Clinical Trial Support Specialist occupation at EDJ Associates, Inc. in Rockville

EDJ Associates, Inc. is at the momment seeking for Clinical Trial Support Specialist on Wed, 11 Jul 2012 16:21:10 GMT. Clinical Trial Support Specialist â€" Blinded Authorizer POSITION TITLE: Clinical Trial Support Specialist LOCATION: Rockville, MD DEPARTMENT: Pharmaceutical Management Branch, Cancer Therapy Evaluation Program ORGANIZATIONAL RELATIONSHIPS: Reports to: Project Director for “NCI Contract” POSITION SUMMARY: The Clinical Trial Support Specialist is responsible for the execution of drug order...

Clinical Trial Support Specialist

Location: Rockville, Maryland

Description: EDJ Associates, Inc. is at the momment seeking for Clinical Trial Support Specialist right now, this occupation will be placed in Maryland. More details about this occupation opportunity please read the description below. â€" Blinded Authorizer

POSITION TITLE: Clinical Trial Support Specialist

LOCATION: Rockville, MD

DEPARTMENT: Pharmaceutical Management Branch, Cancer Therapy Evaluation Program

ORGANIZATIONAL

RELATIONSHIPS:
Reports to: Project Director for “NCI Contract”

POSITION SUMMARY:
The Clinical Trial Support Specialist is responsible for the execution of drug order entry and support duties, essential to the maintenance and functioning on the PMB contract.

ESSENTIAL RESPONSIBILITIES:

• Triage and distribute clinical drug requests for open label and blinded

protocol studies.

• Authorize and process daily clinical drug requests for blinded protocol

studies.

• Analyze orders for accuracy and contact sites for order discrepancies.
• Assist callers with inquires pertaining to blinded drug requests.
• Handle and ensure confidentiality of blinded information for patients.
• Process patient transfers and compile shipping records and/or drug return

receipts.

• Act as liaison between PMB and clinical sites participating on CTEP sponsored

investigational agents.

• Verify patient’s dosage for injection agents by recalculating dose.
• Prepare monthly progress reports for client.

OTHER RESPONSIBILITIES: Working with the Blinded Pharmacists to ensure minimal order entry mistakes are made when entering the clinical drug requests (CDRs) or electronic orders. Working with the sites to ensure the correct information is submitted for the patients. Working with the repository when there are special instructions needed for drug shipments. Providing other support duties as needed for the smooth running of the contract (e.g. faxing, copying, filing, updating of standard operating procedures, data entry, scanning, dissemination of mail, etc.)

QUALIFICATIONS AND REQUIREMENTS:
Education: The successful candidate will have a BS in a Health Science field, or experience with data entry and working with clinical trials. In addition, candidates should have strong attention to detail, the ability to work independently as well as part of a team, and should be self-motivated.

Experience: Data entry experience desired

Skills/Knowledge:

• Good writing and verbal communication skills
• Proficiency with Microsoft Office Suite, especially Word and Excel
• Proficient with the use of office equipment and computers
• Extensive experience with Microsoft Outlook
• Ability to work as part of a team or independently as needed with little

direction or supervision and have the ability to quickly analyze and resolve specific problems

Other: Willingness to work as part of a team and with a diverse group of people is essential. Strong team building and people skills and ability to work under pressure with limited guidance are critical.

Requires manual dexterity sufficient to operate standard office machines such as computers, photo copiers, fax machines, and telephones

Other related duties and tasks as assigned.
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If you were eligible to this occupation, please email us your resume, with salary requirements and a resume to EDJ Associates, Inc..

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This occupation will be started on: Wed, 11 Jul 2012 16:21:10 GMT

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