Research Associate

sidekick 2. Nov 2020 Fullt starf

A Research Associate at SidekickHealth will be overseeing clinical studies and study-related projects. As a Research Associate, you will create and write study protocols, conduct regular site visits, manage study-related communications, and prepare interim and final reports. You will play a leading role in generating and overseeing study procedures, study timelines, documentation, and records. You should be able to quickly identify logistical problems and initiate appropriate solutions in a collaborative, multi-disciplinary environment.


  • Create and write study protocols
  • Present protocols to collaborators and other internal and external stakeholders
  • Identify, evaluate and establish study collaborations and KOL relationships
  • Train study staff on therapeutic areas, protocol requirements and study documentation
  • Write and facilitate ethics and other regulatory applications and approvals
  • Protect participants´ confidentiality and updating regulatory information
  • Conduct regular site visits as needed, coordinating project meetings and writing meeting notes and reports
  • Ensure compliance with standard operating procedures and data protection guidelines
  • Conduct statistical analysis of data sets
  • Assist with data analysis, manuscript reading and writing
  • Supervise research assistants assigned to various research tasks, when applicable
  • Other tasks and responsibilities as needed


  • Master´s degree in biomedical sciences or a related field
  • A minimum of 2-5 years experience in a research-related role
  • Healthcare experience a plus
  • Excellent knowledge of medical and/or behavioral intervention research and methodology
  • Familiarity with clinical research regulations and practical implementation
  • Strong verbal and communication skills
  • Strong English and Icelandic language proficiency

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If you believe your skills and experience fit the job description and you have passion for our mission, please get in touch.