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Clinical Trial Feasibility/Operations Consultant - Pleasanton, United States - Abacus Service Corporation
Description
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
