Clinmed, part of NEUCA Group, having 13 years’ experience with investigational medicinal products and medical devices studies we have developed know-how to be very efficient in conducted projects. ClinMed’s extensive understanding of the IMP and medical device regulatory issues enables our clients to save time and money with their studies. Our medical device experts have U.S. FDA as well as European regulatory experience and are flexible to address wide variety client’s demands.
Clinical Research Associate (CRA)
Miejsce pracy: Warszawa
Region: mazowieckie
Numer referencyjny: CRA/08/2019/W
Region: mazowieckie
Numer referencyjny: CRA/08/2019/W
Tasks:
- conduct of all types of monitoring visits to clinical sites in accordance with the Protocol, Standard,
- operating Procedures (SOPs), Good Clinical Practice (GCP) and the applicable Regulatory requirements,
- communication with sponsor, investigators, vendors,
- maintenance of appropriate documentation regarding clinical site management,
- quality control, preparation for and attendance at company’s audits,
- training of investigators and clinical trial team members.
Requirements:
- medical or life science education (medicine, pharmacy, biology or similar),
- 2-5 years of CRA experience,
- knowledge of ICH-GCP guidelines,
- good English skills, both spoken and written,
- excellent communication and interpersonal skills,
- good computer skill,
- desire and ability to travel.
We care about our people as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career. We offer job for full FTE, flexible working arrangemen (Permanent– Home/Office based). We are also looking for candidates not based in Warsaw.