Clinical Research Medical Advisor - Czech Republic

Job Description Summary

As a Clinical Research medical Advisor (CRMA) you will support one of designated therapeutic this capacity you will be accountable for all country clinical/medical aspects associated with Development and prioritized Research programs/trials by providing clinical strategic and tactical leadership as the Country Clinical Development representative. (This may involve work across several countries).

It is a bridge between Global Development Study Site Operations (SSO) clinical trials and Medical Affairs aligning technical operations & strategy and Patient Engagement.

CRMAs gather inform and act on clinical/medical/scientific insights for clinical trial concept sheets/protocols Informed Consent Forms (ICFs) and other relevant clinical documents to optimize clinical trial implementation. They also drive the identification and involvement of qualified investigators with the greatest recruitment potential identifies clinical recruitment hurdles and drives clinical recruitment activities to overcome these hurdles.

Working in close collaboration with other country functions (e.g. clinical trial operations Medical Affairs and Patient Engagement) you will actively contribute to successful allocation fast clinical trial start-up timely recruitment early identification of potential delays and development and implementation of mitigation plans.

This position is part of the CRMA GDD team and reports directly to CRMA Cluster Head Central Europe.

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Job Description

Major Accountabilities

• Validating study designs and making the final decision on the clinical/medical trial and program feasibility of implementing a clinical trial protocol based on medical/clinical practice and analysis of the competitive environment in the country.

• Actively contributing to scientific/clinical/medical aspects of the start-up phase to ensure fast clinical trial site start-up.

• Providing scientific/clinical/medical expertise to clinical trial operations team members and during interactions with Country/Cluster external Experts (e.g. Regulatory Authorities Medical Experts Advisory Boards Patient Advocacy Groups ERB/EC etc.).

• Developing clinical/medical trial plans taking the broader ecosystem into account for assigned programs/trials to ensure successful trial implementation.

• Supporting and partnering with internal Stakeholders and internal decision boards as needed regarding clinical trials as the scientific/clinical/medical expert (important internal stakeholders will be Clinical Trial Team Regulatory Affairs Medical Information Medical Affairs Marketing Patient Access Health Economics and Outcomes Research (HE&OR) clinical trial operations etc.)

• Gathering informing and acting on insights from clinical trial Investigators/site staff Medical Experts patients and payers with internal Stakeholders at the Country/Cluster level with the goal to optimize clinical trial implementation.

• Carrying accountability for adherence to safety standards clinical data quality for the Country/Cluster and provides general scientific/clinical/medical support for safety issues

Essential Requirements:

• Scientific degree M.D. Ph.D. or Pharm.D. (M.D. is preferred) ideally with experience in clinical development within the pharmaceutical industry or clinical practice.

• Fluent Czech and English language skills (full proficiency in speaking and in writing)

• Sound understanding of the overall clinical development process and ICH/GCP principles.

• Excellent communication networking and stakeholder management skills

• Agility to move quickly across different therapeutic areas and indications as well as ability to prepare and deliver high quality presentations.

• Willingness to travel up to 50% including internationally (and possibly to other countries in Europe)

Desirable Requirements:

• Subspecialty training.

Why Novartis

Our purpose is to reimagine medicine to improve and extend peoples lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here:

Some restrictions on flexible working options may apply and will be discussed during interview if applicable

You will receive:

Monthly pension contribution matching your individual contribution up to 3% of your gross monthly base salary; Risk Life Insurance (full cost covered by Novartis); 5-week holiday per year (1 week above the Labor Law requirement) ; 4 paid sick days within one calendar year in case of absence due to sickness without a medical sickness report; Cafeteria employee benefit program choice of benefits from Benefit Plus Cafeteria in the amount of 17500 CZK per year; Meal vouchers in amount of 105 CZK for each working day (full tax covered by company); Transport Allowance; MultiSport Card Employee Share Purchase Plan.

Find out more about Novartis Business Services: to Diversity and Inclusion:

Novartis is committed to building an outstanding inclusive work environment and diverse teams representative of the patients and communities we serve.

Accessibility and accommodation:

Novartis is committed to working with and providing reasonable accommodation to all individuals. If because of a medical condition or disability you need a reasonable accommodation for any part of the recruitment process or in order to receive more detailed information about the essential functions of a position please send an e-mail toand let us know the nature of your request and your contact information. Please include the job requisition number in your message.

Skills Desired