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Clinical Research Associate / Senior CRA

extra holidays - extra parental leave
Remote: 
Full Remote
Contract: 
Experience: 
Senior (5-10 years)
Work from: 

Offer summary

Qualifications:

College/University degree in Life Sciences, Independent monitoring experience in Germany, Experience in AMG studies, Phases II and/or III, Expertise in Oncology, Hematology, or Rare Diseases is a plus, Proficient in German, English, and MS Office.

Key responsabilities:

  • Conduct onsite and remote monitoring visits
  • Perform CRF review and query resolution
  • Manage site communication and identification
  • Assist in training lessexperienced CRAs
  • Senior CRA may lead some projects
PSI CRO AG  logo
PSI CRO AG Large https://www.psi-cro.com/
1001 - 5000 Employees
See more PSI CRO AG offers

Job description

Company Description

Why PSI? We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do.  A dynamic, global, mid-size company founded in 1995, we bring together more than 2,700 driven, dedicated and passionate individuals.  We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Job Description

As a CRA at PSI you will be involved in improving patients' lives while enjoying a variety of monitoring tasks and working on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.

Office-based in Munich/Planegg or Home-based in Germany

You will:

  • Conduct and report all types of onsite monitoring visits as well as remote visits.
  • Perform CRF review, source document verification and query resolution.
  • Be responsible for site communication and management.
  • Be involved in site identification process.
  • Assist in training of less expert CRAs, depending on your level of experience.

*Senior CRA can be assigned as Lead Monitor in some projects, while still partially monitoring.

Qualifications
  • College/University degree in Life Sciences or an equivalent combination of education, training & experience.
  • Independent on-site monitoring experience in Germany.
  • Independent experience in all types of monitoring visits in AMG studies, Phases II and/or III.
  • Experience in Oncology, Hematology, Infectious / Rare / Gastro-intestinal Diseases is a plus.
  • Full working proficiency in German, English and MS Office applications.
  • Ability to plan, multitask and work in a dynamic team environment.
  • Communication, collaboration, and problem-solving skills.
  • Ability to travel and valid driver’s license.

Additional Information

As a privately owned mid-size CRO, we are constantly growing, offering plenty of opportunities for personal and professional growth. With no investors to please, our management focuses on company culture and operational delivery over quarter-to-quarter profitability.

Make the right call and take your career to a whole new level. Join a company that focuses on its people and invests in their professional development and success.

Our extensive onboarding and mentorship program will prepare you to fulfil your tasks with the highest standards, offering you:

  • Excellent and flexible working conditions.
  • A unique combination of team collaboration and independent work.
  • Competitive salary and benefits package.

If you'd like to hear more about PSI, our organic growth and company culture, and learn more about the studies that we run and our high repeat and referral business rates, please apply for this vacancy.

Required profile

Experience

Level of experience: Senior (5-10 years)
Industry :
Pharmaceuticals
Spoken language(s):
EnglishGermanEnglish
Check out the description to know which languages are mandatory.

Other Skills

  • Microsoft Office
  • Problem Solving
  • Planning
  • Multitasking
  • Communication

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