Clinical Research Associate (CRA)

SanaClis s.r.o.

Place of work
Prague, Czechia
Contract type
full-time
Start date
to be agreed, ASAP

Information about the position

Job description, responsibilities and duties

We are looking for an experienced and committed CRA with great communication skills, critical thinking and attention to detail.

You will be responsible for monitoring clinical trials and ensuring that:
- Clinical Trial is conducted, recorded, and reported in accordance with all applicable international and local regulations and guidelines, good practices, SOPs and Clinical Trial Protocol.
- Data quality and integrity meet acceptable clinical standards.
- Rights and safety of patients involved in a study are protected.

You will also serve as facilitator of Clinical Trial conduct in respective area (country) in terms of identifying qualified sites and investigators, facilitating communication between Sponsor and regulatory authorities and trial sites.

Employee perks, benefits

We are an equal opportunities employer, in terms of gender and age. We create family friendly environment offering flexible working time, home based work.
Our CRAs have generally only 1 or 2 projects assigned and the travel time is limited to 40% of working time.

Other employee benefits will be specified during job interview.

Information about the selection process

A successful candidate must have:
Knowledge of clinical research processes and medical terminology.
Expert knowledge of ICH GCP and Regulatory requirements.
3-5 years of experience in clinical trial industry on a position of CRA - experience with oncology trials is much preferred.
Willingness and ability to travel domestically and internationally, as required.

Requirements for the employee

Candidates with education suit the position

University education (Bachelor's degree)
University education (Master's degree)
Postgraduate (Doctorate)

Educational Specialization

preferred qualification in nursing, life sciences or medical sciences

Language skills

English - Upper intermediate (B2) and Czech - Advanced (C1)

Driving licence

B

Number of years of experience

3
3

Personality requirements and skills

We are looking for a resilient, self-motivated, driven, and result oriented person, who is able to overview the whole picture as well as focus on details.
Strong and effective written and verbal communication skills are a must.
A good candidate must also have very good time management and organization skills, and be able to plan and meet timelines, and prioritize effectively.

Advertiser

Brief description of the company

SanaClis is a full-service European CRO offering a comprehensive range of services for clinical trials. In additional to being a full-service CRO, SanaClis is one from very few CROs in the world who has in-house logistics capabilities. This includes QP services, customs brokerage, warehousing and distribution, and sourcing of clinical trial materials, comparators and rescue medication.

Company address

SanaClis s.r.o.
Stare Grunty 130
84104 Bratislava
Slovakia

Contact

Kontaktní osoba: Kristina Okkelova
Tel.: +421917098314
E-mail: poslat životopis
ID: 3793164  Datum zveřejnění: 25.3.2021