Research Coordinator
at Quest Diagnostics
Birmingham, AL 35203, USA -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 22 Jul, 2024 | Not Specified | 29 Apr, 2024 | 1 year(s) or above | Microsoft Word,Data Collection,Outlook,Time Management,Communication Skills,Mobility,Excel,Google Products | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
PREFERRED WORK EXPERIENCE:
- Experience with research coordination
- Experience contributing to formative research processes (e.g., literature reviews, interviews)
PHYSICAL AND MENTAL REQUIREMENTS:
- Ability to read small print.
- Requires mobility of arms to reach and dexterity of hands to grasp and manipulate small objects.
- Performs lifting, pushing and/or pulling which does not exceed 25 pounds and is an infrequent aspect of the job.
Knowledge:
- Working knowledge of Microsoft Word, Excel, Google Products, and Outlook
Skills:
- Exceptional communication skills both written and oral.
- Ability to stay organized and manage multiple projects / relationships simultaneously.
- Strong time management and the ability to work independently with minimal oversight.
- Exceptional analytical and problem-solving skills. Ability to distill down complicated data.
- Ability to work as a team, be coachable, and collaborate with key stakeholders across different functions.
Responsibilities:
Responsibilities:
- Coordinates patient care and/or patient follow-up functions of the clinical study including planning and developing related activities
- Employs strategies to maintain recruitment and retention rates
- Participate in research education and training activities
- Recruits, schedules, and performs follow-up with research subjects
- Maintains current contact information for all study participants and has good interviewing and communication skills
- Assists with qualitative and quantitative data collection
- Escalates adverse events (AEs) if and as required by the protocol and research agreements
- Compiles, edits, and proofs written reports for both internal and external administrative offices
- Assists with development of standard operating procedures (SOPs) for data quality assurance
- Achieves and maintains human subjects and good clinical practice training
- Maintains compliance with federal, state and accrediting agencies (sponsors) as require
REQUIREMENT SUMMARY
Min:1.0Max:3.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
Birmingham, AL 35203, USA