Medical Oncologist Manager - Early Clinical Development

buscojobs España; Ourense; Presencial; EUR 70.000 - 90.000; Jornada completa

Descripción de la vacante

A leading company in marine-derived medicines is seeking a Medical Oncologist Manager for Early Clinical Development. The role involves medical oversight of clinical programs, strategic contributions, and ensuring compliance with regulations. Candidates should have a Medical Degree and experience in oncology clinical trials. The position offers a permanent contract with flexible hours and health insurance.

Servicios

Permanent full-time contract with flexible start times

Shorter working hours on Fridays

Stock plan

Private health insurance

Formación

• Minimum 3 years of experience in clinical research and/or oncology drug development.
• Fluency in English with the ability to communicate complex medical information.

Responsabilidades

• Medical oversight and monitoring of early-stage clinical development programs.
• Lead the design and implementation of clinical studies, ensuring regulatory compliance.
• Act as Medical Monitor, resolving critical clinical issues.

Conocimientos

Oncology

Clinical Research

Communication

Clinical Trial Design

Educación

Medical Degree (MD)

Descripción del empleo

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Job Reference :

791985362434208563232460

Job Views : Posted :

31.03.2025

Expiry Date : 15.05.2025

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Job Description :

At Claire Joster , we are collaborating with PharmaMar , a global leader in the research and development of innovative marine-derived medicines for oncology. We are currently seeking a Medical Oncologist Manager, Early Clinical Development to join their team.

Mission of the Role :

Medical oversight and monitoring of early-stage clinical development programs in oncology for PharmaMar’s emerging pipeline compounds.

Key Responsibilities :

Expertise & Strategic Contribution :

• Serve as an internal clinical expert in translational and clinical oncology , providing scientific and medical support for ongoing projects.
• Contribute strategically to clinical study decision-making (from Phase I to Phase IIa ).

Study Phases :

1.Study Design & Initiation :

• Lead the design and implementation of clinical studies , ensuring regulatory compliance.
• Develop protocols, eligibility criteria, safety monitoring procedures, and risk mitigation strategies .
• Collaborate with internal teams and CROs for study planning.
• Train investigators and study personnel .

2.Study Execution :

• Act as Medical Monitor , resolving critical clinical issues.
• Oversee study integrity , including safety and efficacy data interpretation .
• Monitor patient enrollment and adherence to study timelines.
• Assess and report serious adverse events (SAEs) .
• Contribute to Development Safety Update Reports (DSURs) .

3.Study Closure :

• Analyze and interpret clinical data.
• Draft key sections of Clinical Study Reports (CSR) .

4.Ongoing Responsibilities :

• Supervise Clinical Scientists working on related programs.
• Engage with Key Opinion Leaders (KOLs) in the field.
• Ensure compliance with international regulatory requirements and participate in key regulatory discussions.
• Maintain adherence to Good Clinical Practices (GCP) and pharmacovigilance regulations .

Requirements :

• Medical Degree (MD) with a scientific background in Oncology .
• Experience in early-phase clinical trials ( FIH, Phase I / II ).
• Advanced knowledge and experience in clinical trial design, safety, trial management, and clinical data management .
• Strong understanding of clinical trial regulations and Good Clinical Practices (GCP) .
• Knowledge of pharmacokinetics and pharmacodynamics and their role in clinical development strategy.
• Proven ability to integrate preclinical and clinical data into decision-making.
• Fluency in English with the ability to communicate complex medical information clearly and effectively, both verbally and in writing.
• Minimum 3 years of experience in clinical research and / or oncology drug development in the pharmaceutical, academic, or CRO environment.
• International experience is a plus.

What We Offer :

• Permanent full-time contract with flexible start times
• Shorter working hours on Fridays
• Stock plan
• Private health insurance

PharmaMar is committed to promoting equal opportunities for all individuals, regardless of race, sex, gender, religion, or sexual orientation. We actively work to eliminate barriers to discrimination and foster a diverse and inclusive work environment

Se ofrece : J-18808-Ljbffr