Regional Clinical Scientist

hace 3 semanas


Madrid, Madrid, España Icon A tiempo completo
Job Title: Regional Clinical Scientist

At Icon, we are seeking a highly skilled and experienced Regional Clinical Scientist to join our team. As a key member of our clinical operations team, you will play a critical role in supporting the execution of clinical trials and ensuring the delivery of high-quality clinical data.

Key Responsibilities:

  • Provide scientific and clinical support to ongoing early and late-stage clinical trials, with a focus on protocol-specific, in-life clinical data monitoring activities.
  • Collaborate with cross-functional teams, including Clinical Development, Global Clinical Operations, Data Management, Biometrics, Patient Safety, Clinical Pharmacology, and Biomarkers, to support clinical study execution and clinical data monitoring.
  • Conduct daily medical surveillance of laboratory and ECG alerts, including review of eligibility criteria as appropriate.
  • Provide analytical support of clinical trial data, including assessment and follow-up of issues relating to protocol conduct and/or individual subject safety.
  • Generate study safety events trackers, periodic medical monitoring reports, and safety reviews in line with the needs of the study.
  • Participate in cross-functional study execution team activities relating to clinical data review.
  • Contribute to ICFs, training documents, and other clinical and regulatory documents under the direction of the Medical Monitor/Study Clinical Scientist as applicable.
  • Interact with internal and external stakeholders, including study sites, vendors, and other stakeholders, in support of clinical trial objectives related to subject safety and clinical data monitoring.

Requirements:

  • Life sciences degree (BS, MS, or Ph.D.) with clinical or pre-clinical research experience in the pharmaceutical industry or healthcare setting.
  • Experience in analysis and interpretation of clinical data, including safety and efficacy, and working knowledge of GCP and clinical trial execution.
  • Experience working with clinical trial sites and all stages of drug development.
  • Ability to make independent, timely, and appropriate decisions, and to handle multiple projects at a time with a strong attention to detail.
  • Excellent oral and written communication skills, and solid computer/analytical skills.
  • Ability to work collaboratively in a fast-paced, team-based matrix environment and to function independently as appropriate.
  • High level of organizational and project management skills.

About Icon:

Icon is a global provider of outsourced development and commercialization services to the pharmaceutical, biotechnology, and medical device industries. We offer a comprehensive range of services, including clinical development, regulatory affairs, and commercialization, to help our clients bring their products to market.

How to Apply:

If you are a motivated and experienced professional looking for a new challenge, please submit your application, including your resume and a cover letter, to [insert contact information].



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