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Clinical Research Associate
SanaClis s.r.o.
Place of work
Prague, Czechia (Job with occasional home office)
Prague, Czechia (Job with occasional home office)
Contract type
full-time
full-time
Wage (gross)
65 000 Kč/monthThe salary will be based on mutual agreement and will reflect the seniority level of an applicant
65 000 Kč/monthThe salary will be based on mutual agreement and will reflect the seniority level of an applicant
Information about the position
Job description, responsibilities and duties
We Are Hiring!
We are looking for an experienced CRA to strengthen our clinical operations in the Czech Republic. Full time employment with working from home option.
Job Requirements:
· Bachelor’s degree required – preferred qualification in nursing, life sciences (biology, microbiology, toxicology, biochemistry, or pharmacology) or medical sciences (physiology, immunology, medicine, anatomy, or pharmacy)
· Minimum 2 years of experience and experience in oncology is a must
· Profound knowledge of clinical research processes and medical terminology
· Expert knowledge of ICH GCP, and international and local regulatory requirements
· Passion for clinical research
· Driving license B
Job Responsibilities:
You would be primarily 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
- Ensuring data quality and integrity meet acceptable clinical standards
- Guaranteeing the rights and safety of patients involved in a study are protected
- Performing and coordinating all aspects of the clinical monitoring and site management process
- Conducting remote and on-site visits to assess protocol and regulatory compliance and managing required documentation
- Developing collaborative relationships with investigational sites, act as a site processes specialist, ensuring that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects rights, well-being, and data reliability; and you would ensure audit readiness.
- Serving as facilitator of Clinical Trial conduct in respective area in terms of identifying qualified sites and investigators, facilitating communication between sponsor and regulatory authorities and trial sites.
We are looking for an experienced CRA to strengthen our clinical operations in the Czech Republic. Full time employment with working from home option.
Job Requirements:
· Bachelor’s degree required – preferred qualification in nursing, life sciences (biology, microbiology, toxicology, biochemistry, or pharmacology) or medical sciences (physiology, immunology, medicine, anatomy, or pharmacy)
· Minimum 2 years of experience and experience in oncology is a must
· Profound knowledge of clinical research processes and medical terminology
· Expert knowledge of ICH GCP, and international and local regulatory requirements
· Passion for clinical research
· Driving license B
Job Responsibilities:
You would be primarily 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
- Ensuring data quality and integrity meet acceptable clinical standards
- Guaranteeing the rights and safety of patients involved in a study are protected
- Performing and coordinating all aspects of the clinical monitoring and site management process
- Conducting remote and on-site visits to assess protocol and regulatory compliance and managing required documentation
- Developing collaborative relationships with investigational sites, act as a site processes specialist, ensuring that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects rights, well-being, and data reliability; and you would ensure audit readiness.
- Serving as facilitator of Clinical Trial conduct in respective area in terms of identifying qualified sites and investigators, facilitating communication between sponsor and regulatory authorities and trial sites.
Employee perks, benefits
· Competitive salary
· Flexible working hours and home-based working option
· Great work-life balance (our CRA's are not overwhelmed with projects as we believe in quality over quantity)
· Performance and Retention Bonus
· Use of Company Car and Mileage Allowance
· Career growth and development opportunities in a continuous learning culture
· Friendly environment in a privately owned international company
· Additional paid day off on your birthday
· Other company benefits based on mutual agreement
*SanaClis is an equal opportunity and inclusive employer
· Flexible working hours and home-based working option
· Great work-life balance (our CRA's are not overwhelmed with projects as we believe in quality over quantity)
· Performance and Retention Bonus
· Use of Company Car and Mileage Allowance
· Career growth and development opportunities in a continuous learning culture
· Friendly environment in a privately owned international company
· Additional paid day off on your birthday
· Other company benefits based on mutual agreement
*SanaClis is an equal opportunity and inclusive employer
Requirements for the employee
Candidates with education suit the position
University education (Master's degree)
Postgraduate (Doctorate)
Postgraduate (Doctorate)
Educational Specialization
life sciences
Language skills
English - Upper intermediate (B2) and Czech - Advanced (C1)
Driving licence
B
Experience in the position/sector
active clinical monitoring experience is required, including monitoring of oncology trials. We expec
Number of years of experience
2
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.
ID: 4361662
Datum zveřejnění: 22.6.2022
2022-06-22
lokalita: Prague Pozice: Clinical Research Associate Společnost: SanaClis s.r.o.
Spodní hranice mzdy (brutto): 65 000 Kč/month