Clinical Research Associate 2 (m/w/d), IQVIA Biotech, home-based in Germany

IQVIA; Frankfurt; Hybride; EUR 70 000 - 90 000; Plein temps

Avantages offerts par ce poste

Home office

Flexible work schedules

Company car

Résumé du poste

IQVIA Biotech partners with biotech and biopharma companies to support clinical development across all phases. The role focuses on on-site monitoring, regulatory alignment, and site collaboration, with a permanent contract and flexible work schedules.

The candidate will conduct visits, support recruitment planning, ensure GCP/ICH compliance, and travel up to 40–60% while collaborating with global experts. A life sciences degree or healthcare apprenticeship is required.

Qualifications

• University degree in life sciences or healthcare field or apprenticeship.
• Minimum of two years of on-site monitoring experience.
• Knowledge of GCP and ICH guidelines.
• Strong written and verbal communication skills; attention to detail.
• Fluency in German at C1 level and good English.
• Willingness to travel 40–60% of time.
• Driver’s license class B.

Responsabilités

• Perform site selection, initiation, monitoring and close-out visits.
• Support development of a subject recruitment plan.
• Assess site practices for compliance with GCP/ICH guidelines.
• Track regulatory submissions, recruitment, CRF completion and data queries.
• Collaborate with study sites and client representatives.
• Mentor less experienced team members and provide SME input.
• Potential opportunities to gain experience in Austria or Switzerland.

Connaissances

Site monitoring

Clinical research knowledge

German (C1) & English

Regulatory compliance

Travel readiness

Formation

University degree in life sciences or healthcare apprenticeship

Outils

GCP / ICH familiarity

Description du poste

IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure, collaborative culture, and deep therapeutic expertise allow us to deliver tailored solutions that help bring innovative treatments to patients faster.

Your responsibilities will include:

• Performing site selection, initiation, monitoring and close-out visits.
• Supporting the development of a subject recruitment plan.
• Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution.
• Collaborating with experts at study sites and with client representatives.
• Mentoring of less experienced team members, support as subject matter expert for specific topics or additional tasks might be included.
• Besides focusing on projects in Germany, there may be the opportunity to gain experience in Austria or Switzerland.

Qualifications:

• University Degree in life science or other scientific discipline or apprenticeship in the health care field.
• Minimum of two years of on-site monitoring experience alternatively an equivalent combination of education, training and experience.
• Knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Strong written and verbal communication skills, attention to detail and ability to work in a fast pace environment.
• Fluency in German on at least C1 level and a good command of English.
• Flexibility to conduct business travel up to about 40-60% of working time.
• Driver’s license class B.

What you can expect:

• Permanent contract.
• Home-Office and flexible work schedules.
• Company car, accident insurance and more.
• Resources that promote your career growth.

We invite you to join IQVIA.

Whatever your career goals, we are here to ensure you get there!

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact.

No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere.

Thank you for your interest in growing your career with us.