Saint Paul, MN Clinical Research Specialist Jobs - RSS Feed

Regional Clinical Research Associate

Mon, 15 Sep 2008 06:20:22 +5000

A Mid-Sized Medical Device company with a product line based around septal occluders (used to repair "hole in your heart") with a strong R&D pipeline, reputation and growth has an opening for a Regional Clinical Research Associate in Minneapolis, Minnesota.

The Clinical Research Associate is responsible for monitoring clinical research studies.

Major Job Duties Include:
-Monitor Clinical Research Trials.
-Responsible for study start up and closeout visit...

Regional Clinical Research Associate

Fri, 03 Oct 2008 01:50:08 +5000

A large Pharmaceutical Company has an immediate need for a Regional Home-Based Clinical Research Associate based in Minnesota.

Major job duties and responsibilities:
- Responsible for 10 or more Regional Sites.
- Responsible for training sites.
- Pre-Study to Closeout Visits of Clinical Sites.
- Liaise with sites and in-house team.
- Complete trip reports.

Job requirements and qualifications:
- Must have at least 2 Years of Home-Based CRA Experience.
- Experien...

Senior Clinical Research Associate

Thu, 02 Oct 2008 21:35:00 +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: 60%
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

Mon, 06 Oct 2008 22:38:21 +5000

-Clinical Research Associate will schedule and conduct monitoring activities at assigned centers assessing site compliance to the clinical investigation plan, regulations and GCPs, as needed.
-Responsible for obtaining all relevant source data for adverse events and deaths, as needed.
-Assist in the writing of AE/Death Summaries. Follow-up with any adverse event issues identified by the medical advisor.
-Independently develop and implement corrective and preventive actions at sites a...

Clinical Research Associate II

Thu, 16 Oct 2008 13:29:23 +5000

A large medical device company is looking for a Clinical Research Associate II to join their team. The responsibilities of this candidate are as follows:
-Organizes new clinical studies with limited supervision
-Acts as primary author of clinical study protocols and supporting documents (informed consent, case report forms, training materials, etc)
-IRB and IACUC approval contacts for both human and animal studies

-Primary responsibility for recruitment, selection, and training ...

Clinical Research Associate II

Tue, 23 Sep 2008 18:46:32 +5000

Clinical Research Associate II

Sat, 06 Sep 2008 06:42:50 +5000

Regional Clinical Research Associate

Thu, 16 Oct 2008 05:27:10 +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 ...

Senior Clinical Research Associate

Sat, 06 Sep 2008 07:39:01 +5000

Sr. CRA Job Duties and Description:

- The Sr Clinical Research Associate is a permanent, long term need.
- 30-50% travel, coast to coast, potentially some international.

- The Sr. Clinical Research Associate Duties will include:
- Monitoring
- Pieces of study management
- Protocol writing
- Site initiation thru closeout

- The client is a CRO that specializes in the medical device, IVD, and biologics industries.
- Th...

Clinical Research Associate

Fri, 10 Oct 2008 05:51:06 +5000

-Clinical Research Associate will be working with a new antibacterial IV dressing.
-Clinical Research Associate will be doing standard monitoring as part of this job, but will also be doing site identification, qualification, contract negotiation, set up, and close-out.
-CRA will spend part of their time doing bench microbiology in the lab, working on product they will be monitoring.

-Basic Data management may be part of the job.
-CRA will be working on Post-Market Studies.
...

Clinical Study Manager

Fri, 03 Oct 2008 01:22:25 +5000

The Clinical Study Manager is responsible for managing the development, implementation, and execution of clinical research studies consistent with R&D and Marketing plans, and applicable regulations and policies.

-Clinical Study Manager will assist in the development of the Investigational Plan in consultation with the cross-functional project team, investigators and the clinical team.
-Supports tasks to determine study schedule and objectives.
-Ensures that communication regard...

