Experienced Clinical Research Associate (m/w/d), Multi-Sponsor, Germany
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Join IQVIA as an Experienced CRA (m/w/d) in our Clinical Site Management department home-based throughout Germany. You will focus on a comprehensive clinical trial management in a variety of indications and learn about the diverse scientific approach of the sponsors. Beside establishing strong relationships with the global study team and the involved investigators, you will conduct monitoring on complex clinical trials for different pharma companies and assure their adherence to good clinical practices and study protocols.
With strategic site relationship managers supporting you throughout your role, this is a fantastic opportunity for you to embed yourself in the wider clinical operations team and work on ground-breaking new medicine development.
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 on study sites and client representatives.
Qualifications:
University Degree in life science or other scientific discipline or apprenticeship in health care.
Minimum of one year of on-site monitoring experience, alternatively miminum one year experience as Study Coordinator/CTC etc.
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.
Fluent command of German and English.
Flexibility to business travel up to 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/car allowance, accident insurance, pension and more.
Whatever your career goals, we are here to ensure you get there!
Please apply with your English CV and motivation letter.
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.
Job details
How this role compares
Computed from every other active Clinical Research role in our database, not just this employer's listings.
We currently track 133 comparable Associate Clinical Research roles across 17 biopharma companies.
Salary context
25 of 133 peers report a salary range (USD, annualized)
Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.
Where these roles are based
Top locations among the 133 comparable roles
+ 26 more countries
Seniority mix
133 of 133 peers have a known seniority level
Therapeutic area mix
13 of 133 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
Open in 2 locations
Open in 2 locations
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How we calculate "similar"
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Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.