Sr. Clinical Research Associate

TN Italy; Milano; Ibrido; EUR 40.000 - 70.000; Tempo pieno

Descrizione del lavoro

A leading company in the biopharmaceutical sector is seeking a Senior Clinical Research Associate to join their dynamic team. This role involves independently managing clinical trial monitoring, ensuring compliance, and mentoring junior staff. The ideal candidate will have significant experience in complex trials, particularly in oncology or rare diseases, and possess strong communication skills in both English and Italian.

Servizi

Competitive salaries and comprehensive benefits package

Departmental Study/Training for professional development

Internal growth opportunities

Financially rewarding internal employee referral program

Employee recognition programs

Loyalty Award Program

Competenze

• 3+ years experience as a Certified CRA.
• Strong understanding of ICH-GCP and regulatory guidelines.
• Fluent in English and Italian.

Mansioni

• Manage all aspects of monitoring for assigned clinical trials.
• Ensure compliance with protocols and regulatory requirements.
• Mentor and support junior CRAs.

Conoscenze

Communication

Leadership

Problem Solving

Formazione

Certified CRA according to Italian DM 15 Nov 2011

Descrizione del lavoro

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Bring your monitoring expertise to the forefront of innovation

We are looking for a Sr. Clinical Research Associate (Sr. CRA) to join our A-team (hybrid). As a Sr. CRA at Allucent, you will independently control and monitor investigational sites, pro-actively detect issues, provide solutions to ensure clinical studies are performed according to the trial protocol and in compliance with SOPs, applicable regulations, and the principles of Good Clinical Practice.

At Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe. We know all our colleagues by name and work together as a team to make everyone SHINE.

The role

As a Senior CRA, you will take the lead on monitoring activities, owning your sites and relationships with investigators. You’ll be the bridge between sponsor and site, ensuring trial integrity while being supported by a collaborative, experienced team. You will be a mentor for junior team members and contribute to grow our success. You will travel throughout Italy.

Main responsibilities:

• Independently manage all aspects of monitoring for assigned clinical trials across study phases, including site initiation, routine monitoring, and close-out visits.
• Ensure compliance with protocols, GCP, ICH, SOPs, and applicable regulatory requirements.
• Build strong site relationships, acting as a primary point of contact and ensuring high-quality data collection.
• Identify and resolve site issues, escalating as needed to maintain trial integrity and patient safety.
• Mentor and support junior CRAs, sharing knowledge and best practices.

Requirements

Who are we looking for:

You’re an experienced CRA / monitor ready to take the next step with a company that truly values your expertise and independence. You thrive in an agile, collaborative environment and want to be part of a team making a real impact.

• Experience leading monitoring activities in complex trials, ideally in oncology or rare disease with a minimum of at least 3 years’ experience as Certified CRA according to Italian DM 15 Nov 2011
• Strong understanding of ICH-GCP and regulatory guidelines.
• Clear and confident communicator in English and Italian.
• Comfortable working independently and managing priorities.
• Willingness to travel in Italy, as required.

Benefits of working at Allucent include:

• Competitive salaries and a comprehensive benefits package
• Departmental Study/Training for furthering professional development
• Internal growth opportunities and career progression
• Financially rewarding internal employee referral program
• Eligibility for our internal employee recognition programs for going above and beyond on projects
• Eligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employees

About Allucent

Our mission is to help bring new therapies to light. When you work at Allucent, that means applying your unique skill set, expertise, and knowledge to build partnerships with our clients in their pursuit to develop new, life-improving treatments.

If you're passionate about helping customers develop new pharmaceuticals and biologics; have an entrepreneurial spirit; and ready to join other science, business, and operations leaders, we would love to get to learn more about how we can help each other grow.

Together we . Find more information about our values.

Apply now!

If you are interested in this role please apply through the button or for more information reach out to Yael Kokernoot,

Disclaimers:

*Our hybrid work policy encourages a dynamic work environment, prescribing 2 days in office per week for employees within reasonable distance from one of our .

“The Allucent Talent Acquisition team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively “Allucent”). Allucent does not accept unsolicited resumes from third-party recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third-party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources.”