Careers at NuvOx

Clinical Operation Specialist

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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.

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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

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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.