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8 days old

Clinical Research Associate

Kelly Services
Mettawa, IL 60048
Kelly Services has been providing outstanding employment opportunities to the most talented individuals in the marketplace. We are proud to offer a long-term temporary opportunity to work as a **Clinical Research Associate** at a prestigious Fortune 500 company working in **Mettawa, IL.**





**Important information:** This position is recruited for by a remote Kelly office, not your local Kelly branch. To be considered for this position, you must use the Submit Resume button to submit your resumes. If you have questions about the position, you may contact the recruiter for this position ( Brooke.Schoen@kellyservices.com ) however your resume must be received via the Submit Resume button included within.





**Job Title: Clinical Research Associate**





**Pay: $42 per hour**





**Responsibilities** :

Member of the global medical affairs evidence solutions medical research support team (clinical team) responsible for processing the intake, review, contracting, activation, conduct and closeout of Investigator Initiated Research and External Collaborative Research studies within Global Medical Affairs.


Responsible for assisting Medical Research Supervisor and Evidence Leads in the preparation for scientific medical review of concept and protocol submissions. Provide oversight to approved studies, assuring timely enrollment of patients and retrieval of required document from investigators/study sites, processing workflow status within the study submission and study maintenance system, coordinate drug shipments, prepare payments, receive and route study publications and CSR, perform study closeout activities.


Responsible for executing all elements of externally sponsored research in compliance with quality standards (ICH/GCP, Global Regulations, (e.g., drug supply management, ICBs, reviews and approves HCP invoices/ payments against executed contracts) with minimal oversight and guidance.

Responsible for management of clinical essential documents and critical regulatory documents for assigned projects/studies to ensure document packets for study start-up are complete and accurate and consistent with the study start-up timeline.

Routinely interact with Evidence Leads on assigned projects and in meetings.

Supports the preparation of Scientific Review Meetings (Agenda/ Meeting Materials).

Supports on audit/ inspection activities for GCP requirements.

Responsible for regular updates appropriate for cross-functional team and stakeholders on study status; ensure our CTMS is up to date.

Participates in process improvement initiatives.


**Qualifications**

At least 4-6 years pharma related research experience

Bachelor's degree

Knowledge of externally sponsored research (IIS, external research collaborations)

Knowledge of clinical study execution

Knowledge of Good Clinical Practices and ICH/Guidelines, and/or other Global Regulations

Excellent organizational skills, attention to detail, and strong oral and written communications skills




**Top Skills** :

1. Multitasking

2. Microsoft Skills

3. Organized

What is a nice to have (but not required) regarding skills, requirements, experience, education, or certification? Pharma background clinical trails, univiersity hospital,







**We invite you to bookmark our Web site and encourage you to review it regularly for new opportunities worldwide:** www.kellyservices.com at http://www.kellyservices.com/ **.**



**_Kelly Services is a U.S.-based Fortune 500 company. With our global network of branch locations, we are uniquely positioned to provide our customers with international staffing support and our employees with diverse assignments around the world._**



**Kelly Services is an Equal Opportunity Employer**








**Why Kelly** **** **?**



Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire talented people just like you. Every day, we match science professionals with dream jobs that fit their skills and interestsits the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background/education in science, so we know a thing or two about the science market and how to get you noticed.




**About Kelly** ****



At Kelly, were always thinking about whats next and advising job seekers on new ways of working to reach their full potential. In fact, were a leading advocate for temporary/non-traditional workstyles, because we believe they allow flexibility and tremendous growth opportunities that enable a better way to work and live. Connecting great people with great companies is what we do best, and our employment opportunities span a wide variety of workstyles, skill levels, and industries around the world.


Kelly is an equal opportunity employer committed to employing a diverse workforce and providing accommodations for people with disabilities in all parts of the hiring process as required under its Employment Accommodation Policy. Kelly will work with applicants to meet accommodation needs that are made known to Kelly in advance.

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Posted: 2020-10-12 Expires: 2020-11-12

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Clinical Research Associate

Kelly Services
Mettawa, IL 60048

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