Charlotte, NC Clinical Research Specialist Jobs - RSS Feed

Clinical Research Coordinator

Sat, 06 Sep 2008 07:27:49 +5000

A World Wide Clinical Research Organization (CRO) is searching for Site Start Up Specialists and Clinical Research Coordinators (CRC) in the Research Triangle Park of North Carolina.

Job Description:
The Purpose of the Site Start Up/Coordinator (CRC) Specialist position is to provide all necessary support in identifying and selecting investigators, and in completing the collation of all required documentation necessary so that investigational product can be shipped to sites in advance...

Clinical Research Coordinator

Thu, 16 Oct 2008 05:19:11 +5000

A World Wide Clinical Research Organization (CRO) is searching for Site Start Up Specialists and Clinical Research Coordinators (CRC) in the Research Triangle Park of North Carolina.

This candidate will be specifically reviewing Informed Consent Forms (ICF's) within the study start up department.

Job Description:
The Purpose of the Site Start Up/Coordinator (CRC) Specialist position is to provide all necessary support in identifying and selecting investigators, and in completin...

Clinical Research Coordinator

Fri, 10 Oct 2008 04:53:57 +5000

A World Wide Clinical Research Organization (CRO) is searching for Site Start Up Specialists and Clinical Research Coordinators (CRC) in the Research Triangle Park of North Carolina.

This candidate will be specifically reviewing Informed Consent Forms (ICF's) within the study start up department.

Job Description:
The Purpose of the Site Start Up/Coordinator (CRC) Specialist position is to provide all necessary support in identifying and selecting investigators, and in completin...

Clinical Research Coordinator

Fri, 03 Oct 2008 01:27:25 +5000

A World Wide Clinical Research Organization (CRO) is searching for Site Start Up Specialists and Clinical Research Coordinators (CRC) in the Research Triangle Park of North Carolina.

This candidate will be specifically reviewing Informed Consent Forms (ICF's) within the study start up department.

Job Description:
The Purpose of the Site Start Up/Coordinator (CRC) Specialist position is to provide all necessary support in identifying and selecting investigators, and in completin...

Clinical Research Coordinator

Fri, 26 Sep 2008 02:38:42 +5000

A World Wide Clinical Research Organization (CRO) is searching for Site Start Up Specialists and Clinical Research Coordinators (CRC) in the Research Triangle Park of North Carolina.

This candidate will be specifically reviewing Informed Consent Forms (ICF's) within the study start up department.

Job Description:
The Purpose of the Site Start Up/Coordinator (CRC) Specialist position is to provide all necessary support in identifying and selecting investigators, and in completin...

Clinical Research Coordinator

Fri, 19 Sep 2008 04:58:02 +5000

Clinical Research Coordinator

Mon, 15 Sep 2008 06:21:53 +5000

Clinical Research Coordinator

Sat, 06 Sep 2008 06:40:34 +5000

Clinical Research Coordinator Job Description:
A Large Clinical/Investigational Research Center is searching for Clinical Research Coordinator based in Raleigh, NC. Job duties and responsibilities will include but are not limited to the below criteria.

Job Description
Responsible for study related procedures for clinical trials in a large Practice. Candidate will be responsible for contacting enrolled patients for a large clinical study and communicating with them regarding study ...

Regional Clinical Research Associate

Mon, 13 Oct 2008 17:25:31 +5000

One of our clients, a CRO, is looking for a Regional Clinical Research Associate.

This Regional Clinical Research Associate will be home-based and cover sites on the East Coast for a Post-Marketing Study.

This position is a 2 year contract with the possibility to be extended up to 5 years.

Major job duties include:
- Monitoring multiple clinical research sites.
- Follow up with sites via phone and e-mail.
- Responsible for managing regulatory site documents and ...

Regional Clinical Research Associate

Fri, 10 Oct 2008 05:57:41 +5000

A CRO has an immediate need for an experienced Regional Clinical Research Associate.

This Regional Clinical Research Associate will be home-based and cover sites on the East Coast for a Post-Marketing Study. The initial contract is for 2 years and can be extended.

Major job duties include:
- Monitoring multiple clinical research sites.
- Follow up with sites via phone and e-mail.
- Responsible for managing regulatory site documents and binders.
- Training of site staff...

Director of Clinical Research (Device)

Fri, 10 Oct 2008 05:23:21 +5000

A small to medium sized medical device company is seeking a Director or Associate Director to manage its North American clinical operations. The director will design and implement strategies and tactics for completing clinical trials. This person will have 6 or 7 CRAs and support staff reporting to them directly.

Here are some general ideas:
-Planning, initiating and overseeing/conducting monitoring of studies
-Interface with regulatory entities
-Manage budgets
-Data monit...

Regional Clinical Research Associate

Thu, 02 Oct 2008 22:15:55 +5000

Clinical Research Associate

Thu, 16 Oct 2008 05:13:52 +5000

A client of ours that is a Contract Resource Organization (CRO) based out of Indiana is looking for a Clinical Research Associate to cover sites on the East Coast.

*Post marketing phase IV study with 80% travel
*2 year contract

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 an...

Clinical Research Associate

Mon, 06 Oct 2008 22:24:41 +5000

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

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:
-1-2 years of experience as a CRA.
-...

Clinical Research Associate

Fri, 03 Oct 2008 13:46:12 +5000

Clinical Research Associate

Thu, 25 Sep 2008 23:59:25 +5000

A client of ours that specializes in device trials in clinical research is looking for a Clinical Research Associate located on the East Coast to do regional monitoring.

*Phase III study with 5 to 7 sites
*10 month contract

Responsibilities:

- Implementation and monitoring of the clinical trial at selected sites
- Conduct site visits pre-study, study initiations, and to study close out
- Utilizing EDC, but EDC experience not required
- Ensure Case Report Forms (C...

Site Start Up Specialist

Sat, 06 Sep 2008 07:39:25 +5000

Site Start Up Specialist

Mon, 15 Sep 2008 06:21:50 +5000

Site Start Up Specialist

Fri, 19 Sep 2008 04:58:16 +5000

Site Start Up Specialist

Fri, 26 Sep 2008 02:38:38 +5000