Medical Pharmacologist (Scientific Writer)

buscojobs España; Palencia; Presencial; EUR 50.000 - 70.000; Jornada completa

Descripción de la vacante

A leading pharmaceutical company is seeking a Medical Pharmacologist – Scientific / Clinical Expert to manage diverse clinical projects and regulatory strategies. Candidates should possess a Masters or higher in Clinical Pharmacology with at least 5 years of clinical research experience. The role offers flexibility with options for remote work and a commitment to professional development.

Servicios

Permanent contract

Flexible working options

Training and personal development programs

Well-being programs

Dynamic work environment

Inclusive and high-performance culture

Formación

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

Responsabilidades

• Ensure timely execution of projects based on defined timelines.
• Design clinical development plans and regulatory strategies.
• Manage clients and partners to optimize drug development.

Conocimientos

Communication

Client-oriented mindset

Proactivity

IT proficiency

Educación

Masters in Clinical Pharmacology

PhD in Clinical Pharmacology

Post-Doctoral degree 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:

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

Requirements:

1. Masters, PhD, or Post-Doctoral degree in Clinical Pharmacology.
2. At least 5 years of experience in clinical research.
3. Experience working in the pharma or biotech sector.
4. Proven experience leading clinical development plans.
5. Proactive attitude, strong communication skills, and client-oriented mindset.
6. Advanced proficiency in IT (MS Office).

We Offer:

• Permanent contract.
• Flexible working options: Homeoffice, Hybrid, or Remote (location anywhere in Spain).
• A wide variety of projects, new challenges, and opportunities for growth.
• Training and personal development programs.
• 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 more than 15 nationalities.
• Well-being programs focusing on physical, psychological, and emotional health.
• Internal activities and CSR initiatives.
• Equal Opportunity Employer.