Clinical Research Associate II

As a CRA II, 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.

Home-based position from anywhere in Latvia

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
  • Degree in Life Sciences (or similar), or an equivalent combination of education, training & experience
  • At least 3 years of experience conducting independent on-site monitoring visits, ideally on multiple projects at a time
  • Demonstrable experience in all types of monitoring visits in Phase II and/or III
  • Native/Fluent Latvian
  • Strong written and verbal communication skills
  • 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. 
  • Experience supporting Oncology and/or Gastroenetreology studies is an asset

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 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.

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 company founded in 1995, we bring together more than 2,500 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you.

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