CRA for Observational/ Non-interventional study
- Employer
- Parexel
- Location
- Hoersholm, Denmark
- Salary
- Competitive
- Start date
- 28 Feb 2023
- Closing date
- 30 Mar 2023
View more
- Discipline
- Clinical Research, Clinical Trials Manager / Administrator
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
Job Details
We believe in our values; Patients First, Quality, Respect, Empowerment & Accountability.
Due to a growing portfolio, we are currently looking for experienced monitors (CRA) for Observational/ Non-interventional study to be based in Nordics with knowledge of the Local language and regulatory requirements .
In this role you will Independently provide site management and support activities for Observational/ Non-interventional research study sites in accordance with relevant Standard Operating Procedures (SOPs), study-specific procedures and regulations.
Responsibility for protocol expertise with accountability for quality and timelines and the following site start-up activities:
•Site identification
•Negotiation of site agreements and budgets
•Collection and review of regulatory documents for EC and RA submissions
•Customization of informed consent
•Site management.
Knowledge and Experience:
- Clinical Monitoring, Data Management and/or research experience with a solid understanding of Observational/ Non-interventional research methodology and terminology.
Skills:
- Excellent interpersonal, verbal and written communication skills in English (and local language as necessary - fluency in either Finnish, Swedish, Danish or Dutch).
- Strong computer skills, familiar with MS-Office products including Excel, Word and PowerPoint, Clinical Trial Management and EDC systems.
- Thorough knowledge of Observational/ Non-interventional study research and relevant regulations including GPP.
- Ability to work in a 'virtual' team environment as well as work independently, seeking guidance as appropriate.
- Seeks opportunities to develop experience and knowledge making suggestions to enhance service delivery.
Education :
- Degree in a life science, nursing qualification or other relevant experience required.
In return we will be able to offer you a structured career pathway and development within the role including awareness and understanding of the industry. Your hard work will be rewarded with a competitive base salary as well as a benefits package including holiday per year, pension scheme as well as other leading edge benefits that you would expect with a company of this type.
If you are ready to join Parexel's Journey, please apply!
Company
When you join us, you’re joining a team that sees everything they do as an opportunity to transform the world for patients everywhere. When our employees bring their many perspectives together to tackle a new challenge, there’s no limit to what they can accomplish. Through it all, at the center of all we do, is a patient whose life could change – forever. And together, we’ll do it With Heart™.
How to describe Parexel’s culture in one word:
Working With Heart™ - Christina's perspective:
Careers Blog | Our Culture | Diversity, Equity & Inclusion | Benefits | Our Hiring Process
Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help lifesaving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory, and therapeutic expertise, our team of more than 21,000 global professionals works in partnership with biopharmaceutical leaders, emerging innovators, and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere.
- Website
- http://www.parexel.com/
- Telephone
- +44 1895 238000
- Location
-
The Quays
101-105 Oxford Road
Uxbridge
Middx
UB8 1LZ
United Kingdom
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