Accelerating clinical research to bring new treatments to patients faster.

Employment opportunities

Employment opportunities

Impact is always looking for exceptional talent for individuals committed to excellence in clinical research. If you are looking for a challenging opportunity with career growth potential in clinical research, submit your information below.

Medical Writer & Consultant

Functions/Responsibilities

  • Oversees the development of protocols, Informed Consent Forms, and amendments. Including managing project timelines, drafting, editing, coordinating review cycles, adjudicating reviewer comments, and overseeing publishing,  and finalization
  • Acts as a key strategic thinking partner for team members on protocol development and the above deliverables
  • Actively keeps team members apprised of projects and timelines

Who you are

  • 2 years or more years of medical writing and/or clinical project management experience, preferably in the biotech/Pharmaceutical industry
  • Masters or PhD degree in the biological sciences or liberal arts preferred or equivalent experience
  • Knowledge of clinical trial processes, regulatory requirements, and industry guidelines.

Capabilities

  • Superb written and oral communication skills, with a proven ability to communicate effectively with all levels in the organization
  • Demonstrated experience in clinical and nonclinical document preparation and finalization
  • Strong project management and team facilitation skills
  • Team player with demonstrated strong interpersonal skills and ability to build effective working relationships throughout all levels of the organization
  • Strong analytical, problem-solving, and consulting skills, with the ability to work independently and collaboratively.
  • Strong planning and organizational skills, including ability to prioritize and organize high volume workflow ensuring attention to detail, and highest level of accuracy within required timeframe

Please submit a simple text resume below.
Thank you!

OUR EXPERT TEAM

At Impact Clinical Research, our expert team excels in

MEDICAL WRITING

Impact writers have extensive experience supporting clinical documents from IND submission through post-marketing commitments.

MONITORING SERVICES

Impact offers comprehensive clinical trial monitoring and site management services from feasibility through site closeout to support clinical trials.

PROJECT MANAGEMENT

Impact project managers are highly skilled, experienced and integrate seamlessly with your team in order to deliver high quality, effective support.

At Impact, experienced people work together to deliver outstanding results.

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