Student Veterans of America Jobs

Welcome to SVA’s jobs portal, your one-stop shop for finding the most up to date source of employment opportunities. We have partnered with the National Labor Exchange to provide you this information. You may be looking for part-time employment to supplement your income while you are in school. You might be looking for an internship to add experience to your resume. And you may be completing your training ready to start a new career. This site has all of those types of jobs.

Here are a few things you should know:
  • This site is mobile friendly. You do not need a log-in or password to access information.
  • Jobs on this site are original and unduplicated and come from three sources: the Federal government, state workforce agency job banks, and corporate career websites. All jobs are vetted to ensure there are no scams, training schemes, or phishing.
  • The site is refreshed daily to remove out-of-date content.
  • The newest jobs are listed first, so use the search features to match your interests. You can look for jobs in a specific geographical location, by title or keyword, or you can use the military crosswalk. You may want to do something different from your military career, but you undoubtedly have skills from that occupation that match to a civilian job.
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Job Information

System One Services Pharmacovigilance Scientist I in Basking Ridge, New Jersey

Pharmacovigilance Scientist IBasking Ridge, New Jersey

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Type:Contract

Category:Scientific & Clinical

Job ID:219984

Date Posted:05/04/2021

Title: Pharmacovigilance Scientist I

Location:Basking Ridge, NJ

Start date:ASAP

Responsibilities:

Max Subs: 3

Duties:

The Scientist Pharmacovigilance main role is to process and evaluate adverse events (AEs) received from clinical trials and/or postmarketing sources to support drug development and ensure safety and efficacy of Daiichi Sankyo products. This includes data collection, entry, evaluation, follow up, and distribution in a timely fashion to ensure compliance with local and global regulatory reporting.

Skills:

Delivers high quality work, assesses individual and vendor/CRO work with minimal supervision. Executes strategic plans within multiple projects and can prioritize in accordance with strategy. Competent in identifying and understanding issues independently and can contribute to remediation plans Competent knowledge of pharmacology, clinical research and medical terminology, global data entry conventions and systems and procedures for application in daily work. Communicates effectively with team/project members using clear and effective verbal and written communication skills Effectively manages own workload to meet multiple deadlines in a timely manner. Understands functional role and others’ functional roles within the clinical trial process.

Education:

Bachelor’s degree in nursing, pharmacy, or healthcare related field with minimum of two (2) years of PV experience and knowledge of FDA regulations.

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