Medical Pharmacologist (Scientific Writer)

ASPHALION; Almería; Híbrido; EUR 50.000 - 80.000; Jornada completa

Descripción de la vacante

ASPHALION, a growing company in the pharmaceutical industry, seeks a Medical Pharmacologist – Scientific / Clinical Expert to join their team. This role involves designing clinical development plans, managing client interactions, and writing regulatory documents. Ideal candidates will have advanced qualifications in Clinical Pharmacology, extensive clinical research experience, and a proactive attitude towards project management and regulatory compliance. Flexible work arrangements are available, allowing for home office or hybrid options.

Servicios

Permanent contract

Flexible work arrangements: Homeoffice, Hybrid, or Remote

Training and personal development programs

Formación

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

Responsabilidades

• Ensure timely and accurate execution of projects according to defined timelines.
• Design clinical development plans and create regulatory strategies.
• Write regulatory documents to support drug development.

Conocimientos

Proactive attitude

Good communication skills

Client-oriented approach

Advanced IT proficiency

Educación

Master's, 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:

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 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 (SA, PIP, ODD, IMPD, IB).
7. Interact directly with clients and multidisciplinary teams within the company to optimize projects and development programs.

Requirements:

• Master's, 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, client-oriented approach.
• Advanced proficiency in IT (MS Office).

We Offer:

• Permanent contract.
• Flexible work arrangements: Homeoffice, Hybrid, or Remote (located anywhere in Spain).
• A wide variety of projects, new challenges, and learning opportunities.
• Training and personal development programs.