting services, while treating candidates with the professionalism and respect they deserve.
Title: Pharmacovigilance Specialist
Hiring Organization: Connexion Systems & Engineering
Compensation, Benefits, and Employment Type
Description:
Provides operational support for global pharmacovigilance activities of marketed products. Ensures pharmacovigilance deliverables are of the highest quality and meet global regulatory reporting timelines. Responsible for data review, compilation, and analysis, including management of the integrated safety database.
Primary responsibilities for the role:
Please use the apply button to submit your resume for consideration. A Connexion Representative will contact you shortly.
You may also send your resume and cover letter via email to the recruiter listed below. You MUST include the Job# and Job Title in your subject line.
If you are active in a job search but this job is not for you, please reach out to jobpostings@csetalent.com. We would be glad to help you find the perfect job!
Title: Pharmacovigilance Specialist
Hiring Organization: Connexion Systems & Engineering
Compensation, Benefits, and Employment Type
- Duration: 12-month contract position
- Pay rate: $40-$50.48/hr
- Job Location: Los Angeles, CA -or- Remote, US
- Schedule: flexible, standard business hours
- Job#: bh17274
Description:
Provides operational support for global pharmacovigilance activities of marketed products. Ensures pharmacovigilance deliverables are of the highest quality and meet global regulatory reporting timelines. Responsible for data review, compilation, and analysis, including management of the integrated safety database.
Primary responsibilities for the role:
- Management of Adverse Events including activities such as processing adverse event case reports and conducts follow-up.
- Notifies regulatory agencies and business partners accordingly; responds to requests from regulatory agencies.
- Reviews scientific literature and bibliographic sources; draft and manage periodic safety update reports.
- Evaluates safety profiles; draft and manage signal detection reports; ensures document filing and archiving.
- Participation in the processes of involving the collection, processing, review and distribution of adverse event information regarding development and marketed pharmaceutical products.
- Contributes to ensure compliance of pharmacovigilance activities including activities such as conduct case reconciliation with concerned departments, affiliates, distributors or business partners.
- Take part in self-inspection visits, audits, inspections and in CAPAs management, create or update pharmacovigilance procedures and working practices
- Provide training to concerned persons based on the training plan and managing training documentation; archive documents according to prevailing standards.
- Support in the procedures of global pharmacovigilance operations such as Standard Operation Procedures (SOPs), internal business practices or working instructions.
- Serves in an advisory capacity including activities such as product monographs review, draft responses to pharmacovigilance requests from regulatory agencies; participates in the drafting and implementation of pharmacovigilance contracts and agreements.
Please use the apply button to submit your resume for consideration. A Connexion Representative will contact you shortly.
You may also send your resume and cover letter via email to the recruiter listed below. You MUST include the Job# and Job Title in your subject line.
If you are active in a job search but this job is not for you, please reach out to jobpostings@csetalent.com. We would be glad to help you find the perfect job!
Meet Your Recruiter
Caroline Driscoll
Account Manager & Sr. Technical Recruiter
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