Clinical Trial Associate
4.
7 Raritan, NJ Raritan, NJ Full-time Full-time $65,000 - $68,000 a year $65,000 - $68,000 a year 23 hours ago 23 hours ago 23 hours ago Our Client, a major medical devices company (a subsidiary of a major pharmaceutical and healthcare products company) is seeking several experienced research professionals for its medical devices group.
The position is responsible for providing project management coordination and the timely tracking of study essential documents and ensuring completeness of the Trial Master File for assigned clinical studies.
You Must reside in the Boston, MA; Philadelphia, PA; Warsaw, IN; Cincinnati, OH market areas to be considered.
Candidates Are Not Required to Have Medical Device Experience.
Positions offer excellent compensation and benefits, paid vacation, 401K, sick and personal time and much more.
These are full-time (W2) employee positions with excellent career growth.
If you have a solid understanding of clinical research processes, GCPs, and an understanding of regulations and standards.
we want to hear from you.
Education A Bachelor Degree or Direct experience is required.
Basic Job Description Accountable for the timely tracking of study essential documents and ensuring completeness of the Trial Master File for assigned clinical studies.
Assisting study staff and investigators to effectively resolve issues relating to Study Files (Trial Master File and Investigator Site File).
Responding to problems and assisting in implementing corrective and preventive actions Tracking of study activities (site visits, contracts, submissions, safety, communication etc.
) and documents relating to such activities.
Demonstrated competencies in the following areas are required:
Solid Teamwork Skills Excellent Written and Verbal Communications Ability to Present to Small Groups Strong organizational skills (e.
g.
, able to manage multiple sub-projects and tasks simultaneously and consistently meet all associated deadlines).
Attention to detail PRI is an equal opportunity employer Job Type:
Full-time Pay:
$65,000.
00 - $68,000.
00 per year
Benefits:
401(k) 401(k) matching Dental insurance Flexible spending account Health insurance Life insurance Paid time off Referral program Retirement plan Vision insurance Schedule:
8 hour shift Application Question(s):
This position will require in-office work from office in one of the following locations:
Raynahm, MA or West Chester, PA or Warsaw, IN or Cincinnati, OH.
Do you live in one of these markets? Education:
Bachelor's (Required)
Experience:
Clinical research:
2 years (Required) Ability to Commute:
Raritan, NJ (Required) Work Location:
In person Demonstrated competencies in the following areas are required:
.
Estimated Salary: $20 to $28 per hour based on qualifications.
7 Raritan, NJ Raritan, NJ Full-time Full-time $65,000 - $68,000 a year $65,000 - $68,000 a year 23 hours ago 23 hours ago 23 hours ago Our Client, a major medical devices company (a subsidiary of a major pharmaceutical and healthcare products company) is seeking several experienced research professionals for its medical devices group.
The position is responsible for providing project management coordination and the timely tracking of study essential documents and ensuring completeness of the Trial Master File for assigned clinical studies.
You Must reside in the Boston, MA; Philadelphia, PA; Warsaw, IN; Cincinnati, OH market areas to be considered.
Candidates Are Not Required to Have Medical Device Experience.
Positions offer excellent compensation and benefits, paid vacation, 401K, sick and personal time and much more.
These are full-time (W2) employee positions with excellent career growth.
If you have a solid understanding of clinical research processes, GCPs, and an understanding of regulations and standards.
we want to hear from you.
Education A Bachelor Degree or Direct experience is required.
Basic Job Description Accountable for the timely tracking of study essential documents and ensuring completeness of the Trial Master File for assigned clinical studies.
Assisting study staff and investigators to effectively resolve issues relating to Study Files (Trial Master File and Investigator Site File).
Responding to problems and assisting in implementing corrective and preventive actions Tracking of study activities (site visits, contracts, submissions, safety, communication etc.
) and documents relating to such activities.
Demonstrated competencies in the following areas are required:
Solid Teamwork Skills Excellent Written and Verbal Communications Ability to Present to Small Groups Strong organizational skills (e.
g.
, able to manage multiple sub-projects and tasks simultaneously and consistently meet all associated deadlines).
Attention to detail PRI is an equal opportunity employer Job Type:
Full-time Pay:
$65,000.
00 - $68,000.
00 per year
Benefits:
401(k) 401(k) matching Dental insurance Flexible spending account Health insurance Life insurance Paid time off Referral program Retirement plan Vision insurance Schedule:
8 hour shift Application Question(s):
This position will require in-office work from office in one of the following locations:
Raynahm, MA or West Chester, PA or Warsaw, IN or Cincinnati, OH.
Do you live in one of these markets? Education:
Bachelor's (Required)
Experience:
Clinical research:
2 years (Required) Ability to Commute:
Raritan, NJ (Required) Work Location:
In person Demonstrated competencies in the following areas are required:
.
Estimated Salary: $20 to $28 per hour based on qualifications.
|
|
 | |
