Medical Monitor (Oncology)

PSI CRO

Location: Italy
Work arrangement: Remote
Job type: Full-time
Pay: €80,000 – €119,000 / year
Posted today

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Key skills in this ad

Skills and tools

Clinical research
Google Cloud
Doctor

Languages

English

Picked out automatically from the employer's ad. Read the full description before applying.

About this role

PSI is seeking a Medical Monitor (Oncology) to join our international Medical Monitoring team.

In this role, you will provide medical oversight and expertise across global clinical trials, working closely with study sponsors, investigators, sites, project teams, and other clinical research professionals. Your contribution will help protect participant safety, maintain scientific and medical quality, and support the successful delivery of oncology studies.

This is an opportunity to apply your clinical oncology experience to international research and contribute directly to the development of new treatments for patients who need them.

Full-time employment

Responsibilities:

Serve as primary medical point of contact for clinical trial sponsors, internal project teams, investigators and trial sites for medical matters related to the conduct of clinical trials per protocol and per GCP guidelines

Provide medical oversight throughout the conduct of clinical trials, in accordance with the protocol, applicable regulations, and ICH-GCP requirements

Respond to medical questions from investigators, sites, sponsors, project teams, and third-party vendors

Provide medical input into eligibility assessments, protocol deviations, participant safety issues, and other trial-specific medical matters

Contribute medical expertise to clinical development plans, protocols, investigator brochures, informed consent documents, annual reports, clinical study reports, patient narratives, and scientific presentations

Review and assess clinical and safety data to support participant safety and identify medically relevant trends, risks, or quality concerns

Prepares and delivers medical training and/therapeutic area training to investigators and study teams

Support medical data review activities and contribute to the assessment of aggregated clinical trial data

Participate in bid defense meetings and proposal activities

Provide support with Pharmacovigilance activities

Identify medical trial risks, and collaborate with relevant functions to define appropriate mitigation and escalation measures

Support or participate in advisory boards, safety monitoring boards, and other medical or scientific committees, as applicable.

Help ensure that trial conduct and medical oversight activities comply with the approved protocol, applicable regulatory requirements, and quality standards

You will be a strong fit for this role if you have

Medical Doctor degree

Board certification in Oncology

Previous experience as a practicing Oncologist

Previous experience in clinical research or the pharmaceutical or CRO industry is a plus

Full professional proficiency in written and spoken English

Strong medical judgement, analytical thinking, and attention to detail

Clear communication and presentation skills, with the ability to explain complex medical information to different stakeholders

A collaborative and solution-oriented approach to working within international, cross-functional teams.

Proficiency in Microsoft Office applications and confidence working with clinical trial systems and digital collaboration tools.

The gross salary range for this role is 80,000 - 119,000 EUR and is determined based on qualifications and relevant professional experience.

As part of PSI's Medical Monitoring team, you will become part of an international team of medical professionals working at the frontline of clinical research. You will have the opportunity to apply your oncology expertise across global studies, collaborate with experienced colleagues, and contribute to bringing new treatment options to patients.

PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we undertake highlights our commitment to delivering high-quality, timely services across a broad spectrum of therapeutic indications.

At PSI, we foster an environment where a diverse range of colleagues feel welcomed and valued. Our inclusive culture is a cornerstone of our success, enabling us to attract and retain top talent globally.

We are not just about conducting clinical trials; we are about building a community where every team member has the opportunity to thrive and contribute to groundbreaking advancements in the pharmaceutical industry.

Originally posted on Himalayas

Pay

€80,000 – €119,000 / year

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