Clinical Research Associate 2 or Senior Clinical Research Associate 1 (m/w/d), Single Sponsor

IQVIA Inc; Frankfurt; Remote; EUR 55,000 - 90,000; Full time

Benefits offered by this job

Home-office

Flexible schedules

Competitive salary

Company car or car allowance

Pension plan

Job summary

IQVIA is seeking a Clinical Research Associate 2 (CRA 2) or Senior Clinical Research Associate 1 (SrCRA 1) to join our single sponsor department, working home-based across Germany.

The role offers exposure to diverse therapeutic areas, training and mentoring, and a clear path for career growth. You will conduct site visits, monitor progress, and ensure GCP/ICH compliance while collaborating with study teams and client representatives.

Qualifications

• University degree in life sciences or health-care apprenticeship.
• 2–4 years on-site monitoring experience.
• Knowledge of GCP/ICH regulatory requirements.
• Strong written and verbal communication and attention to detail.
• Fluency in German at C1 and good command of English.
• Willingness to travel up to 40–60%.
• Driver’s license class B.

Responsibilities

• Performing site visits, initiation, monitoring and close-out visits.
• Supporting the development of a subject recruitment plan.
• Ensuring regulatory compliance and data quality per GCP/ICH.
• Tracking regulatory submissions, recruitment, CRF completion and data queries.
• Collaborating with site staff and client representatives.
• Possible remote-monitoring and involvement in start-up processes.

Skills

German (C1)

English proficiency

Communication skills

GCP/ICH knowledge

Driver’s license (B)

Education

Life sciences degree or healthcare apprenticeship

Job description

Join IQVIA as a Clinical Research Associate 2 / CRA 2 or as Senior Clinical Research Associate 1 / SrCRA 1 (m/w/d) and work home-based throughout Germany in our single sponsor department.

You will enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our clients.

Whether you're just starting out or looking to deepen your expertise, this role promises to offer intentional career growth and professional development. With access to world-class training and mentoring, you’ll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas.

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.
• Depending on client model there might be remote-monitoring, involvement in study start-up processes, specialization on therapeutic area (pharmaceutical product or medical devices).
• Mentoring of less experienced team members, support as subject matter expert for specific tasks or additional tasks might be included.

Qualifications

• University Degree in life science or other scientific discipline or apprenticeship in the health care field.
• Minimum of two-four 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 travel up to 40-60% of working time.
• Driver’s license class B.

What You Can Expect

• Permanent employment contract.
• Home-office and flexible working schedules.
• Competitive salary
• Company car or car allowance, accident insurance, pension and more.
• Resources that promote your career growth.

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.