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Senior Clinical Research Associate at PSI CRO AG

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

Offer summary

Qualifications:

College degree in Life Sciences, Independent on-site monitoring experience in Romania, Experience in Phase II and/or III monitoring, Proficient in MS Office applications, Full working proficiency in English.

Key responsabilities:

  • Conducting onsite monitoring visits
  • Managing site communication and activities
  • Performing CRF reviews and query resolution
  • Supporting quality control and compliance
  • Assisting in the training of junior CRAs
PSI CRO AG  logo
PSI CRO AG Pharmaceuticals Large https://www.psi-cro.com/
1001 - 5000 Employees
See more PSI CRO AG offers

Job description

Company Description

PSI is a leading Contract Research Organisation with more than 25 years in the industry, offering a perfect balance between stability and innovation to both clients and employees.  We focus on delivering quality and on-time services across a variety of therapeutic indications.

Job Description

As a Senior CRA, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. Your focus will be on subjects’ rights, safety and well-being and quality of data compliance.

Your responsibilities will include:

  • Conducting and reporting all types of onsite monitoring visits
  • Driving the study startup phase (if applicable)
  • Performing CRF reviews, source document verification and query resolution
  • Be responsible for site communication and management
  • Supervising study activities, timelines and schedules for each site
  • Acting as a point of contact for in-house support services and vendors
  • Supporting quality control, such as compliance monitoring and reports review
  • Participating in feasibility research
  • Assisting in training of less experienced CRAs

Qualifications
  • College/University degree in Life Sciences or an equivalent combination of education, training & experience
  • Independent on-site monitoring experience in Romania
  • Experience in all types of monitoring visits in Phase II and/or III
  • Experience in Oncology, Hematology, Infectious / Rare / Gastro-intestinal Diseases, Multiple Sclerosis is a plus
  • Full working proficiency in English
  • Proficiency in MS Office applications
  • Ability to plan, multitask and work in a dynamic team environment
  • Communication, collaboration, and problem-solving skills
  • Ability to travel

Additional Information

What We Offer:

  • Stability, long-term cooperation
  • Permanent contract, full-time job
  • Hybrid or home-based work setting
  • Competitive salary and benefit package
  • Career development 
  • Unique combination of team collaboration and independent work
  • Friendly and supportive colleagues
  • Onboarding courses about clinical research industry
  • Mentoring and on-the job training
  • Comfortable and well-established modern office

This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.

Required profile

Experience

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

Other Skills

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

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