NOVOTECH - Datatronic

Brief Position Description:
The Clinical Contracts Specialist (CC Specialist) is responsible for the timely development of investigator grants and Clinical Trial Agreement templates during the start-up stage of a Clinical Trial. The CC Specialist will work closely with Project Management, Clinical Operations, Legal teams, and the client to ensure finalisation of approved site budgets and execution of approved site Clinical Trial Agreements. The ideal candidate will be professional, analytical and possess excellent written and verbal communication skills

Minimum Qualifications & Experience:

• Bachelor's Degree in a relevant field (science, law or other).
• Minimum 3 years' experience in the clinical trials industry including experience in contract and budget negotiation.
• Understanding of business/financial concepts used in clinical trials.
• Excellent communication and interpersonal skills. Good organisational skills;
  positive team player; attention to detail.

Responsibilities:

Contracts

• Understand which Clinical Trial Agreement template is used by countries in
  Novotech geographies; and where site specific templates are applicable.
• Independent review and amendment of Clinical Trial Agreements within agreed
  negotiation parameters and policies.
• Escalate Clinical Trial Agreements outside of agreed negotiation parameters and
  policies as required; and obtain guidance and approval by Legal for any
  deviations.
• Work closely with Project Management, Clinical Services, Finance and Legal teams to facilitate timely execution of site Clinical Trial Agreement.
• Serve as country point person for their country/region regarding Clinical Trial
  Agreements.

Budgets

• Develop the investigator grant (country master budget) using industry standard
  systems.
• Review the study protocol to ensure protocol assessments are included and
  consult with Clinical Services Team to confirm completeness of the budget.
• Ensure industry standard of care concepts are incorporated into the budget and
  in line with Fair Market Value.
• Escalate site budgets outside of agreed negotiation parameters as required and
  obtain guidance and approval by client for any deviations.
• Any other tasks as assigned by Line Manager.

Novotech is proud to offer a great workplace. We are committed to being an employer of choice for gender equality and providing an inclusive work environment where everyone is treated fairly and with respect.

Our team members are passionate about what we do, but we understand work is only one of the things that is important to them. We support our team members with flexible working options, paid parental leave for both parents, flexible leave entitlements, wellness programs and ongoing development programs.

We are looking for people who are passionate about working clinical research and biotech, including people who identify as LGBTIQ+, have a disability or have caring responsibilities.

We are a Circle Back Initiative Employer and commit to respond to every application. We look forward to contacting you regarding your application.