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Central Study Coordinator

3+ years
Not Disclosed
10 Jan. 3, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Central Study Coordinator
Company: ProPharma Group
Location: Remote
Position Type: Full-Time


About ProPharma Group

For over 20 years, ProPharma has been improving patient health and wellness by empowering biotech, pharmaceutical, and medical device organizations to advance scientific breakthroughs and bring new therapies to market. As the world’s largest Research Consulting Organization (RCO), ProPharma offers an end-to-end suite of customizable solutions, leveraging deep expertise in regulatory sciences, clinical research, quality & compliance, pharmacovigilance, and more.


Position Overview

ProPharma is seeking a Central Study Coordinator to join the clinical monitoring team. This role is responsible for overseeing clinical studies, ensuring they are conducted according to protocol, regulatory guidelines, and GCP standards. The Central Study Coordinator will work closely with study teams and investigational sites to ensure smooth and compliant study execution.


Key Responsibilities

  • Clinical Monitoring & Study Oversight:
    • Monitor clinical trials for assigned protocols and investigational sites.
    • Ensure studies are conducted in accordance with the study protocol, GCP, and regulatory requirements.
    • Assist with study documentation and site management as needed.
  • Collaboration & Teamwork:
    • Work independently and collaborate effectively with Research Associates (RAs) and Clinical Study Coordinators (CSCs) to complete delegated tasks.
  • Communication:
    • Communicate effectively with the study team and stakeholders regarding study progress, issues, and resolutions.
  • Technology Management:
    • Manage web-based research platforms and technology tools on PC (Microsoft OS) for remote work.

Minimum Qualifications

  • Research Experience: Previous research experience is preferred.
  • Technology Skills: Ability to manage technology and web-based research platforms on a PC (Microsoft OS).
  • Team Experience: Previous experience working as part of a study team is ideal.
  • Critical Thinking: Strong problem-solving and analytical skills.
  • Communication: Strong verbal and written communication skills.
  • Independent & Collaborative Work: Ability to work both independently and collaboratively with a team.
  • Privacy: Ability to maintain privacy in the work environment.

Additional Information:

  • ProPharma is committed to diversity, equity, and inclusion and creates an environment where all employees can be their authentic selves and feel empowered to succeed.
  • #LI-Remote
  • ProPharma does not accept unsolicited resumes from recruiters or third parties.

How to Apply:

Interested candidates should apply directly through ProPharma’s career portal.


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