Protocol Specialist/Technical Writer
Clinical Research Management - Hinckley, OH

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Growing and well-respected biomedical (clinical, basic and applied) research firm has openings at Clinical RM Headquarters . 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 part-time (30 hrs/week) Protocol Specialist/Technical Writer for the Hinckley, Ohio area.

RESPONSIBILITIES:

  • Writing and editing assigned concept proposals and/or clinical study protocols for Sexually Transmitted Infections, related diagnostics and epidemiology.
  • Participate in project team meetings to provide input regarding deliverables, timelines, and processes.
  • Conducting literature searches for specific projects and topics.
  • Conducting interviews and/or meets with STI Scientific Concept Committee members and subject matter experts, as appropriate, on the relevant subject to gather and collect material for writing.
  • Formatting and managing documents with multiple review cycles and tight deadlines.
  • Routing documents for approval.
  • Assisting with SOP development and review.
  • Proofreading and editing written material for punctuation, grammatical, and spelling errors.
  • Integrating best practices and procedures in writing and producing effective write-ups.
  • Writing, preparing, and designing fact sheets, brochures, web pages, directories, and related content for the ClinicalRM STI Clinical Trials Group (CTG) as needed.
  • Estimated 30 hours/week, May work remotely
  • Performs light duties and other related duties as required and assigned
  • MINIMUM QUALIFICATIONS:


  • Master’s degree or PhD in Life Sciences, with experience in Infectious Diseases preferred.
  • Documented clinical research experience including protocol development and protocol writing.
  • Ability to accomplish assignments independently.
  • Skilled in presenting highly technical and scientific information that maintains scientific accuracy and at the same time adjusts the level of writing to the understanding of the intended audience.
  • Familiar with government proposal process preferred.
  • Familiar with clinical research industry preferred.
  • Ability to multi-task and work with changing priorities.
  • Flexible hours to be able to work during normal business hours, with some after hours work required to meet proposal deadlines and subject matter experts’ timelines.
  • Strong written and verbal communication skills.
  • Must be highly organized with the ability to prioritize and meet deadlines.
  • Demonstrate ability to interrelate with all levels of the user community.
  • Required Knowledge, Skills and Abilities: knowledge of applicable highly complex office procedures and techniques relating to position.
  • 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

    “NorthCoast 99” Best Places to Work recipient

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