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CRA II FLORIDA REGIONAL CLINICAL RESEARC
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CRA II FLORIDA REGIONAL CLINICAL RESEARCH ASSOCIATE
Skills:
CRA II FLORIDA REGIONAL CLINICAL RESEARCH ASSOCIATE
Date:
5-1-2008
Location:
Orlando, FL
Area code:
407
Tax term:
FULLTIME
Pay rate:
$75,000.00 - $85,000.00 per year
Length:
Perm
Position ID:
5251
Dice ID:
10200902
Job description:
REGIONAL CLINICAL RESEARCH ASSOCIATE CRA II - FLORIDA
PHARMACEUTICALS
WE ARE SEARCHING FOR A FULL TIME CLINICAL RESEARCH ASSOCIATE II IN FLORIDA TO WORK FROM HOME SUPPORTING CANCER / ONCOLOGY / UROLOGY FIELD CLINICAL TRIAL RESEARCH - IS THAT YOU?
This is a Permanent Direct Hire Position
What are we looking for ?
A Clinical Research Associate [CRA] experienced in Oncology or Urology related pharmaceutical research (2-3 yrs. field trials) on the Sponsor side, who can work from their home / virtual office by assisting with coordination of clinical studies within the Clinical Operations area while demonstrating initiative and originality in organizing, systematizing and coordinating activities.
MUST HAVE:
1-BA or BS degree
2-Clinical research oncology or urology experience
3- 2+ years of direct clinical monitoring experience. This must be on the sponsor side (Pharma) monitoring and traveling to multiple sites. (Working in a hospital is NOT sufficient)
Our client is a leading edge biopharmaceutical company that acquires, develops and commercializes a diversified portfolio of oncology and other drug candidates that meet critical health challenges for which there are few other treatment options.
The company's pipeline includes promising early and late-stage drug candidates with unique formulations and mechanisms of action that address the needs of seriously ill patients, such as at-home chemotherapy and new treatment regimens for refractory disease. The passion of the company to identify, develop and deliver better options for people suffering from cancer is behind every action they take.
What 's in it for you?
Generous compensation, great people and a magnificent health, dental, vision, life, AD&D, and long-term disability insurance package, as well as Paid Vacation/Personal Days and a 401k plan with matching Company stock.
Responsibilities:
Demonstrate superior communication and organizational skills in addition to the technical skills required for overseeing clinical studies.
Recognize the urgency of meeting established schedules and be able to prioritize tasks and time to meet those schedules.
Help manage and report on the conduct of clinical studies, as directed.
Help identify and select trial sites.
Conduct qualification, initiation, interim monitoring close-out visits, and perform drug accountability (approximately 50% travel required).
Ensure the timely collection of appropriate regulatory documents from study sites.
Develop materials that support the conduct of clinical studies including:
site reference manuals, monitoring flow sheets, CRF completion guidelines, etc.)
Review clinical documents for accuracy and completion (1572, informed consents, protocols, meeting minutes, etc).
Assist in the preparation of investigator's meetings.
Participate as a member of project teams and coordinate efforts of other areas of the Company to support clinical project schedules.
Remain current with applicable regulations concerning development and conduct of human clinical trials (CFRs, ICH). Communicate to investigators the rudiments of GCP and their related responsibilities.
Demonstrate working knowledge of relevant clinical trial SOPs. Draft or revise Clinical SOPs as directed.
Ensure assigned studies adhere to approved protocols.
Maintain a level of accuracy that minimizes data query rate and ensures data are accurately transcribed to meet SOP and audit expectations. Identify and provide solutions for data trends.
Support other team members and facilitate team cohesion; play an active role in personal training and development needs.
Desired Experience
Requirements
Skills, Education and Experience:
MUST HAVE:
1-BA or BS degree
2-Clinical research oncology or urology experience
3- 2+ years of direct clinical monitoring experience. This must be on the sponsor side (Pharma) monitoring and traveling to multiple sites. (Working in a hospital is NOT sufficient)
Experience in Industry Sponsored Trials
Minimum BA or BS degree with 2 years direct clinical monitoring experience.
Have a broad understanding of clinical research.
Have a working knowledge of the relevant SOPs.
Have the necessary interpersonal and communication skills to establish professional working relationships with colleagues and site personnel.
MS Word, Excel, in-depth knowledge of other presentation programs a plus.
Strong, organizational planning and follow-through skills.
Excellent language and grammar skills, ability to write clearly and concisely.
Attention to detail and the ability to prioritize.
Ability to work well under pressure and with tight schedules.
Ability to plan and schedule workload and work effectively with others.
Ability to exercise judgment within generally defined practices and policies for obtaining data.
Self-direction and motivation are mandatory.
Other Desired Skills: CRA II FLORIDA REGIONAL CLINICAL RESEARCH ASSOCIATE
Minimum Education Required: Bachelor
Years of Experience Required: At Least 3 Years
Expected Travel Time: About 25%
Travel required:
unspecified
Telecommute:
no
Click Here to Apply
Applicant Category: Professional
Requisition Code: Work at home
Two Initials of Recruiter: bw
System Date: 05/01/2008
System Time: 15:42:25
Document Name(40): CRA II FLORIDA REGIONAL CLINICAL RESEARC
Source: Dice Tech Jobs - USA
SearchTerms: "work at home" "work from home"
URL(80): http://seeker.dice.com/jobsearch/servlet/JobSearch?op=302&dockey=xml/0/b/0b396d0
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