Medical Pharmacologist (Scientific Writer)

ASPHALION; Santander; A distancia; EUR 50.000 - 80.000; Jornada completa

Descripción de la vacante

ASPHALION is seeking a Medical Pharmacologist – Scientific / Clinical Expert to oversee project execution, manage client relationships, and design clinical plans. This role requires a Medicine Degree and over 5 years of clinical research experience. The position offers a flexible contract with options for hybrid or remote work, highlighting a commitment to personal development and well-being in the workplace.

Servicios

Flexible working schedule

Home office and hybrid work options

Training and personal development programs

Well-being programs

Dynamic working environment

Formación

• 5+ years of experience in clinical research.
• Relevant working experience in pharma or biotech sectors.
• Proactive attitude and skills in managing timelines.

Responsabilidades

• Ensure timely execution of projects according to defined timelines.
• Design clinical plans for First-in-Human Clinical Trials.
• Liaise with health authorities for drug development procedures.

Conocimientos

Project Management

Excellent Communication

Client Orientation

Fluency in English

Fluency in Spanish

Advanced IT Skills

Educación

Medicine Degree

Clinical Pharmacology Master’s

PhD

Post-Doctoral Qualification

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:

1. Ensure the timely and correct execution of projects according to defined timelines.
2. Design clinical plans and create regulatory strategies for First-in-Human Clinical Trials and/or MAA submissions.
3. Manage client and partner relationships: define milestones, plan and execute tasks, manage timelines, and report on projects.
4. Liaise with health authorities for drug development procedures and pre-submission meetings.
5. Write regulatory documents to support drug development (e.g., SA, PIP, ODD, IMPD, IB).
6. Write clinical documents and maintain direct contact with clients and multidisciplinary teams to optimize projects and development programs.

Requirements: A Medicine Degree, Clinical Pharmacology Master’s, PhD, or Post-Doctoral qualification; +5 years of experience in clinical research; relevant working experience in pharma or biotech sectors; project management skills; experience leading clinical development plans; proactive attitude; excellent communication skills; client-oriented mindset; fluent in English & Spanish; advanced IT skills (MS Office).

We Offer You:

• Permanent contract with flexible working schedule (Friday until 15:30), home office, hybrid, or remote work options.
• Location: Anywhere in Spain.
• Variety of projects, new challenges, and opportunities for growth.
• Training and personal development programs, including English lessons.
• A professional, inclusive, and high-performance work environment to develop your skills and advance your career.
• A company culture built around Passion, Flexibility, Commitment, Quality, and Camaraderie.
• A dynamic working environment with employees from over 15 nationalities.
• Well-being programs focusing on physical, psychological, and emotional health.
• Internal activities and corporate social responsibility initiatives.
• Equal Opportunity Employer.