Pharmacovigilance Associate II

Brisbane, CA 94949 | Contract

Post Date: 03/30/2018 Job ID: 12800 Industry: Clinical & Scientific

Bayside Solutions  is seeking a Pharmacovigilance Associate II to be part of our Client’ s team in Marin County. This is an opportunity to work with a local Biopharmaceutical company focusing on the developing and commercializing novel therapies for rare diseases. 

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. Their company has been recognized as one of the fastest drug developers in the industry and has also been recognized among the Top 10 World’ s Most Innovative Company’ s in 2015 & 2016.Their organization is fueled by their employee’ s passion and dedication to change the course of disease.

Our Company Bio: Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Pharmacovigilance Associate II

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop and commercialize novel drugs for treating rare diseases.
  • Work for a company that is local to the bay area and recognized as a leader of innovation. 
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Participates in activities related to, and processing of, Adverse Events for marketed products and investigational products.
  • Accountable for accurate data capture for individual case safety reports.
  • Responsible for narrative creation for individual case safety reports.
  • Perform quality review and submissions (as appropriate).
  • Ensuring departmental workflow processes and timelines are followed.
  • Proactively managing workload to ensure regulatory timelines are met.
  • Demonstrated knowledge of safety concepts and global regulatory reporting obligations

Required Qualifications:
  • Bachelor' s degree in a Life Science Degree Required
  • Minimum of 2-5 year previous Pharmacovigilance experience required.
  • Strong knowledge of medical terminology.
  • Strong organizational skills, detail oriented, ability to adapt to change.
  • Proven team player with the ability to function in a multi-disciplinary environment.
  • Demonstrates initiative and accountability.
  • Excellent communication skills, both verbal and written.
  • Computer literate

 

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