top of page

Careers at NuvOx

Clinical Operation Specialist

The prospective Clinical Operation Specialist will be a member of the Clinical Operations team which is responsible for the day to day planning, execution and management of clinical trials.

Responsibilities

  • Provide support to the Clinical Operations Department

  • Review regulatory documents for accurate content

  • Contribute to the development of clinical documents

  • Provide oversite of document version tracking and filing

  • Perform investigator file reviews and logging of outstanding issues

  • Attend meetings and teleconferences and generate and distribute agendas and minutes

  • Oversee essential document management during all study phases

  • Ensure clinical trials are conducted according to regulations and good clinical practices

  • Assist in coordination and tracking of Investigator and third-party payments.

  • Other study related tasks as required

Job Requirements

  • Minimum of a bachelor’s degree in a scientific or health care discipline preferred

  • Prior experience in pharmaceutical or biotech industry

  • Minimum experience 4 years supporting clinical trials

  • Highly effective team player with exceptional interpersonal skills building relationships with clinical trial sites

  • Ability to work independently with little oversight and attention to detail and results oriented

  • Ability to utilize critical thinking to analyze problems which may require multiple factors and approaches

  • Sound judgement and problem solver – know when to escalate, report and make good decisions based on business objectives.

  • Excellent oral and written communication skill

  • This position requires some travel

We hope this is the environment that you are looking for and let’s connect! Please send an email to accounting@nuvoxpharma.com with your resume and CV. Thank you. 

bottom of page