Sr. Clinical Research Physician - Non-Obstructive Respiratory

Chiesi Farmaceutici S.p.A.; Parma; In loco; EUR 50.000 - 70.000; Tempo pieno

Descrizione del lavoro

A leading pharmaceutical company based in Parma, Italy, is seeking a Senior Clinical Research Physician to lead the design and execution of clinical studies in non-obstructive respiratory diseases. The ideal candidate will have at least 5 years of experience in the pharmaceutical industry, preferably in respiratory or allergy therapeutic areas, and a Medical Doctor Degree. This role involves collaborating with regulatory bodies and ensuring the integrity of clinical studies, with a focus on patient safety and data integrity.

Servizi

Flexible working approach

Remote working options

Tax assistance for foreign colleagues

Continuous training and development

Competenze

• At least 5 years in the pharmaceutical industry or equivalent expertise in clinical/academic research.
• Experience in therapeutic areas: Respiratory or Allergy & Immunology.
• Certification in Pulmonary or Allergy & Immunology is advantageous.

Mansioni

• Drive preparation of documents for regulatory submissions.
• Enhance clinical study execution and uphold medical integrity.
• Conduct review of clinical trial data ensuring data integrity and patient safety.
• Represent the company in front of regulatory agencies.
• Engage with external experts and regulatory bodies.

Conoscenze

Fluency in English

Excellent writing skills

Outstanding communication skills

Understanding of GCP and regulatory requirements

Ability to interpret complex data

Formazione

Medical Doctor Degree

Descrizione del lavoro

A leading pharmaceutical company based in Parma, Italy, is seeking a Senior Clinical Research Physician to lead the design and execution of clinical studies in non-obstructive respiratory diseases. The ideal candidate will have at least 5 years of experience in the pharmaceutical industry, preferably in respiratory or allergy therapeutic areas, and a Medical Doctor Degree. This role involves collaborating with regulatory bodies and ensuring the integrity of clinical studies, with a focus on patient safety and data integrity.