Clinical Research Associate

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BITRIAL Kft.
Munkavégzés helye

1121 Budapest, Tállya utca

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Ft/hó Megnézem

Munkaidő, foglalkoztatás jellege
- Alkalmazotti jogviszony
- Általános munkarend
Biztosított eszközök
- Laptop
- Mobiltelefon
- Céges autó
Elvárások
- Angol felsőfok
- Pályakezdő/friss diplomás
- Főiskola
- 'B' kat. jogosítvány

Állás elmentve

A hirdetést eltávolítottuk a mentett állásai közül.

A hirdetés adatait sikeresen elküldte az email címére.

Responsibilities

Conduct different types of monitoring visits (pre-study visits, site initiation visits, interim monitoring visits & close out visits)
Develop and maintain site and investigator relationships to ensure clinical trials are managed efficiently
Perform source document verification and prepare monitoring visit reports, including confirmation and follow-up letter
Manage the study documentation and other essential trial related documents
Support regulatory submissions to the Competent Authority
Participate in Investigator selection/feasibility process

Requirements

University degree in health or naturaé science related field
CRA experience is an advantage
Excellent verbal and written communication skills in English and Hungarian
Valid driving license
Demonstrated flexibility in schedule and willingness to travel on a regular basis
Ability to respond quickly to changing demands and opportunities
Detail-oriented and efficient in time management
Advanced skills and experience using Microsoft Office (Word, Excel, Power Point, Outlook)
Knowledge of czech, slovak, polish, or romanian language is an advantage

What we offer

As a Clinical Research Associate you will have the unique opportunity to have an exciting career in the field of drug and medical device development as part of an expanding team.

Workplace extras

Cafe
Shower
Corporate events
Bicycle storage
Parking
Free fruits, snacks
Free coffee, soft drinks
Free lunch

Company info

BiTrial Clinical Research is a privately owned mid-sized Clinical Research Organization (CRO), based in Central and Eastern Europe (CEE) with a headquarter in Budapest, Hungary. We provide broad range of clinical research services for companies in Pharma, Biotech and MedTech industry and for global CRO’s to support phase I-IV drug and device development, including project management, clinical monitoring, scientific and medical support, investigator and patient recruitment, site management, statistical analysis, data management, drug safety, quality assurance, regulatory and ethics committee affairs and medical writing.

How to apply

We are looking forward to receiving your application with your professional CV in English indicating your salary expectation (monthly, net) via "Jelentkezem" button underneath!

Jelentkezem MENTÉS