CAREERS

Clinical Operation Manager - Job Code: CL-2021009

Currently we are looking for a Clinical Operation Manager, with experience in delivering interventional cross-functional clinical trials to join our team!

The Clinical Operation Manager is responsible for driving our clinical operation excellence by focusing on project delivery, productivity and quality for complex, full service clinical studies.

Primary responsibilities:

  • Operationalize RFP requirements and support the development of business/financial proposals
  • Contribute to the development of efficient and innovative study design to support project objectives
  • Oversee the execution of clinical projects while optimizing speed, quality and cost of delivery, present project information proactively to all stakeholders
  • Set project objectives according to agreed strategy, effectively communicate and assess performance while suggesting ways of improvement
  • Ensure resource planning, standard setting, performance management and evaluation
  • Collaborate with other operational departments within the company where necessary to support milestone achievement
  • Ensure project quality by identifying quality risks, responding to issues raised by project team and implementing appropriate corrective and preventative action plans
  • Direct, lead and motivate the team to ensure a high standard of professionalism, efficiency, effectiveness and innovation in the delivery of projects
  • Ensure compliance with internal processes and regulatory requirements across clinical services, while contributing to the ongoing update/development and implementation of clinical SOPs
  • Identify training needs where necessary, contributing to the design and implementation of education and training to meet the requirements of the projects/service
  • Manage invoicing process while overseeing service budget. Monitor and reconcile income and expenditure statements while identifying opportunities to accelerate activities and bring revenue forward


Qualifications:  

  • University Degree and Master’s Degree (or Ph.D. or MD) in health or biological sciences, pharmacology, medicine or chemistry
  • Minimum of 7 years of clinical experience in the Pharmaceutical or CRO including 4 years of demonstrated experience in clinical trials management
  • Therapeutic knowledge in at least 2 of the areas: Oncology, Hematology, CNS, Rare Diseases
  • Expertise with ICH/GCP and regulatory guidelines pertaining to the conduct of clinical trials on human subjects
  • Solid understanding of the drug development process, pharmaceutical legislation and scientific matters
  • Excellent organizational and prioritization skills and ability to develop, plan and implement short and long-range goals
  • Ability to supervise and train staff, including organizing, prioritizing and scheduling work assignments
  • Team building, leadership, communication and mentoring skills
  • Advanced critical thinking and problem-solving skills and ability to take appropriate corrective action
  • Finance and budgeting knowledge
  • Advanced oral and written communication and interpersonal skills (including experience in making presentations at conferences, meetings and training sessions).
  • Excellent command (written and verbal) of English language and proficient knowledge of medical terminology
  • IT literacy (MS Windows, MS Office, Internet Use)
  • Driving license
  • Availability to travel throughout Greece and abroad (up to 30% of time) with little prior notice

 

If you are interested in this new professional challenge, we are looking forward to receiving your application. Please send your complete application documents in English or Greek to This email address is being protected from spambots. You need JavaScript enabled to view it.