Senior Clinical Research Associate job in North Chicago, USA

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First Name*

Last Name*

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Phone Number*

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Are you an employer or a jobseeker?*

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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?*

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Job type: Contract

Discipline: Clinical Research Associate (CRA), Project/Study Manager (CSM/CPM), Clinical Scientist

Location: United States

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

Proclinical is currently recruiting for a Senior Clinical Research Associate with a global biopharmaceutical company located in North Chicago, IL. Successful candidate will be responsible for supporting the planning and execution of one or more Phase I-IV clinical research studies.

Job Responsibilities:

Responsible for executing one or more elements of clinical studies in compliance with quality standards (ICH/GCP, Global Regulations, and internal policies and procedures).
Support the Study Project Manager in leading the cross functional study team.
Support the preparation of Clinical Study Team meetings (Agenda/Minutes).
Responsible for regular updates to the cross-functional team and stakeholders on study status; ensure our CTMS is up to date.
Support the development of the clinical study blueprint/protocol and associated systems and documents (Informed consent forms, eCRFs, IRT, CSR).
Support the vendor selection, scope development, management and oversight of external vendors in compliance with internal processes and procedures and the applicable regulations.
Responsible for generating the study related training for the study team, study sites, and vendors for assigned studies.
Proactively identify and resolve and/or escalate study related issues.

Skills and Requirements:

Bachelor's or equivalent is required, typically in nursing or scientific field; or RN by Associate's degree with relevant experience is acceptable.
Must have at least 4+ of Pharma-related/clinical research related experience and demonstrated a high level of core and technical competencies.
Possesses good communication skills.
Competent in application of standard business procedures {Standard operating procedures, International Conference on Harmonization {ICH), Global Regulations, Ethics and Compliance).
Preferred exposure to study initiation through study completion.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please call Amanda Rivera at (+1) 267-435-8555 or upload your resume on our website - www.proclinical.com.

A full job description is available on request.

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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