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Senior Clinical Research Associate

Role overview

Qualifications

  • BSc or MSc in Life Sciences (or similar), or equivalent education, training and experience
  • Independent on-site monitoring experience in Slovakia, ideally on multiple projects
  • Strong written and verbal communication skills
  • Fluency in Slovak and English

Responsibilities

  • 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

Key facts

Other skills

  • Quality Control
  • Communication
  • Problem Solving
  • Collaboration
  • Multitasking

About the company

PSI CRO AG  logo

PSI CRO AG

Contract Research Organizations (CRO)

PSI is a leading full-service global Contract Research Organization whose key strength is predictable patient enrollment across multiple therapeutic areas. PSI is known in the industry as a CRO focused on ‘on-time project delivery’. This is achieved through investing substantial effort and MD resources into performing quality feasibility assessments that provide an accurate predictor of study timelines. PSI’s global reach allows us to run clinical trials across multiple continents, in 50+ countries around the world. PSI’s reputation is that of a 'no-nonsense' CRO focused on timely patient enrollment and project delivery. An exceptionally high repeat and referral business rates alongside low staff turnover are indicative of our commitment to be the best CRO in the world as measured by our clients and our employees. http://www.psi-cro.com

Company details

Company typeLarge
IndustryContract Research Organizations (CRO)
Company size1001 - 5000

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Job description

Company Description

PSI is a leading Contract Research Organisation with 30 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.

This is a freelance (contractor) home-based position

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
  • Supporting the regulatory team in preparing documents for study submissions and regulatory approval

Qualifications

  • BSc or MSc in Life Sciences (or similar), or an equivalent combination of education, training & experience
  • Independent on-site monitoring experience in Slovakia, ideally on multiple projects at a time
  • Demonstrable experience in all types of monitoring visits in Phase II and/or III
  • Strong written and verbal communication skills
  • Fluency in Slovak and English
  • Experience supporting Oncology studies is beneficial, but not essential
  • Intermediate to Advanced knowledge of MS Office
  • Ability to plan, multitask and work in a dynamic team environment
  • Communication, collaboration, and problem-solving skills are essential
  • As you will be monitoring multiple sites, you must have a full and clean driver's license, and the ability to travel. 

Additional Information

Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success. Our recruitment process is easy and straightforward, and we’ll be there with you every step of the way. We will guide and support you with information, making your experience as smooth as possible.

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MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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