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CRA for Observational/ Non-interventional study

Employer
Parexel
Location
Hoersholm, Denmark
Salary
Competitive
Start date
31 Mar 2023
Closing date
30 Apr 2023

Job Details

Parexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our therapeutic, technical, and functional ability is underpinned by a deep conviction in what we do.

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

Parexel International Corporation is a leading global biopharmaceutical services organization, providing a broad range of knowledge-based contract research, consulting, and medical communications services to the worldwide pharmaceutical, biotechnology and medical device industries. Committed to providing solutions that expedite time-to-market and peak-market penetration, Parexel has developed significant expertise across the development and commercialization continuum, from drug development and regulatory consulting to clinical pharmacology, clinical trials management, medical education and reimbursement. Parexel Informatics, Inc., a subsidiary of Parexel, provides advanced technology solutions, including medical imaging, to facilitate the clinical development process.

 

Mission: Parexel’s mission is to combine the strength of our expertise, experience and innovation to advance the worldwide success of the bio/pharmaceutical and medical device industries in preventing and curing disease.

 

Company info
Website
Telephone
+44 1895 238000
Location
The Quays
101-105 Oxford Road
Uxbridge
Middx
UB8 1LZ
GB

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