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Welcome to Salamandra

Salamandra provides strategic, technical, and regulatory consulting services to the pharmaceutical industry for drug, biologic, and device development.  Our in-house experts, as well as a wide network of subject matter experts, are prepared to support your company in the areas of chemistry, manufacturing, and controls (CMC), nonclinical and early phase development, and Phase 1-4 clinical development.

  • 301-652-6110
  • 1-301-652-6110
  • 4800 Hampden Lane, Suite 900
    Bethesda, MD 20814-2998

Our Location

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Phone: 301-652-6110 Fax: 1-301-652-6739

Salamandra is currently seeking entry-level candidates to fill our Research Assistant position.  See below for more information.

Our Professional Team is Our Greatest Asset

Are you interested in regulatory consulting work?  Do you have experience working in the pharmaceutical industry?  Are you educated in a life-science field?  Salamandra is proud of its diverse team of dedicated professionals and we often seek qualified individuals to help maintain the high standard of our company.

Pursue a life-sciences career

With competitive benefits, a pleasant, professional downtown office, and our culture of promoting professional growth, we believe Salamandra provides a great opportunity to either start or continue a successful career in the regulatory environment.

Competitive Salary

Paid TIme Off

Holiday | Sick | Vacation

Health Benefits

401(k) Retirement Plan

Salamandra is currently seeking entry-level candidates to fill our Research Assistant position.

  • Primary Responsibilities and Duties

    Specific responsibilities of this position include, but are not limited to:
    • Supporting senior staff in research and analysis by conducting literature searches, reviewing publications, researching precedent, and preparing summaries of findings
    • Researching regulations and guidance documents concerning a particular topic and summarizing the findings
    • Preparing written or tabular summaries of data from publications or study reports to be included in technical documents for submission to regulatory authorities
    • Document organization, compilation, and electronic production
    • Performing quality control review of documents prepared by the Salamandra team
    It should be noted that this is not a laboratory position nor is there a laboratory on site.
  • Success Factors

    Successful performance in this role requires the ideal candidate to be:
    • Able to quickly learn new skills and proactively ask questions while working on deliverables with moderate supervision
    • Exceptionally detail-oriented as accuracy is essential
    • Clear and effective in oral and written communication, with a good command of English grammar, usage, and writing conventions
    • Self-motivated and continually seeking ways to enhance contribution to the team
    • Able to analyze information to draw logical conclusions and to apply multiple perspectives to facilitate complex problem-solving
  • Job Qualifications

    • Bachelor’s degree and an interest in the life sciences and/or public health are required. Related drug development and/or regulatory experience is a plus
    • Good communication, interpersonal and organizational skills are necessary to facilitate working in a small-group technical environment
    • Prior experience with reviewing scientific literature, writing scientific documents, and organizing and analyzing data would be highly valued
    • In depth familiarity with the advanced features of the Microsoft Office applications suite is expected
    • Authorization to work in the US without time limitations

We are proud to be an Equal Employment Opportunity employer. We celebrate the diversity of our employees and all employment decisions are made based on qualifications, merit, and business need.  Candidates may forward their resume via the Contact Us page.

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