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June

Medical Monitor

Novotech - Brisbane Grove, NSW

Health, Medical & Pharmaceutical
Source: uWorkin

JOB DESCRIPTION

Medical Monitor

Novotech is internationally recognized as the leading regional full-service contract research organization (CRO) in Asia-Pacific providing clinical development services across all clinical trial phases and therapeutic areas, including an in-house and integrated global product development and regulatory affairs consultancy, BioDesk.

Working in a fast paced and adaptable environment, we set a high benchmark for clinical trial operations by listening carefully, allocating Asia Pacific’s best people and talent, and leveraging best in class platforms, technology, systems and processes to meet our client’s clinical program goals and ultimately improve patient lives.

Our people are critical in meeting organisational and client’s objectives and we place a strong emphasis on creating an inclusive, collaborative, transparent and collegiate work environment where everyone is supported to be the best they can be. We support our employees with financial assistance to enable flexible working arrangements, paid parental leave for primary and secondary careers, and regular training, learning, and international knowledge-sharing opportunities.

Due to continued growth, we are looking for an experienced Medical Monitor to join the Medical Services team based in Australia.

Responsibilities

  • Provide medical oversight for Novotech sponsored clinical trials, acting as medical representative to the Novotech project team.
  • Prepare a Medical Monitoring Plan for each study according to project scope and provide medical review and commentary on client protocol and/or Investigator Brochure.
  • Attend Investigator Meeting; prepare and present safety or medical aspects if required.
  • Provide medical review and input to Clinical Monitoring Plan and Safety Management Plan as required and provide medical review, comment and assessment of causality for Serious Adverse Events (SAEs) occurring in Novotech sponsored clinical trials.
  • Follow up any medically oriented safety or protocol related questions or queries directly with the Investigator as required.
  • Provide ad hoc medically oriented protocol advice to Investigators.


Experience
  • Medically qualified with experience in clinical practice.
  • Experience in drug development, pharmacovigilance in the pharmaceutical and/or CRO industry
  • Knowledge of drug safety reporting requirements and practice.
  • Excellent verbal and written communication skills are essential
  • Proactivity, adaptability, team work and collaboration are essential


Find out more about working at Novotech at: www.novotech-cro.com/careers

Novotech is committed to offering Equal Employment Opportunities (EEO) where everyone has equal access to employment opportunities based on merit, without fear of discrimination or harassment.

Brisbane Grove, NSW

Health, Medical & Pharmaceutical




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