Senior Clinical Research Physician Non-Obstructive Respiratory Diseases

Chiesi Group; Parma; Ibrido; EUR 70.000 - 90.000; Tempo pieno

Descrizione del lavoro

A leading pharmaceutical company in Parma is looking for a Senior Clinical Research Physician to provide scientific and strategic leadership in clinical studies related to non-obstructive respiratory diseases. The ideal candidate will have at least 5 years of experience in the pharmaceutical industry, with a strong background in clinical or academic research. We offer a flexible working approach, remote working opportunities, and various employee support services.

Servizi

Continuous training and development

Support in relocation process

Tax assistance service

Flexible working approach

People-care services

Competenze

• At least 5 years in the pharmaceutical industry preferred, or equivalent expertise.
• Experience in Interstitial Lung Disease or Pulmonary Hypertension is a plus.
• Fluency in spoken and written English is required.

Mansioni

• Drive medical input into clinical trial design.
• Conduct ongoing medical review of clinical trial data.
• Ensure compliance with regulatory requirements.
• Represent the company in discussions with health authorities.
• Collaborate with various functions for clinical development plans.

Conoscenze

Excellent writing skills

Outstanding communication skills

Strong understanding of GCP

Ability to interpret clinical data

Formazione

Medical Doctor Degree

Certification in Pulmonary or Allergy & Immunology

Descrizione del lavoro

Who we are looking for

Purpose

The Senior Clinical Research Physician provides scientific and strategic leadership in the design, execution, and interpretation of global clinical studies in the non-obstructive respiratory diseases therapeutic area.

They will drive the preparation of documents for regulatory submissions, ensuring the scientific validity and rigor of key documents, including study protocols, investigator brochures, and clinical study reports.

They are able to work comfortably in a matrix environment and is an integral member of the cross-functional clinical study team. They use therapeutic expertise to ensure incorporation of robust scientific principles into study design and conduct and to enhance competencies across R&D.

Main Responsibilities

• Enhances clinical study execution, working cross-functionally with internal stakeholders and the Clinical team to uphold medical and scientific integrity across clinical trials.
• Drive medical and scientific input into clinical trial design and execution in accordance with the Clinical Development Plan and related key clinical documentation (e.g. clinical section of the Investigator’s Brochure, Protocols and Clinical Study Reports).
• Conduct ongoing medical and scientific review of clinical trial data, ensuring data integrity, patient safety and the ongoing benefit-risk assessment
• Responsible for the clinical interpretation of study data and communication to internal and external stakeholders
• Ensure the safeguard of Patients Safety : in collaboration with and in support of Corporate Pharmacovigilance identify safety signals, review narratives, take actions with investigators when Serious / unexpected Adverse Events are reported
• Represents the company in front of health authorities, regulatory agencies, external partners, and scientific institutions, contributing to regulatory discussions and ensuring alignment with Global Clinical Development objectives.
• Collaborate with Clinical Program Leaders, statisticians, regulatory affairs, and other key functions to drive clinical development plans and contributes to regulatory submission documentation
• Engage with external experts, regulatory bodies, ethics committees, investigators, and safety monitoring committees to ensure alignment with scientific and medical needs.
• Be delegated to replace CPL or be assigned as CPL for some specific phase of the clinical programs
• Provide medical and scientific inputs in RWE studies / disease registries

Experience Required

At least 5 years in the pharmaceutical industry preferred although equivalent expertise in clinical or academic research will be considered, preferably within the Respiratory or Allergy & Immunology therapeutic areas.

Experience within the specific therapeutic area (Interstitial Lung Disease; Pulmonary Hypertension) and experience in pharmaceutical / biotech industry are preferred and will be a plus.

Education

Medical Doctor Degree from a recognised institution; certification in Pulmonary or Allergy & Immunology considered an advantage.

Languages

Fluency in spoken and written English

Technical Skills

• Excellent writing skills in order to effectively contribute to study documentation and reports.
• Outstanding communication skills with ability to interact with all internal stakeholders and external academic and regulatory experts.
• Strong understanding of GCP, regulatory requirements, and clinical trial methodologies.
• Ability to interpret and effectively communicate complex clinical and scientific data, and literature.

What we offer

You would join a dynamic, fast-growing, challenging and friendly environment.

In Chiesi we firmly believe that our people are our most valuable asset , that is why we invest in continuous training, learning and development. Therefore, we strive to continuously promote and satisfy development needs, paying particular attention to the quality of our working environment and to collective well-being.

We want our people to come to work happy every day , and we know how important it is to find the right work-life balance in order to be able to give our best. That is why we offer flexible working approach, remote working, support in the relocation process, tax assistance service for foreign colleagues and many other people-care services.