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

IQVIA; Remote; EUR 50.000 - 70.000; Vollzeit

Zusammenfassung

A global contract research organization is seeking a Clinical Research Associate 2/SrCRA 1 for a home-based position throughout Germany. The ideal candidate will have a degree in life sciences, at least two to four years of on-site monitoring experience, and fluency in German at a C1 level. Responsibilities include performing monitoring visits, ensuring compliance with GCP and ICH guidelines, and mentoring team members. This role offers support for career growth and flexible work schedules.

Leistungen

Home-office

Company car

Accident insurance

Career growth resources

Qualifikationen

• Minimum of two-four years of on-site monitoring experience.
• Strong knowledge of the applicable clinical research regulatory requirements.
• Flexibility to travel 40-60% of working time.

Aufgaben

• Perform site selection, initiation, monitoring, and close-out visits.
• Support the development of a subject recruitment plan.
• Evaluate the quality and integrity of site practices.

Kenntnisse

On-site monitoring experience

Knowledge of GCP and ICH guidelines

Fluency in German (C1 level)

Communication skills

Attention to detail

Ausbildung

University Degree in life science or related field

Health care apprenticeship

Jobbeschreibung

Join IQVIA as aClinical Research Associate 2/ CRA 2or asSenior Clinical Research Associate1/SrCRA 1(m/w/d) and workhome-based throughout Germanyin oursingle 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 topics or additional tasks might be included

Qualifications:

• University Degree inlife scienceor other scientific discipline or apprenticeship in thehealth carefield
• Minimum oftwo-four years of on-site monitoring experiencealternatively 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 Germanon at least C1 level and agood command ofEnglish
• Flexibility to travel up to 40-60% of working time
• Driver’s license class B

What you can expect:

• Resources that promote your career growth
• Leaders that support flexible work schedules
• Programs to help you build your therapeutic knowledge
• Dynamic work environments that expose you to new experiences
• Home-office, company car, accident insurance and more

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

Please apply with your English CV and motivation letter.