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CTA – Clinical Trial Administrator
Labcorp
Place of work
Bratislava
Bratislava
Contract type
full-time
full-time
Wage (gross)
2 083 - 2 250 EUR/month
2 083 - 2 250 EUR/month
Information about the position
Job description, responsibilities and duties
A formula for clinical innovation: Labcorp Drug Development. With comprehensive drug development services and de-identified data from 70 million patients worldwide, our 60,000 employees advance life-changing medicines across a wide range of therapeutic areas – improving health and lives every day.
If you are looking for a position in which you can leverage your organizational skills and your clinical expertise as much as your talent to connect and communicate with a wide variety of people, this is the perfect opportunity! Join us and see why more than 90% of the top 20 global pharmaceutical companies are repeat customers.
Your responsibilities:
• Support project teams in the full spectrum of clinical research activities such as study start up, site management / closure, document management (eTMF and paper-based), regulatory and site start-up responsibilities, meeting planning
• Coordinate internal and external stakeholders, facilitating smooth processes and top quality
• Administrative support of various contract teams including approvals, quality assurance and document management (contract databases and / or paper-based)
• Set up and maintain clinical investigator files and documentation
• Prepare investigator budget payments and tracking systems; generate tracking reports
• Enter and maintain data into selected study tracking databases and ensure a high level of data quality
• Prepare monitoring visit documentation for CRAs, Project Managers etc.
• Oversee appropriate archiving of study documents and other materials
If you are looking for a position in which you can leverage your organizational skills and your clinical expertise as much as your talent to connect and communicate with a wide variety of people, this is the perfect opportunity! Join us and see why more than 90% of the top 20 global pharmaceutical companies are repeat customers.
Your responsibilities:
• Support project teams in the full spectrum of clinical research activities such as study start up, site management / closure, document management (eTMF and paper-based), regulatory and site start-up responsibilities, meeting planning
• Coordinate internal and external stakeholders, facilitating smooth processes and top quality
• Administrative support of various contract teams including approvals, quality assurance and document management (contract databases and / or paper-based)
• Set up and maintain clinical investigator files and documentation
• Prepare investigator budget payments and tracking systems; generate tracking reports
• Enter and maintain data into selected study tracking databases and ensure a high level of data quality
• Prepare monitoring visit documentation for CRAs, Project Managers etc.
• Oversee appropriate archiving of study documents and other materials
Employee perks, benefits
What you can expect from us:
• permanent employment contract with Labcorp Drug Development
• highly competitive compensation packages
• regular, merit-based salary adjustments
• significant employer contribution to an attractive pension scheme
• extensive insurance coverage, including medical, life, short as well as permanent disability and accidents
• excellent training and career development opportunites as well as support with furthering your education
• strong support from Line Management and more than 20'000 colleagues worldwide
• the world's most renowned pharmaceutical companies as our satisfied, repeat customers for many years
• permanent employment contract with Labcorp Drug Development
• highly competitive compensation packages
• regular, merit-based salary adjustments
• significant employer contribution to an attractive pension scheme
• extensive insurance coverage, including medical, life, short as well as permanent disability and accidents
• excellent training and career development opportunites as well as support with furthering your education
• strong support from Line Management and more than 20'000 colleagues worldwide
• the world's most renowned pharmaceutical companies as our satisfied, repeat customers for many years
Requirements for the employee
Candidates with education suit the position
Follow-up/Higher Professional Education
University education (Bachelor's degree)
University education (Master's degree)
University education (Bachelor's degree)
University education (Master's degree)
Language skills
English - Advanced (C1)
Personality requirements and skills
Education/Qualifications:
• Degree or completed vocational training (office management, administration, health care, life science or similar preferred) or equivalent professional experience
Experience:
• First experience in a comparable role including clinical trial activities
• Familiarity GCP
• Proficient user of IT applications such as MS Office (including strong MS Excel skills) and clinical IT applications (e.g. Veeva Vault)
• Strong organizational and project management skills with a keen attention to detail and a high sense of accountability
• Excellent communication skills in business fluent English – verbal and written – and strong interpersonal skills are a must
• Degree or completed vocational training (office management, administration, health care, life science or similar preferred) or equivalent professional experience
Experience:
• First experience in a comparable role including clinical trial activities
• Familiarity GCP
• Proficient user of IT applications such as MS Office (including strong MS Excel skills) and clinical IT applications (e.g. Veeva Vault)
• Strong organizational and project management skills with a keen attention to detail and a high sense of accountability
• Excellent communication skills in business fluent English – verbal and written – and strong interpersonal skills are a must
Advertiser
Brief description of the company
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ID: 4243445
Posting date: 21.1.2022
2022-01-21
location: Bratislava Position: Clinical Research Associate, Regulatory Affairs Specialist Company: Labcorp
Basic salary component (gross): 2 083 EUR/month