Medical Pharmacologist (Scientific Writer)

ASPHALION; Murcia; Híbrido; EUR 45.000 - 70.000; Jornada completa

Descripción de la vacante

Join a leading company in the pharmaceutical industry as a Medical Pharmacologist – Scientific / Clinical Expert. You will ensure timely project execution and develop clinical plans while managing relationships with clients and health authorities. This role offers a permanent contract, flexible working options, and growth opportunities in a dynamic environment.

Servicios

Permanent contract with flexible working schedule

Home office, hybrid, or remote model

Training and personal development programs

Well-being programs for health

Formación

• Medicine Degree or relevant higher qualification is mandatory.
• 5+ years of experience in clinical research.
• Experience in the pharma or biotech sector.

Responsabilidades

• Design and execute clinical plans and regulatory strategies.
• Manage client relationships and project timelines.
• Write regulatory and clinical documents.

Conocimientos

Project management

Communication

Client orientation

Proactive attitude

IT skills (MS Office)

Educación

Medicine Degree

Clinical Pharmacology Masters

PhD or 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 include:

1. Ensuring the timely and accurate execution of projects according to defined timelines.
2. Designing clinical plans and creating regulatory strategies for First-in-Human Clinical Trials and/or MAA.
3. Managing client and partner relationships: defining milestones, planning and executing tasks, managing timelines, and reporting on projects.
4. Liaising with health authorities regarding drug development procedures and pre-submission meetings.
5. Writing regulatory documents to support drug development (e.g., SA, PIP, ODD, IMPD, IB).
6. Writing clinical documents and maintaining direct contact with clients and multidisciplinary teams across the company to optimize projects and development programs.

Requirements:

• Medicine Degree, Clinical Pharmacology Masters, PhD, or Post-Doctoral qualification.
• At least 5 years of experience in clinical research.
• Working experience in the pharma or biotech sector.
• Project management skills and experience leading clinical development plans.
• Proactive attitude, good communication skills, and client orientation.
• Fluent in English and Spanish.
• Advanced IT skills (MS Office).

We Offer You:

• Permanent contract with flexible working schedule (Friday until 15:30), home office, hybrid, or remote model.
• Location anywhere in Spain.
• Variety of projects, new challenges, and growth opportunities.
• 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 Companionship.
• A dynamic working environment with employees from over 15 nationalities.
• Well-being programs covering physical, psychological, and emotional health.
• Internal activities and RSC initiatives.

Our commitment: We are an Equal Opportunity Employer.