Medical Advisor

Philogen S.p.A.; Siena; In loco; EUR 90.000 - 130.000; Tempo pieno

Descrizione del lavoro

A leading biotech company in Italy is seeking a highly motivated Medical Advisor to support the management of clinical trials in oncology and rheumatology. The ideal candidate will contribute to trial design, execution, and analysis, and must possess excellent English skills along with the ability to work independently. This position offers a contract and salary based on experience, and welcomes applications from diverse candidates.

Competenze

• Must have excellent English skills, both written and spoken.
• Good interpersonal skills are essential.
• Ability to build trust and confidence in teams and departments required.
• Must be able to work independently.

Mansioni

• Contribute to the design, execution, and analysis of clinical trials.
• Provide expert guidance and support in designing clinical trials.
• Support monitoring efficacy and safety trends by reviewing data.
• Interact with clinical site staff to advance clinical trials.
• Contribute to dissemination of scientific knowledge through publications.
• Contribute to publication and conference dissemination of scientific knowledge.
• Work closely with cross-functional teams (PMs, PV, Regulatory, Clinical Ops).
• Act as a role model for stakeholders in leading trials and supporting the Company’s strategy.
• Interact with regulatory authorities to support development programs.

Conoscenze

Excellent level of English

Good interpersonal skills

Ability to work independently

Ability to build trust and confidence

Descrizione del lavoro

Philogen S.p.A., a biotech company listed on the Milan Stock Exchange and a leader in the development of innovative anti-tumor therapies, is looking for a highly motivated and qualified MEDICAL ADVISOR. The successful candidate will have the responsibility for supporting the management and development of Philogen’s clinical trials in oncology and rheumatology and will report to the Chief Medical Officer.

In particular the successful candidate will be responsible for:

• Contributing to the design, execution and analysis of clinical trials:
• providing expert guidance and support in designing and writing clinical trials
• providing support in monitoring efficacy and safety trends by reviewing clinical data and feeding up the analysis data set
• providing support in reviewing regulatory and pharmacovigilance documentations
• interacting with Principals Investigators and clinical site staff to advance the performance of clinical trials
• contributing to the dissemination of scientific knowledge through publications and conferences
• Working closely with the cross-functional team (Project Managers, Pharmacovigilance, Regulatory Affairs and Clinical Operation)
• Acting as a role model for the internal and external stakeholders in leading clinical trials and supporting the Company’s strategy
• Interacting with regulatory authorities to support the Company’s development programs

The ideal candidate should have:

• An excellent level of English, both written and spoken
• Good interpersonal skills
• Ability to build trust and confidence in teams/departments
• Ability to work independently

We offer:

A contract and salary proportional to the experience of the successful candidate.

Job location:

We invite interested candidates to submit their applications expressly authorizing the processing of personal data in accordance with Legislative Decree 196/2003. Our recruitment adheres to the provisions of Legislative Decree 198/2006, and we welcome applications from candidates of any gender orientation or expression, sexual orientation, age, ethnicity, or religious belief.