Tallo logoTallo logo

Clinical Research Associate

Job

Greiner AG

Monroe, IA (In Person)

Full-Time

Posted 2 weeks ago (Updated 2 weeks ago) • Actively hiring

Expires 6/1/2026

Apply for this opportunity

This job application is on an outside website. Be sure to review the job posting there to verify it's the same.

Review key factors to help you decide if the role fits your goals.
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
70
out of 100
Average of individual scores

Were these scores useful?

Skill Insights

Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.

Job Description

Your challenge
Responsibility:
  • Monitoring of external and internal clinical performance evaluations and internal clinical trials (development studies, post-marketing complaints/observations)
  • Preparation of relevant documents for clinical trials according to project requirments and internal processes
  • "Preparation of study documents (e.g. templates/protocols)
  • "Review of study documents (e.g. templates/protocols)
  • Performance of site initiations, on-site monitoring, monitoring GBO-lab, remote monitoring and close-out visits
  • Communication with investigators, opinion leaders, consultants, CRO, suppliers
  • Filing of documents, TMF maintainance
  • Training of study team members in accordance with protocol specific requirements and (local) regulations
  • Support the (international) trials submission to authorities and ethics committees
  • Ensuring the accuracy, validity and completeness of study data
  • Trial sites feasibilities
Your Profile Job Requirements:
  • University degree in biology, medicine, pharmacy or an equivalent combination of education, training and work experience in clinical trials
  • At least 2 years of experience as a clinical research associate/ clinical monitor in a CRO/medical device or pharmaceutical company
  • Good knowledge of current industry practices related to the conduct of clinical trials (ICH-GCP, ISO14155, ISO 20916)
  • Good knowledge of MDR and IVDR, as well as good understanding of GDPR
  • Experience with
FDA, ISO
regulations and CLSI guidelines an advantage
  • Ability to work independently and reliably in a fast-paced and changing environment
  • Excellent communication skills are a must
  • Travelling required
  • Driving license We provide equal opportunities for everyone and see diversity as our strength.
Therefore, we welcome all applicants - regardless of identifying characteristics such as gender, age, background, social status, veteran status, sexual orientation, religion, or mental and physical abilities. We have additionally set the goal of empowering women and increasing female leader representation. We foster an inclusive work environment and encourage all individuals to apply.
Job ID:
3278 About Greiner Bio-One Greiner Bio-One feels like home. For visionaries with drive and ideas, for team players who share their knowledge and entertain new ways of thinking, for people who (are able to laugh at themselves and) strive for excellence. Our door is always open to achievers, doers and hidden talents who want to make a difference. We have future in our blood.

Similar remote jobs

Similar jobs in Monroe, IA

Similar jobs in Iowa