Research Coordinator

at  Quest Diagnostics

Birmingham, AL 35203, USA -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate22 Jul, 2024Not Specified29 Apr, 20241 year(s) or aboveMicrosoft Word,Data Collection,Outlook,Time Management,Communication Skills,Mobility,Excel,Google ProductsNoNo
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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