Clinical Research Associate II / Senior Clinical Research Associate

Precision For Medicine; Torino; In loco; EUR 40.000 - 60.000; Tempo pieno

Descrizione del lavoro

A clinical research organization is looking for a Clinical Research Associate (CRA) to monitor clinical studies in Torino, Italy. The ideal candidate will have a 4-year college degree, CRA certification, and at least 4 years of experience in the CRO or pharmaceutical industry, preferably with oncology experience. Responsibilities include coordinating study activities and mentoring junior staff, with travel commitment of 50-60%.

Competenze

• 4+ years of experience in the CRO or pharmaceutical industry.
• Oncology experience preferred.
• Fluency in English and local language required.

Mansioni

• Monitor and own the progress of clinical studies.
• Coordinate activities required to set up and monitor studies.
• Train and mentor junior staff.

Conoscenze

Attention to detail

Conflict resolution

Creativity in problem solving

Formazione

Bachelor's degree or equivalent

CRA certificate

Descrizione del lavoro

About You

You are calm, thoughtful, and responsive when things don’t go as planned.

You are well-prepared, whether it be for an investigator meeting, site visit or project team update, always staying two steps ahead of the game.

You find quick and creative ways of overcoming difficulties.

You have an impeccable eye for detail.

You identify potential study risks and propose solutions on how to mitigate them.

You take responsibility in the quality and outcomes of your work.

You are adept at handling conflict by using tried and true resolution strategies.

How We Will Keep You Busy and Support Your Growth

You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH‑GCP, and all applicable regulations and standards.

You will coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre‑study and initiation visits, etc.).

Senior CRAs handle appropriately sized clinical trials, and support Project Managers with trials that are larger in scope.

You will also have the opportunity to train and mentor junior staff members.

You will interact directly with clients, initiate payments, and participate in proposal activities, including development and client presentations.

Qualifications

Minimum Required:

• 4-year college degree or equivalent experience
• Holder of CRA certificate

Other Required

• CRA experience within the CRO or pharmaceutical industry; 2+ years for a CRA II and 3+ years for Senior CRAs
• Oncology experience
• Availability for domestic travel including overnight stays, which may constitute up to approximately 50‑60% travel commitment (international travel may be required for some senior level positions)
• Fluency in English and for non‑English speaking countries the local language of country where position based

Preferred

• Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline
• Two+ years of oncology experience
• Study start up activities experience
• For Senior CRAs, understanding of financial management

Please, apply in English.

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