Director of Clinical Affairs

Thu, 02 Oct 2008 21:47:03 +5000

Responsibilities:
1.Collaborates with cross-functional teams and pharmaceutical partners in the clinical development process.
2.Responsible for managing the selection of vendors in accordance to company s policies and optimal delivery of results. Screen, select and manage Clinical Research Organizations (CRO) and clinical sites.
3. Provides strategic input on issues related to: clinical trial timelines, costs and feasibility.
4.This individual MUST have managed an entire Phase II...

Director of Clinical Affairs

Fri, 26 Sep 2008 00:19:55 +5000

Responsibilities:
1. Director of Clinical Affairs is responsible for the clinical trial operations of combination products utilizing electronic drug delivery platforms. (iontophoresis)
2. Collaborates with cross-functional teams and pharmaceutical partners in the clinical development process.
3. Director of Clinical Affairs is responsible for managing the selection of vendors in accordance to company s policies and optimal delivery of results. Screen, select and manage Clinical ...

Clinical Study Coordinator

Sat, 06 Sep 2008 07:39:04 +5000

Clinical Study Coordinator
-Prepares and maintains investigator files
-Drafts site trial-related correspondence
-Tracks the receipt of required documents from the sites
-Assembles Regulatory Binders and Patient Binders

-Clinical Study Coordinator will produce periodic standard reports for the CRA and the sites
-Creates purchase orders for clinical trial payments, office supplies and printing needs
-Facilitates the payment processing by creating check requests, back-up do...

Research Assistant

Fri, 26 Sep 2008 02:54:57 +5000

A Research Technician opening is available at a widely recognized pre clinical research facility for medical devices.

Candidates Must Have:
*A two or four year degree
*1 year of research experience
*Experience with SOP's and GLP's
*Certification (for Veterinary Technicians)

Main Responsibilities Include:
*Assists in supporting surgical procedures, including surgical preparation, anesthesiology, pre and post-operative care, other routine animal care
*Operates, main...

Market Research Analyst

Sat, 06 Sep 2008 06:41:29 +5000

Our client is currently in need of an individual to come in and assist in business development to help identify new markets, create financial documentation, and work with electronic databases within the Biotech industry. Ideal candidate has three plus years of experience in biotech setting. Qualified applicants need only apply. Required Skills for Market Research Analyst Job: BUSINESS DEVELOPMENT PHARMA MEDICAL DEVICE INTELLECTUAL PROPERTY MARKET RESEARCH FINANCIAL ANALYSIS About Aerotek S...

Research Assistant I

Fri, 31 Oct 2008 02:52:09 +5000

There is an immediate need for a Research Assistant I at a company that provides microbiology and virology efficacy testing services to clients who develop antimicrobial and products.

Minimum Requirements:
* Bachelors Degree in Biology or related field.
* 1+ year of Microbiology in the industry; specifically with Aseptic Technique
* Must be detail oriented and high attention to detail

Responsibilities:
* Performs chemical and germicidal efficacy testing utili...

Regulatory Affairs Specialist

Thu, 02 Oct 2008 23:29:45 +5000

We are looking for experienced Regulatory Affairs professionals looking for a new opportunity. The responsibilities of this positions include:
-Develop and implement global regulatory registration and support strategies throughout the life cycle of products
-Perform device classification/predicate device search and global regulatory standard search and management
-Develop product modification/line extension strategies and management
-Perform proactive data and information collectio...

Regulatory Affairs Specialist

Mon, 06 Oct 2008 22:36:53 +5000

-Regulatory Affairs Specialist is responsible for managing the regulatory aspects of projects/products, including the preparation and submission of correspondences and applications to regulatory agencies.
-Functions as a direct liaison with regulatory authorities and facilitates the review and approval process of applications.
-Leads and/or participates in project team meetings, by providing regulatory support to ensure compliance with all FDA requirements.
-Regulatory Affairs Specia...

Regulatory Affairs Specialist

Sat, 18 Oct 2008 18:36:55 +5000