20 annunci per il ruolo di business development manager - lom (recruiting in corso)

Title Senior Manager Clinical Development Onco
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- Medicina
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IMI Plc - Legacy Precision —Levate, Lombardia
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Siemens Energy —Milano, Lombardia
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Nuvei —Milano, Lombardia
- 41.018 € - 57.900 € all'anno
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CHEP —Milano, Lombardia
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Senior Product Manager, Air Cooled Chillers & Heat Pumps, EMEA
Johnson Controls —Cinisello Balsamo, Lombardia
- 59.900 € - 89.900 € al mese
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Agile Lab —Milano, Lombardia
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Saint Gobain —Vimercate, Lombardia
- 50.000 € - 60.000 € all'anno
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Senior Product Manager
Haier Europe —Brugherio, Lombardia
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Lectra —Milano, Lombardia
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VERBUND AG —Milano, Lombardia
- 40.000 € - 50.000 € all'anno
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Dematic S.r.l. —Cernusco sul Naviglio, Lombardia
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Title Senior Manager Clinical Development Onco

Recordati -
Milano, Lombardia

Candidati adesso

Dettagli della posizione

Tempo pieno

Qualifiche

Medicina
Inglese
Google Cloud Platform
Microsoft Office

Descrizione completa della posizione

ID: 2569

Date of Posting: Jun 16, 2026

Business Area: Research & Development

Job Type: Direct Employee

On site / Remote / Hybrid: Hybrid

Hub Office: Milano, IT

Territory:

Full-Time or Part-Time: Full Time

Seniority: Mid-senior

At Recordati, we are united by a clear purpose: unlocking the full potential of life. With a century of history behind us, we are building the next chapter of our journey, continuing to grow while keeping patients at the centre of all we do.

What drives us is a shared belief that health, and the opportunity to live life to the full, should be within reach for everyone. This brings energy to our work, shaping how we support each other and show up every day. Our values – Better Together, Never Settle and Always Deliver – reflect this mindset, helping us to keep improving and make a meaningful difference.

Above all, these values bring to life our promise to everyone at Recordati, you can unlock your full potential. We know that people thrive when they can be themselves, are trusted and supported, and are given the opportunity to grow and make a meaningful contribution.

Are you ready to unlock your full potential?

Job Purpose

We are looking for a Senior Manager Clinical Development Onco to:

Provide comprehensive medical and scientific leadership to the design, set-up, execution and conduct of planned and ongoing clinical trials, from protocol development to study closure and Regulatory submission.
Support program and portfolio goals; may participate in the preparation of the Clinical Development Plans, based on the strategy agreed with the cross-functional Team.
Ensure that development strategies, trial designs, and execution plans are scientifically sound, operationally practical, and compliant with GCP standards and Regulatory expectations.
Act as clinical/medical contact for HAs, IRBs, ECs for any aspect related to the implementation and conduct of clinical trials.
Establish and maintain excellent partnership with the medical/scientific community and Key Opinion Leaders, as well as with Patient Associations.
Collaborate effectively with Clinical Pharmacology, Clinical Operations and Biostatistics to inform protocol design, amendments, and Regulatory interactions
Provide medical/clinical support to the Business Development Team

Key Responsibilities

Act as the medical expert to ensure that clinical trial designs, endpoints, and assessments are fit-for-purpose in rare disease settings, scientifically rigorous, and operationally feasible.
Lead the clinical components of key clinical trial documents, including clinical trial protocols and amendments, Investigator’s Brochures and updates, Informed Consent Forms, Medical Monitoring Plans, Safety Monitoring Plans, and statistical analysis plans.
Act as Medical Monitor to ensure continuous evaluation of clinical and safety data; provide medical support to investigators and CROs.
Maintain end-to-end medical oversight of trial execution in close partnership with internal functions and external stakeholders.
Ensure that the necessary regulatory, safety and data evaluation requirements are met in conjunction with the Regulatory and Pharmacovigilance Departments.
Act as primary contact for any study related medical/clinical questions and manage the preparation of responses to requests of Regulatory Authorities.
Provide scientific leadership during engagement with external experts and stakeholders, including investigators, key opinion leaders, advisory boards, and patient advocacy groups.
Contribute to Regulatory interactions, including preparation of clinical sections and participation to meetings as a medical expert.
May contribute to the preparation and the execution of clinical development plans in line with Company strategies and objectives.
Support Business Development and Licensing activities.
Maintain close relationship/provide clinical and medical support to Clinical Operation Team to ensure smooth and effective study setup and management.
Support Clinical Operations to identify high quality investigators and study sites for the conduct of clinical studies.
In cooperation with the Safety Leads, ensure that any important safety issues are discussed and handled with appropriate departments.
Work closely with Biostatistics/Data Management team to ensure Data Analysis and interpretation of data.
Collaborate with Clinical Pharmacology to interpret and contextualize pharmacokinetic and pharmacodynamic data.
Support preparation and finalistion of clinical study reports.
Support preparation of study related communication plans/ publications
Establish and maintain excellent professional relationships between the company and Key Opinion Leaders (KOL) and the broader medico-scientific community.
Support discussions related to potential investigator-initiated trials and relevance to Company portfolio and objectives.

Required Education

Medical Doctor Degree
Board Certification in Oncology/Haematology/Immunology will be considered a plus

Required Skills and Experience

At least 3 yrs clinical experience (trial experience desirable)
At least 5 yrs in the pharmaceutical/biotech industry
At least 3 yrs in a clinical development role, with direct medical monitor responsibility for clinical trials
Experience with Regulatory interactions and submissions
Experience within onco-haematology/immunology therapeutic areas and with rare diseases

Technical Competencies

Knowledge of clinical trial methodology, including trial set-up and conduct, protocol development, medical monitoring, review and interpretation of clinical data
Sound knowledge of GCP
Knowledge of Regulatory frameworks
Familiarity with fundamental clinical pharmacology and pharmacokinetic principles as applied to Oncology drug development (e.g., dose selection, exposure–safety relationships, and interpretation of PK outputs)
Ability to critically evaluate external assets and contribute to scientific and clinical due diligence for business development and portfolio expansion activities
Ability to interpret and communicate complex clinical and scientific data
Advanced communication skills with ability to interact with internal and external stakeholders
Ability to manage multiple tasks and respond to rapidly changing priorities

Required Behaviours and Competencies

Strong medical and scientific leadership, with the ability to influence and align diverse stakeholders
Strategic thinking combined with a hands‑on, accountable approach to program delivery
High level of scientific integrity, decision‑making rigour, and attention to detail
Collaborative mindset with the ability to operate effectively in a global matrix organization

Required Languages

Fluency in spoken and written English

At Recordati we believe in people! Inspired by our purpose - unlocking the full potential of life - we are committed to creating a diverse environment and cultivating a culture of inclusion. We strive to continually lead with our values and beliefs, enabling our employees to bring their whole selves to work and develop their potential.

We are proud to be an equal opportunity employer. We recruit, develop and reward without regard to, amongst others, gender, sexual orientation, gender identity or expression, national origin, age, physical or mental ability, race, ethnicity, political or religious belief.

If you are looking to join a company where you can try new things, speak openly, and be bold, we invite you to apply today.

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