Medical Manager Czech Republic and Slovakia

Recordati

Prague, CZ Onsite Regulatory & Medical Affairs

About this role

Job Purpose

Lead and drive Medical Affairs activities across the Czech Republic and Slovakia by developing and implementing the local medical strategy, providing scientific and medical leadership, ensuring compliance with applicable regulations and ethical standards, and supporting the generation and communication of scientific evidence throughout the product lifecycle.

Key Responsibilities

Develop, coordinate and implement the Medical Affairs strategy and annual medical plan for CZ & SK
Provide medical and scientific expertise for assigned products and therapeutic areas
Lead, coordinate and support the Medical Affairs team (2 MSLs CZ, 1 MSL SK)
Build and maintain relationships with KOLs, healthcare professionals, investigators, scientific societies and academic institutions
Generate, analyse and communicate medical insights to support strategic decision-making
Review and oversee the scientific accuracy, quality and compliance of medical and scientific materials
Support clinical studies, observational studies, Real World Evidence projects and other evidence-generation initiatives
Collaborate closely with Commercial, Marketing, Market Access, Regulatory Affairs, Pharmacovigilance, Compliance, Legal and regional/global Medical Affairs teams
Ensure all medical activities are conducted in line with legal, regulatory, ethical and internal requirements
Identify and escalate medical, regulatory, safety and compliance risks

Required Education

University degree in Medicine or Pharmacy

Required Skills and Experience

Minimum 5 years of relevant experience in the pharmaceutical industry, preferably within Medical Affairs.
Experience in medical strategy development and implementation.
Experience in engagement with the scientific and healthcare community.
Experience in scientific review of materials.
Experience coordinating cross-functional projects.
Experience in team leadership.
Knowledge of the healthcare, scientific and regulatory environment in the Czech Republic and Slovakia.
Experience in clinical programmes, evidence generation, publications or medical education is an advantage.

Technical Competencies

Very good knowledge of Medical Affairs processes.
Strong understanding of clinical research and evidence generation.
Knowledge of regulatory, ethical and compliance requirements.
Ability to critically evaluate scientific literature.
Ability to interpret complex clinical data.
Proficiency in standard office, communication and medical systems.

Required Behaviours and Competencies

Strategic and analytical thinking.
Scientific integrity and high ethical standards.
Patient-focused mindset.
Strong leadership and team development skills.
Ability to set priorities and coordinate activities across two markets.
Excellent communication and presentation skills.
Strong facilitation, organisational and project management skills.
Ability to make independent and responsible decisions.
Ability to work effectively in multidisciplinary and multicultural environments.

Required Languages

Fluent written and spoken English.
Fluent Czech or Slovak.
Ability to communicate professionally in both Czech and Slovak scientific and healthcare environments.

At Recordati we believe in people! Inspired by our purpose - unlocking the full potential of life - we are committed to creating a diverse environment and cultivating a culture of inclusion. We strive to continually lead with our values and beliefs, enabling our employees to bring their whole selves to work and develop their potential.

We are proud to be an equal opportunity employer. We recruit, develop and reward without regard to, amongst others, gender, sexual orientation, gender identity or expression, national origin, age, physical or mental ability, race, ethnicity, political or religious belief.

If you are looking to join a company where you can try new things, speak openly, and be bold, we invite you to apply today.