Medical Affairs

Job ResponsibilitiesProject management of clinical studies sponsored by Bluepharma;Oversight of clinical, bioanalytical and monitoring activities of clinical studies sponsored by Bluepharma;Prepare monitoring plans and perform monitoring visits to clinical and bioanalytical sites (CRA role);Evaluate and prepare clinical development plans for new business opportunities (generic and value added products);Support activities related to clinical studies sponsored by third-parties.Minimum RequirementsBachelor's Degree in Life or Pharmaceutical Sciences and/or relevant work experience (previous experience in similar or related jobs is preferred);Strong knowledge of Good Clinical Practice/ICH guidelines and other applicable regulatory requirements is preferred;Fluency in written and spoken English;Proficiency in Microsoft Office applications - Word, Excel, PowerPoint and Outlook – is preferred;Strong organizational and problem-solving skills;Attention to detail, curious and proactive profile;Excellent communication, presentation, and interpersonal skills;Fast learning ability and adaptability in fast-paced working environment;Ability to manage time and work independently;Capacity to deal with tight deadlines;Flexibility to travel on a regular basis.
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