Find FL Research Associate jobs - FL Area Job Search for Research Associate jobs (page 1)

Displaying 1-10 of 962 results

Research Associate III: sanofi pasteur - Orlando, Florida; Science; Performs research activities and other tasks as necessary in a laboratory environment. Records observations and measurements and reports results. Familiar with a variety of the field's concepts, practices, and procedures. Relies on extensive experience and judgement to plan and accomplish goals. Performs a variety of tasks, including conducting studies using established protocols, aiding in the development of novel protocols and methods, and some presentation of data (written and oral). May lead and direct the work of others. A wide degree of creativity and latitude is expected. Adheres to (see more)

Research Associate: Magnus Research Consultants, Inc. - Ft. Lauderdale, Florida; Science; Trial and Jury Consulting firm seeks a career minded person is needed to join a busy and growing firm with demanding clients. This position requires extensive travel and long work days, including weekends. Minimum requirements: B.A. or B.S. in psychology or sociology; statistics proficiency; computer expertise including SPSS, WordPerfect, & MS Office; technical skills including video recording, and supervisory/management experience are also required. The Research Associate is responsible for setting up research projects, including travel and facility planning, supervising research staff (see more)

Research Associate II: Moffitt Cancer Center - Tampa, Florida; Science; The Research Associate II assumes the responsibility of performing basic or biological science research within the specified research program. The Research Associate II has responsibility to the faculty of the specified program. See Job Description (see more)

Clinical Research Associate: Confidential - Miami, Florida; Science; JOB TITLE: Clinical Research Associate (CRA) DEPARTMENT: Clinical Operations REPORTS TO: Clinical Project Manager/Senior Project Manager JOB LOCATIONS: Houston, Miami, Phoenix and Raleigh (total of 4 openings; looking for candidates that currently reside in these cities) SUMMARY: The Clinical Research Associate (CRA) is responsible for interfacing with investigative sites to monitor the conduct and assess the progress of clinical research studies to ensure compliance with the protocol and applicable company or Sponsor Standard Operating Procedures (SOPs), FDA regulations, and ICH-GCP (see more)

Clinical Research Associate II (1 of 2): Johnson & Johnson Family of Companies - Florida; Science; Vistakon, a member of the Johnson & Johnson Family of Companies is recruiting for a Clinical Research Associate II located in Jacksonville, FL. VISTAKON, a division of Johnson & Johnson Vision Care, is a worldwide company with operations in the United States, Japan, Latin America, Asia-Pacific and Europe/Middle East/Africa regions. Research, innovation and new-product development are the focus of our organization. Since we introduced soft disposable contact lenses in 1988, no other manufacturer has matched the aggressive expansion of our wide-ranging ACUVUE family of products. Our associates (see more)

Clinical Research Associate II: SciStaff Services - Florida; Science; Our client, a global leader in the pharmaceutical industry, is seeking a Clinical Research Associate to join their Jacksonville, FL, location. This is an on-site position The CRA will plan and monitor human clinical trials in compliance with internal procedures, ICH Guidelines, Good Clinical Practices (GCP) and applicable Regulations and Guidelines. Responsibilities will include: Coordinate protocol and case report form development and compilation. Ensure appropriate clinical trial agreements are signed and materials are distributed. Monitor and secure protocol and regulation compliance at (see more)

Clinical Research Associate: Netsource, Inc. - Florida; Science; Please note this is a 3 month contract position. Skills: Pharma/Biotechnology, BS Degree (MUST have a degree), CRA experience The CRA will plan and monitor human clinical trials in compliance with internal procedures, ICH Guidelines, Good Clinical Practices (GCP) and applicable Regulations and Guidelines. Temp to hire; plenty of potential for growth; MUST have a degree; Coordinates protocol and case report form development and compilation. Insures appropriate clinical trial agreements are signed and materials are distributed. Monitors and secures protocol and regulation compliance at (see more)

Test and Evaluation Research Associate: Riverside Research - Florida; Science; Test and Evaluation Research Associate Summary: Riverside Research's Education and Training Directorate has a full time opening in the Dayton area for Test and Evaluation Research Associate. The candidate will assist with the execution of research targeted at transitioning ideas developed by customer into usable deliverables for external clients. This includes analyzing data, authoring research articles for publication in peer-reviewed journals, presenting at technical conferences, and expanding/developing original research methodologies. Duties and Responsibilities: (see more)

Test and Evaluation Research Associate: Riverside Research - Florida; Engineering; Test and Evaluation Research Associate Summary: Riverside Research's Education and Training Directorate has a full time opening in the Dayton area for Test and Evaluation Research Associate. The candidate will assist with the execution of research targeted at transitioning ideas developed by customer into usable deliverables for external clients. This includes analyzing data, authoring research articles for publication in peer-reviewed journals, presenting at technical conferences, and expanding/developing original research methodologies. Duties and Responsibilities: (see more)

Clinical Research Associate I: Covance - Daytona, Florida; Pharmaceutical; Business Title Clinical Research Associate IRequisition ID 33934BRJob Category Clinical ResearchLocations USA - Daytona Beach, FLShift 1Job Posting The Clinical Research Associate I is trained to conduct site monitoring responsibilities for Clinical Trials, according to Covance Standard Operating Procedures, ICH guidelines and GCP, including Pre-study qualification, Initiation Meetings, Routine, Interim monitoring Visits and Close-out Visits.Duties and Responsibilities:Participates, conducts or assists with the following duties as consistent with training completed:. Assists with the (see more)

Displaying 1-10 of 962 results

* The accuracy of search results can be improved by using quote marks around phrases.

First name:

Last name:

Primary job category:

Country:

Zip code:

Email Address:

Confirm Email Address:

Password:

Confirm Password:

Yes! I would like to receive email alerts on jobs that match my profile and free information on managing my career and job search.

Find FL Area Jobs