MEDICAL DIRECTOR - NEUROLOGY

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We are looking to recruit an experienced Neurologist with a passion for clinical research to join an international Clinical Research Organization (CRO). This role is ideal for an MD who thrives in dynamic and innovative environments, where their medical expertise can drive cutting-edge treatments in development. If this describes you, we invite you to explore this opportunity.

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This role can be located in a variety of European countries (EU, plus UK and Serbia). This is a full-time, permanent contract role, that can be fully remote (home-based) from within the country of employment.

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Our client is dedicated to advancing neuroscience and improving patient outcomes through innovative research and clinical excellence. You will join an international CRO with extensive expertise in neuroscience, covering projects from early to late stage of development for a number of pharma and biotech clients.

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As a Medical Director you will pay a pivotal role in shaping clinical research initiatives and enhancing patient care. You will collaborate with multidisciplinary teams to oversee clinical trials, advice, provide support for safety evaluation, develop study protocols, and ensure the highest standards of medical and clinical practice.

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This role can either be part of the multi-project team or you can be embedded in a cutting-edge biotechnology company with whom the CRO is partnering.​

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Responsibilities

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• Provide expert medical oversight and monitoring, as well as leadership for clinical studies, ensuring study teams adherence to protocols, relevant SOPs, client and regulatory requirements. Ensure medical validity of clinical outcomes. 

• Provide medical input, assessment and support to creating key clinical trial documents – creating protocols, clinical study reports (CSRs), safety reports, risk management plans and other documents while implementing the latest scientific information. Contribute to site selection, review and approval of clinical documentation.

• Provide medical review and analysis for trial adverse events. Collaborate with medical and safety teams to process SAEs (Serious Adverse Events).

• Act as the chief medical liaison between the sponsor and internal departments, addressing concerns and correcting issues.

• Oversee patient care within clinical trials, ensuring subject’s eligibility and safety, advising on ethical standards, needed protocol clarifications and safety concerns. Ensure the safety and welfare of study subjects, identifying, and addressing medical issues early. 

• Work closely with internal and external stakeholders, being their medical point of contact. Support principal investigators when needed and collaborate with cross functional study team members on medical issues and risks.

• Ensure all research activities comply with relevant SOPs, applicable regulations and guidelines, including GCP and IRB standards.

• Provide therapeutic and protocol-specific training to study teams. Educates investigator sites by delivering presentations during investigator meetings.

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Requirements 

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• MD (Medical Degree) with board certification in Neurology and active medical licensure.

• 4+ years of experience as a Neurologist.

• Experience as an Investigator in clinical research or other relevant experience in the pharmaceutical industry in clinical development or PV.

• Understanding of pharmacovigilance principles and patient safety in clinical research.

• Excellent leadership and team collaboration skills.

• Comprehensive understanding of regulatory requirements and ICH-GCP guidelines.

• Outstanding analytical, problem-solving, and communication skills, with ability to present data to internal and external stakeholders.

• Ability to travel occasionally for investigator meetings and site visits.

• Full professional proficiency in English. 

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What You Get in Return

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• Competitive Salary and Benefits: Attractive compensation package, including health insurance, pension plans, and more depending on your location.

• Professional Development: Opportunities for continuous learning and career advancement in a supportive, collaborative, and innovative environment.

• Impactful Work: Contribute to groundbreaking research that makes a real difference in patients' lives.

• Collaborative Culture: Join an international team of passionate professionals dedicated to excellence in clinical research.

• Equal Opportunity Employer: Our client celebrates diversity and are committed to an inclusive environment for all employees in all locations.

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How to Apply

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Get in touch with Oli Dimitrov for more information on oli.dimitrov@anttalent.com or call +44 208 135 5914, or click on the apply button to send us your CV or register your interest. We will be in touch as soon as possible.

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Ant Talent - Who We Are

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We are a boutique recruitment agency working closely with select clients in the pharmaceutical industry, focusing mainly on Medical & Regulatory Affairs. We pride ourselves on identifying and recruiting the best professionals for our clients. Do you feel ready to take the next step in your career? We are looking for pioneers, just like you, to help create a healthier world for everyone. And we are here to support you every step of the way.

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