Senior Clinical Research Associate job in Copenhagen, Denmark

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First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

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Job type: Permanent

Discipline: Clinical Research Associate (CRA)

Location: Denmark

This vacancy has now expired. Please see similar roles below...

Proclinical Staffing are partnered with an established CRO currently looking for an individual to join their team. This role is on a permanent basis located in Denmark. The opening position is for an Experienced Clinical Research Associate.

Responsibilities:

Work alongside and mediate with study team members for project implementation assistance when suitable.
You might be responsible for site financial management rendering to implemented clinical trial agreement and retrieve invoices rendering to local needs.
Collaborate with sites to adapt, drive and track subject recruitment plans aligned with project requirements to advance predictability.
The ideal candidate will administer protocol and linked study training to allocated sites and form routine lines of communication with sites to manage current project expectations and concerns.
Review the quality and integrity of study site practices connected to suitable performance of the protocol and adherence to suitable guidelines.
Accountable for escalating quality problems when suitable.
Other duties may be assigned to this role.

Key Skills and Requirements:

Expertise on therapeutic area and protocols offered by the business training.
Computer literacy.
Communication skills both verbally and in writing.
Fluency in English and Danish.
Educated to a high school diploma or degree level in a scientific or healthcare field.
Corresponding mix of training, education and experience might be taken into consideration.
Completion of CRA training program or prior supervisory experience.
Know-how of implementing, suitable clinical research regulatory needs such as GCP and international conference on harmonisation regulations.
An organised individual with the ability to resolve issues.
Able to manage own time efficiently as well as financial management.
Capable of forming and upholding efficient working relationships with others.

If you are having difficulty in applying or if you have any questions, please contact Auxanne Rameix at +44 203 954 7011.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

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