Experienced Clinical Research Physician (based in Netherlands)
Nr ref.: /JOBS.pl
In this position you play an important role in the implementation of drug development programs for novel and existing compounds. You will work closely with drug development project teams to ensure successful execution of protocols.
You will play a key role in the design, conduct, analysis, and reporting of phase I-III clinical trials including protocol development, evaluation of safety information, data analysis and interpretation, and report writing. You may participate in one or more study teams and may have oversight of multiple study protocols. Your presence at the Dutch office for a minimum of 3 days a week is required.
Duties & Responsibilities The Clinical Research Physician
Provides medical/scientific input to clinical protocols and to study objectives, to selection of study populations, variables and selection of appropriate testing to monitor the safety of subjects during the study Is primarily responsible for medical and safety monitoring by detailed review of single patient data of enrolled subjects in Phase I-III studies. Participates in interpretation and assessment of trial data and supports the writing of clinical study reports. Supports medical sciences in regulatory interactions and negotiations. Stays abreast of internal and external developments (scientific, clinical, commercial, competitive, legal, and regulatory). This includes review of published scientific medical literature relevant for the execution of the clinical study protocols. Develops or maintains knowledge of therapeutic area specialty to ensure protocol is appropriately designed and executed from a medical/scientific perspective.
Competences Affinity with scientific data, experience with systems and applications that are generally used in medical science, quick and independent learner, team player, excellent communication skills, leadership skills, able to manage complex medical and clinical issues and data, able to manage multiple projects at the same time.
Registered and licensed MD or equivalent. 1-3 years hospital experience as treating Physician At least 2-3 years of experience in drug development at a biotech or pharmaceutical company as Study Physician or Medical Monitor in Clinical R&D Good working knowledge of regulatory procedures and Good Clinical Practice guidelines. Able to work effectively across different functions and cultures Experience in Urology and / or Nephrology is preferred.