Medical Pharmacologist (Scientific Writer)

ASPHALION; Palma de Mallorca; Híbrido; EUR 40.000 - 60.000; Jornada completa

Descripción de la vacante

Asphalion is seeking a Medical Pharmacologist to join their team in the pharmaceutical industry. This role involves ensuring project execution, designing clinical development plans, and managing regulatory submissions. The ideal candidate will have over 5 years of experience in clinical research and a Master’s or higher in Clinical Pharmacology. Flexible work arrangements are available, including options for remote work across Spain.

Servicios

Permanent contract

Flexible work arrangements

Training and personal development programs

Formación

• 5+ years of experience in clinical research.
• Experience in pharma or biotech sector.
• Proven experience in leading clinical development plans.

Responsabilidades

• Ensure timely project execution according to defined timelines.
• Design clinical development plans and regulatory strategies.
• Manage clients and partners, define milestones, and prepare project reports.

Conocimientos

Proactive attitude

Good communication skills

Client-oriented approach

Advanced IT proficiency

Educación

Master's degree, PhD, or Post-Doctoral qualification in Clinical Pharmacology

Herramientas

MS Office

Descripción del empleo

Asphalion is growing, and we are looking for a Medical Pharmacologist – Scientific / Clinical Expert to join our team of development, strategy, and scientific writing experts in the pharmaceutical industry! We seek someone who loves new challenges, enjoys working in an international environment, and wants to grow with us.

Main responsibilities:

• Ensure the timely and correct execution of projects according to defined timelines.
• Design clinical development plans.
• Develop regulatory strategies for First-in-Human Clinical trials and/or Marketing Authorization Applications (MAA).
• Manage clients and partners: define milestones, plan and execute tasks, manage timelines, and prepare project reports.
• Liaise with health authorities regarding drug development procedures and pre-submission meetings.
• Write regulatory documents to support drug development (e.g., SA, PIP, ODD, IMPD, IB).
• Maintain direct contact with clients and collaborate with multidisciplinary teams across the company to optimize projects and development programs.

Requirements:

• Master's degree, PhD, or Post-Doctoral qualification in Clinical Pharmacology.
• At least 5 years of experience in clinical research.
• Experience working in the pharma or biotech sector.
• Proven experience leading clinical development plans.
• Proactive attitude, good communication skills, and client-oriented approach.
• Advanced proficiency in IT (MS Office).

We Offer You:

• Permanent contract.
• Flexible work arrangements: home office, hybrid, or remote (location anywhere in Spain).
• Variety of projects, new challenges, and growth opportunities.
• Training and personal development programs.