Freelance Senior Clinical Research Associate at PSI CRO

Bratislava, Region of Bratislava, Slovakia -

Full Time

Start Date

Immediate

Expiry Date

30 Jun, 26

Salary

0.0

Posted On

01 Apr, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research, Monitoring, Data Compliance, Site Management, Regulatory Support, Feasibility Research, Oncology Studies, MS Office

Industry

Pharmaceutical Manufacturing

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 in Slovakia. 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 Full and clean driver's license, and the ability to travel. Fluency in Slovak and English Experience supporting Oncology studies is beneficial, but not essential Intermediate to Advanced knowledge of MS Office 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.

Responsibilities

As a Senior CRA, you will ensure timelines, targets, and standards of clinical research projects while building relationships with clinical sites and investigators. You will focus on subjects' rights, safety, and quality of data compliance.