Medical Director, Medical Affairs

This is a fully remote position, open to applicants in Spain, +2 more countries.

📋 Description

• Assist the leadership of the Medical Affairs department in crafting and executing medical and operational strategies, policies, and procedures.

• Oversee and engage in medically related activities throughout the planning and execution of clinical trials.

• Support the study feasibility process and be actively involved in all matters concerning patient safety and pharmacovigilance, medical monitoring, medical training, and business development.

• Provide daily leadership and manage team members within the Medical Affairs Department.

• Responsible for multiple projects and clients, ensuring effective management of client relationships and business expectations while delivering successful outcomes.

• Foster a proactive, positive, and results-driven work environment.

⛳️ Requirements

• A post-graduate degree in a medical or health-related field is required (MD, BOARD CERTIFICATION IS A PLUS).

• A minimum of 10 years of relevant medical work experience is required; previous experience in a clinical research setting is strongly preferred.

• At least 5 years of experience in people management or leading project teams is required.

• Proficiency in International Conference on Harmonization (ICH) Good Clinical Practice (GCP) guidelines and other applicable regulatory rules and guidelines, along with a strong understanding of medical terminology, clinical trials, and clinical research is required.

• Proven ability to effectively solve problems, demonstrate sound judgment, lead by example, and influence without direct authority is required.

• Capacity to think strategically and leverage expertise to act as a consultant and business partner for both internal and external clients is required.

• Exceptional written and verbal communication skills, including technical writing proficiency and familiarity with moderately complex study designs and regulatory requirements applicable to Phase I-IV clinical trials, are required.

• Knowledge of the relationship and regulatory obligations between the contract research organization (CRO) industry and pharmaceutical/biotech companies is required.

• Demonstrated ability to lead by example and exhibit technical and supervisory leadership skills is required.

• Proficient in computer software applications, including Microsoft Word and Microsoft Excel, with the aptitude to learn new software is required.

• Ability to establish and maintain trust and confidence while communicating effectively with clients, external vendors, and internal team members is required.

• Capability to mentor others and effectively delegate tasks is required.

🏝️ Benefits

• A flexible and inclusive culture with a workforce that is 70% remote.

• Teams that are 66% women-led.