Clinical Trial Feasibility/Operations Consultant

3 weeks ago

Pleasanton, United States Abacus Service Corporation Full time
JOB DESCRIPTION:

The Clinical Trial Feasibility/Operations Consultant will work with a team under direct supervision of the Director of Clinical Trials Planning and Infrastructure. The specific duties may include:
" Determine study activities related to clinical trial protocols.
" Estimate costs related to clinical trial activities and negotiate with sponsors.
" Must demonstrate excellent organizational, interpersonal, and communication skills
" Other duties as required to assist launching clinical trials.

Work Days: Scheduled days and hours are contingent upon departmental needs. Normal schedule: M-F (8:00am 5:00pm).

Work Location: Pleasanton, CA

Basic Qualifications:
" Bachelor's degree

Additional Requirements:
" Must demonstrate excellent organizational, interpersonal, and communication skills.
" Experience with implementing/coordinating clinical trials
" Familiarity with medical terminology
" Must be able to work in a Labor/Management Partnership environment.

Preferred Qualifications:
" Must be dependable, punctual, detail-oriented, and able to follow detailed protocols precisely.
" Experience with research administration.
" Must be able to work successfully with a wide variety of internal and external project staff and research participants
" Must exhibit a professional manner with a high degree of courtesy, tact, and sensitivity.
" Must be able to work well independently as well as part of a larger multi-disciplinary research team.
" Experience with word-processing and spreadsheet software programs preferred.
" Proficiency with Microsoft Office products (Word, Excel, and PowerPoint) and Adobe Acrobat software highly desirable. Actual Job Title Clinical Trial Feasibility/Operations Consultant Additional Job Details JOB DESCRIPTION:

The Clinical Trial Feasibility/Operations Consultant will work with a team under direct supervision of the Director of Clinical Trials Planning and Infrastructure. The specific duties may include:
" Determine study activities related to clinical trial protocols.
" Estimate costs related to clinical trial activities and negotiate with sponsors.
" Must demonstrate excellent organizational, interpersonal, and communication skills
" Other duties as required to assist launching clinical trials.

Work Days: Scheduled days and hours are contingent upon departmental needs. Normal schedule: M-F (8:00am 5:00pm).

Work Location: Pleasanton, CA

Basic Qualifications:
" Bachelor's degree

Additional Requirements:
" Must demonstrate excellent organizational, interpersonal, and communication skills.
" Experience with implementing/coordinating clinical trials
" Familiarity with medical terminology
" Must be able to work in a Labor/Management Partnership environment.

Preferred Qualifications:
" Must be dependable, punctual, detail-oriented, and able to follow detailed protocols precisely.
" Experience with research administration.
" Must be able to work successfully with a wide variety of internal and external project staff and research participants
" Must exhibit a professional manner with a high degree of courtesy, tact, and sensitivity.
" Must be able to work well independently as well as part of a larger multi-disciplinary research team.
" Experience with word-processing and spreadsheet software programs preferred.
" Proficiency with Microsoft Office products (Word, Excel, and PowerPoint) and Adobe Acrobat software highly desirable. Feeder Requisition Tracking Number (No Value) Is the position remote? KP Onsite Is this a feeder/placement req? None of the above Is this a payroll req? No Manager Requested: Do Not Contact Yes Role Type Business Critical RPM/ClickStaff Time Entry ClickStaff Time Entry Education Bachelors Is a specific license of certification required? No Is a Motor Vehicle check required? No Is a Health Screen required? No Is a Physical Exam required? No Hours per Day 8 Hours per Week 40 Total Hours 2,080.00

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