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Clinical research coordinator

Jena
Apsida Life Science
Coordinator
Inserat online seit: Veröffentlicht vor 3 Std.
Beschreibung

Apsida Life Science have partnered with a leading research company to present the following role:

Job Title: Clinical Research Coordinator

Location : Jena Germany

Duration - 18 months

Immediate Hire

Company Overview:

The client company is a leading clinical trial company that provides a gold standard platform of clinical trial services designed to work together in synergy, bringing trials closer to patients, making trials faster, more efficient, more inclusive and more accessible for all patients and for all research sites around the world.

Responsibilities Include:

* To support the clinical research teams with ongoing conduct of studies under the oversight of the Principal Investigator (PI), including but not limited to:
* Process blood, test urine samples and other biological samples.
* Entering data into the electronic Case Report Form (eCRF).
* Working with the Clinical Research Associate (CRA) to resolve queries.
* To assist project teams with study specific documentation as appropriate.
* Completion of paperwork such as Case Report Forms (CRFs/eCRFs) and Data Clarification Forms (DCFs).
* To be familiar with the role of the Clinical Research Associate (CRA) and to attend site visits, if appropriate. Work with the CRA to resolve queries
* To maintain the study files and databases for the project.
* To co-ordinate ordering/dispatch and tracking of trial materials.
* Maintaining standards of professional competence and current practices in accordance with ICH-GCP, Research Governance Framework, EU Clinical Trials Directive EU2001/20EC, Good Clinical Practice and the Regulatory Requirements in Germany.
* Provide support and facilitate with study visit scheduling
* Provision of excellent standards of service provision in accordance with study protocol training and country specific requirements.

Key Requirements

* Previous experience as a research site study coordinator or similar role is mandatory. This experience should include a high level of confidence in source documentation and data entry
* Experience specifically with iMedidata EDC is preferred
* Experience with handling lab samples, including processing & shipping, is mandatory and a current IATA training certificate is preferred.
* Cardiology experience is preferred.
* Current (within last year) ICH-GCP certification mandatory.
* Healthcare/sciences background desirable.
* Bilingual proficiency in English and German is mandatory.

Qualifications:

* Relevant Life Science Degree
* Good Clinical Practice Certification
* IATA training certificate is preferred

If you are interested in learning more, please reach out to Mufaro Mpofu:

mufaro.mpofu@apsida.com

Apsida Life Science is a specialist recruitment business based in London (UK), Redhill (UK), Boston (USA) & Pretoria (South Africa) that is dedicated to delivering the best talent to the Life Science industry. We believe there is a gap in the market for a cost effective, high quality and trusted recruitment service that puts the candidate journey at the heart of the recruitment process

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