Chicago, IL Clinical Research Specialist Jobs - RSS Feed

Clinical Research Coordinator

Fri, 31 Oct 2008 02:51:31 +5000

A Pharmaceutical company has an immediate opening for a Clinical Research Coordinator in Chicago, Illinois.

The Clinical Research Coordinator is responsible for coordinating daily operation of clinical studies and research projects.

Job Duties Include:
-Assists investigators in identifying potential subjects for research studies and utilize appropriate marketing tools.
-Initiates study start-up activities including study initiating meeting and case report forms.
-Phase...

Clinical Research Associate

Mon, 15 Sep 2008 05:53:48 +5000

One of our clients has an immediate opening for a CLINICAL RESEARCH ASSOCIATE in Chicago, Illinois.

The Clinical Research Associate is responsible for monitoring investigator-sponsored clinical studies, from study initiation through final monitoring (close-out) visits.

Job Duties Include:
-Managing study budgets.
-Reviewing CRF's.
-Communication with hospital IRB, NIH, and FDA.
-Writing study protocols.

Job Qualifications:
-3-5 years of experience as a CRA.<...

Clinical Research Associate

Fri, 19 Sep 2008 02:48:35 +5000

Clinical Research Associate

Fri, 26 Sep 2008 00:37:14 +5000

Senior Clinical Research Associate

Thu, 02 Oct 2008 21:36:49 +5000

A Worldwide Clinical Research Organization is searching for an immediate Senior Clinical Research Associate (CRA) based in the North Central Region of the United States. The following experience and expertise are required.

Project Details:

Study/Therapeutic Area: Allergy
Protocols: 1
Phase:III
Travel: 70%
Study Status: Start Up
Site Locations: North central, US
Homebased? Yes
Availability: 1.0,Full-Time
Project Duration: 1+ years

Monitoring Respo...

Clinical Research Associate

Sat, 18 Oct 2008 17:34:33 +5000

A client of ours doing an Allergy study that has an immediate need for a home based Clinical Research Associate located out of Mid West.

*60 to 70% travel

Monitoring Responsibilities:

- Implementation and monitoring of the clinical trial at selected sites
- Conduct site visits pre-study, study initiations, and to study close out
- Ensure Case Report Forms (CRF) are reviewed and completed
- Planning and implementing all activities required to monitor trial and ensur...

Clinical Research Associate

Sat, 18 Oct 2008 17:34:46 +5000

A client of ours doing an Oncology study has an immediate need for a Regional home based CRA in the Mid West.

*60 to 70% travel

Monitoring Responsibilities:

- Implementation and monitoring of the clinical trial at selected sites
- Conduct site visits pre-study, study initiations, and to study close out
- Ensure Case Report Forms (CRF) are reviewed and completed
- Planning and implementing all activities required to monitor trial and ensuring that Good Clinical Prac...

Clinical Research Associate

Sat, 18 Oct 2008 18:35:54 +5000

One of our clients has an immediate opening for a CLINICAL RESEARCH ASSOCIATE in the Mid West.

The Clinical Research Associate is responsible for monitoring investigator-sponsored clinical studies, from study initiation through final monitoring (close-out) visits.

Job Duties Include:
-Managing study budgets.
-Reviewing CRF's.
-Communication with hospital IRB, NIH, and FDA.
-Writing study protocols.

Job Qualifications:
-Oncology Experience
-1-2 years of exp...

Clinical Research Associate

Sun, 26 Oct 2008 04:20:07 +5000

One of our clients has an immediate opening for a CLINICAL RESEARCH ASSOCIATE in the Mid West.

The Clinical Research Associate is responsible for monitoring investigator-sponsored clinical studies, from study initiation through final monitoring (close-out) visits.

Job Duties Include:
-Managing study budgets.
-Reviewing CRF's.
-Writing study protocols.

Job Qualifications:
-2 years of experience as a CRA.

If you are interested in learning more about this o...

Clinical Research Associate

Thu, 16 Oct 2008 13:28:28 +5000

One of our clients has an immediate opening for a CLINICAL RESEARCH ASSOCIATE in the Mid West.

The Clinical Research Associate is responsible for monitoring investigator-sponsored clinical studies, from study initiation through final monitoring (close-out) visits.

Job Duties Include:
-Managing study budgets.
-Reviewing CRF's.
-Writing study protocols.

Job Qualifications:
-GERD experience.
-2 years of experience as a CRA.

If you are interested in learn...

Clinical Research Associate

Mon, 13 Oct 2008 17:25:41 +5000

Clinical Research Associate

Mon, 13 Oct 2008 17:19:09 +5000

Clinical Research Associate

Fri, 10 Oct 2008 03:56:50 +5000

Clinical Research Associate

Fri, 10 Oct 2008 03:55:31 +5000

Clinical Research Associate

Fri, 10 Oct 2008 03:50:21 +5000

One of our clients has an immediate opening for a CLINICAL RESEARCH ASSOCIATE in the Mid West.

The Clinical Research Associate is responsible for monitoring investigator-sponsored clinical studies, from study initiation through final monitoring (close-out) visits.

Job Duties Include:
-Managing study budgets.
-Reviewing CRF's.
-Writing study protocols.

Job Qualifications:
-GERD experience.
-2 years of experience as a CRA.

If you are interested in learn...

Clinical Research Associate

Fri, 10 Oct 2008 03:39:59 +5000

Regional Clinical Research Associate

Thu, 16 Oct 2008 05:27:12 +5000

A large CRO has an immediate need for a Regional Home-Based Clinical Research Associate in the Midwest.

Major job duties and responsibilities:
- Home-Based, Regional Travel.
- Responsible for monitoring ~10 clinical trial sites.
- Responsible for training sites on protocol and other study related issues.
- Perform Pre-Study to Closeout Visits of Clinical Sites.
- Liaise with sites and in-house team.
- Complete trip reports in a timely manner.

Job requirements and ...

Clinical Research Associate/Monitor

Thu, 16 Oct 2008 05:34:04 +5000

Aerotek Scientific is seeking qualified candidates to work for our client in the Pharmaceutical industry as a Clinical Research Associate/Monitor.

*Home based
*Mid west travel
*Must be living in either Chicago, IL, Kansas City, MO or Dallas, TX

QUALIFICATIONS:

-Must have at least 5 years of experience as a Monitor
-Working knowledge of FDA regulations and GCP regulations

RESPONSIBLITIES:

- Monitor clinical sites for adherence to ICH and GCPs.
-...

Regional Clinical Research Associate

Sun, 26 Oct 2008 02:26:30 +5000

Clinical Safety Nurse

Sun, 28 Sep 2008 01:09:35 +5000

A major pharmaceutical company located in the Northern Chicago Suburbs has an immediate need for an Clinical Safety Nurse.

Clinical Safety Nurses are responsible for the review of clinical data, including adverse events and serious adverse events from clinical research trials and post-marketed products. Clinical Safety Nurses work independently with minimal supervision.

Major job duties include:
- Documentation of adverse events and serious adverse events
- Review of clinica...