Research Scientist - (Part-time or Consultant)
Clinical Research Management - Frederick, MD

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Growing and well-respected biomedical (clinical, basic and applied) research firm is hiring. If you are passionate about research, and are looking for a firm that shares your passion, and provides competitive salaries with a strong benefits package, join the ClinicalRM team.

We are currently seeking a Research Scientist - Consultant for the Frederick, MD area to work on a Part-time or consultant basis up to 20 hours per month .

This position has the ability to work from a remote location while reporting to the actual work facility one time per quarter or as needed.

RESPONSIBILITIES:

  • Provide guidance on the design and interpretation of commonly used in vivo assays such as pK and other delivered by research service contractors. They shall be asked for input on the project endpoints and milestones.

  • Evaluate and provide feedback on project strategies from the perspective of FDA requirements and regulations. Expected to provide feedback and guidance on projects and guidance on projects through conference call and by email. Travel only as necessary to be onsite.

  • Provide analytical reports for each compound and animal model within 2 weeks of receiving the data followed by suggested technical guidelines for proceeding with the project using FDA guidelines for candidate submission within 2 weeks of the data analysis.

  • Maintain a safe workplace ensuring that he/she is aware of and observes appropriate safety and occupational health rules and regulations. Employee is required to attend safety training relative to his/her position and report any infractions of safety procedures to the facility Safety Officer.

  • Performs light duties and other related duties as required and assigned.

  • MINIMUM QUALIFICATIONS:

  • Position requires a PhD with 20+ years of experience.

  • Should have prior experience developing and transitioning small molecules into animal models and human clinical studies. Ideally, candidate should have experience as Study Director on small molecule drug development for IND, Phase I, II, and III FDA submissions.

  • Experience with pK and Toxicity studies are needed.

  • Ability to work from remote location and possess the tools necessary to do so (i.e. phone, computer, email, etc.)

  • Ability to travel to the worksite at minimum one time per quarter.

  • Must be a US Citizen to comply with facility requirements.

  • Must be able to work independently following a brief period of specific technical training.

  • Qualified candidates will receive consideration for employment without regard to race, color, religion, sex, or national origin. Candidates for positions under ClinicalRM’s contracts with the Department of Defense (DoD) will be required to pass one or more background/security investigations conducted by the DoD, U.S. Army, or other Federal Government agency. Such investigations may include criminal records and credit history checks.

    ClinicalRM is an Affirmative Action-Equal Opportunity Employer

    www.clinicalrm.com

    Clinical Research Management - 18 months ago - save job - block
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