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

IQVIA

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

IQVIA

Frankfurt, Hesse, Germany

·

On-site

·

Full-time

·

2w ago

Benefits & Perks

Flexible Hours

Remote Work

Learning Budget

401(k)

Healthcare

Flexible Hours

Remote Work

Learning

401k

Healthcare

Required Skills

Clinical research

GCP knowledge

ICH guidelines

German language

English language

Join IQVIA as a Clinical Research Associate 1or Clinical Research Associate 2/ CRA I or CRA II 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 topics 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 12 month of on-site monitoring 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 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.

  • Dynamic work environments that expose you to new experiences.

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

Please apply with your English CV and motivation letter as well as your education certificates and job reference letters (Arbeitszeugnisse).

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

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About IQVIA

IQVIA

IQVIA

Public

Focused on health information technology and clinical research.

10,001+

Employees

Durham

Headquarters

$17B

Valuation

Reviews

3.9

2 reviews

Work Life Balance

2.5

Compensation

2.0

Culture

2.8

Career

3.0

Management

2.5

65%

Recommend to a Friend

Pros

Structured feedback and development process

Meaningful contribution to client businesses

Problem-solving with specialized knowledge

Cons

Strict performance requirements and termination risk

High-level rubric definitions lack detail

No performance bonuses offered

Salary Ranges

42 data points

Junior/L3

Senior/L5

Junior/L3 · Analyst

2 reports

$107,910

total / year

Base

$93,834

Stock

-

Bonus

-

$97,750

$118,068

Interview Experience

3 interviews

Difficulty

3.0

/ 5

Duration

14-28 weeks

Experience

Positive 0%

Neutral 33%

Negative 67%

Interview Process

1

Application Review

2

HR Screen

3

Hiring Manager Interview

4

Technical Manager Interview

5

Executive/GM Interview

6

Offer

Common Questions

Behavioral/STAR

Case Study

Technical Knowledge

Past Experience

Culture Fit