Position Associate Medical Director
Department Clinical Development, Medical - Oncology
Responsible To Chief Medical Officer
Location Prague, Czech Republic
Employment Type Full Time Employment

Key Activities and Responsibilities

General Objectives:

  • Assists in execution of the Clinical Development Plan (CDP) for the compound within the selected indication(s).
  • Assist in efficient and safe development of the compound in indication(s) assigned, including competent medical monitoring of individual clinical trials.
  • Medical representation of the company to the outside world in relation to the assigned compound and indication(s).

Major Tasks:

  • Medical monitoring of trials, with focus on medical review of study documentation and individual patient information, investigator communication, and continuous safety evaluation (in cooperation with pharmacovigilance department).
  • Author, and/or support writing, and/or reviewing of medical documents; such as clinical study protocols, investigator's brochures, clinical study reports, clinical development plans, manuscripts for publication of research results, literature reviews, internal and external presentations, newsletters, sections of INDs/CTAs, other regulatory documents.
  • Support development of case report forms, statistical analysis plans (including study report tables and listings), and other related documents (e.g., automated query definitions) together with data management and statistics.
  • Close interaction across the whole development team (medical + operational + regulatory + safety + data management/statistics + medical affairs etc.; both locally and internationally) to support efficient and safe conduct of clinical studies.
  • Support of due-diligence processes when applicable.
  • Establish and maintain close interaction with opinion leaders within the appropriate area of work (compound in selected indication(s)) to secure support for the clinical program.
  • Oncology medical training and education of other employees when appropriate.
  • To participate at preparation of Advisory Boards and Investigator’s Meetings.

Competences, Skills and Qualification


  • MD with oncology or hematology specialization (one can also consider other MD specialization, but then longer industry experience in oncology/hematology is a pre-requisite).

Professional Experience:

  • Sufficient drug development industry experience, i.e. at least 2-3 years. If an adequate time has been spent on drug development in academia, e.g. university or cooperative group setting, this could compensate for a shorter experience within the drug development industry.
  • Experience in clinical study responsibility (i.e. as medical monitor of studies).
  • Adequate knowledge of ethical principles and drug laws and regulations to be able to function as medical monitor of clinical studies.
  • Experience in medical review of important (preferentially pivotal) clinical studies.
  • Experience in early and /or late stage clinical development is preferred
  • Experience in the basic medical bio-statistic and interpretation of clinical trial results.
  • Experience in the field of pharmacovigilance incl. national and EU legislative knowledge.
  • International experience desirable.

Other Skills (language, IT):

  • English, excellent verbal fluency and written proficiency is a must.
  • Good knowledge of MS-Office.

Personal Skills:

  • Dynamic, team- and goal-oriented, personality.
  • Very good communication and presentation skills.
  • Highest integrity regarding data assessments as well as interaction in team and company settings.
  • Preferentially shown ability to work in global setting.
  • Good time management.
  • Willingness to travel.

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