ASSOCIATE / MEDICAL DIRECTOR, RHEUMATOLOGY

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Are you a board-certified Rheumatologist with a strong interest in clinical research and hands-on experience as an investigator in clinical trials? Are you motivated by working in innovative and fast-moving environments where your medical expertise can contribute to the development of new therapies?​ If so, we encourage you to consider an exciting opportunity with a globally recognised Contract Research Organization (CRO).

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Our client is committed to advancing rheumatology research and improving outcomes for patients through high-quality clinical development programs. In this role, you will become part of a global Medical Affairs team within a CRO that has extensive experience in rheumatology studies, supporting projects across early through late-stage clinical development for a range of biotechnology and pharmaceutical partners.

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As a Medical Director, you will play an important role in guiding clinical trial activities and supporting high standards of patient safety and scientific quality. Working closely with multidisciplinary teams, you will contribute to the oversight of clinical trials, support the development of study protocols, and help ensure that all medical and clinical processes meet the highest professional standards.

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Role & Locations

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This is a full-time, remote (home-based) position that can be based in most European countries, including the UK and Serbia.

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Responsibilities

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• Provide medical leadership and oversight for rheumatology clinical trials, ensuring that study teams follow study protocols, applicable SOPs, sponsor requirements, and regulatory standards. Safeguard the medical integrity of rheumatology clinical endpoints.

• Contribute medical expertise to the preparation and review of key clinical trial documentation, including protocols, clinical study reports (CSRs), safety reports, risk management plans, and related materials, ensuring the integration of current scientific knowledge. Support site selection and review of clinical documentation.

• Perform medical review and evaluation of adverse events, working closely with safety and medical teams in the assessment and processing of Serious Adverse Events (SAEs).

• Serve as a key medical contact between the sponsor and internal departments, helping to resolve medical questions and address potential issues during the course of clinical studies.

• Support oversight of patient safety and eligibility within clinical trials, providing guidance on protocol interpretation, ethical considerations, and emerging safety signals to ensure the well-being of study participants.

• Collaborate with both internal and external stakeholders, acting as the medical point of contact for study teams. Provide support to principal investigators and work with cross-functional teams to address medical questions and potential risks.

• Ensure that all clinical research activities are conducted in compliance with SOPs, applicable regulations, and international guidelines, including Good Clinical Practice (GCP) and IRB requirements.

• Deliver therapeutic area and protocol-specific training to clinical study teams when required.

• Participate in clinical data review, analysis, and reporting, interpreting study findings and preparing reports related to feasibility, safety considerations, and strategic recommendations for stakeholders.

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Requirements 

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• Medical Doctor (MD) with board certification in Rheumatology and an active medical license.

• Minimum 4 years of clinical practice as a Rheumatologist.

• Previous experience as a Principal Investigator (PI) or Sub-Investigator in clinical trials, or relevant experience within the pharmaceutical industry in areas such as clinical development or pharmacovigilance.

• Strong leadership capabilities and the ability to work effectively within cross-functional teams.

• Solid understanding of clinical research regulations and Good Clinical Practice (GCP).

• Excellent analytical thinking, problem-solving, and communication skills.

• Professional-level English proficiency.

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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.

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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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