Clinical Research Physician/Investigator

Category: Clinical Development

Location:Gentofte, Capital Region of Denmark, DK

• Ensuring the safety, well-being, and rights of clinical trial participants.
• Contributing to the daily operation, planning, and management of clinical activities at CLINi C.
• Developing trial protocols and leading trial teams.
• Setting and maintaining training standards for CLINi C staff, with a focus on clinical trial processes and managing medical emergencies.
• Responsible for clinical oversight and governance, including management of protocol deviations, trial risk assessments, site risk assessments, CAPAs, and issue management.
• Delivering accurate scientific and medical input to stakeholders, interpreting and communicating scientific data and assessing the impact of new findings.

• A specialization and excellent clinical experience in either Internal Medicine, or Anesthesiology, including competencies in Emergency Medicine, assessing ECG and laboratory results, along with knowledge of the Danish healthcare system. In addition to being fluent in English, proficiency in Danish is also required in this case. Knowledge in Clinical Pharmacology is highly appreciated.
• Or with vast hands-on experience as an investigator in conducting early phase trials, in e.g. First-in-Human (FIH) trials and experienced in Clinical Pharmacology. For this role, there is no need to be able to speak Danish or have knowledge of the Danish healthcare system.

• Are a Medical Doctor with documented clinical and scientific merits from a Ph D degree or equivalent.
• Either bring proven clinical experience in either Internal Medicine or Anesthesiology/ Emergency Medicine
• Or have demonstrated expertise in overseeing early clinical trials as an investigator, with a strong foundation in clinical trial methodology and adherence to all relevant regulations, including GCP-ICH standards.

• Proven experience in teaching and guiding clinical or trial staff, enhancing team skills, and promoting compliance with clinical best practices.
• Knowledge in Clinical Pharmacology.
• Experience with strategic and scientific planning in clinical development within the pharmaceutical industry, along with a strong understanding of the pharmaceutical business, is preferable.