Clinical Project Assistant
SanofiÂ
Advertisement
Job Description
Location: Hyderabad, Telangana, India
Job Category: Clinical Operations / Project Management
Job Type: Full-Time (On-site)
Introduction
Imaging Endpoints (IE) is a leading Imaging Technology and Clinical Research Organization (iCRO) passionately focused on our mission to Connect Imaging to the Cure™. Everything we do is driven by this vision—advancing imaging science, technology, and services to bring curative treatments to patients worldwide.
With offices in the U.S., Europe, China, and India, Imaging Endpoints is recognized as the world’s largest iCRO in oncology, supporting many of the most impactful new drug approvals.
As a Clinical Project Coordinator, you will work closely with the Operations team, study sites, and sponsors to coordinate clinical project activities. This position is ideal for individuals with strong organizational skills, an understanding of clinical research operations, and a passion for contributing to life-changing advancements in healthcare.
Role & Responsibilities
- Conduct site evaluations following standard operating procedures to determine site capability for trial participation.
- Coordinate site trainings, manage communications, and act as the primary contact for clinical trial sites.
- Maintain the Trial Master File (TMF) and ensure project documentation is complete, accurate, and compliant.
- Support audit preparation and ensure audit-readiness by maintaining study compliance documentation.
- Assist the Project Manager (PM) with project start-up activities and throughout the study lifecycle.
- Monitor project progress and update project trackers and study enrollment logs.
- Perform User Acceptance Testing (UAT) and image reconciliation as assigned.
- Track and manage incoming scans and imaging data through systems such as AG Mednet and PACS-RAW repository.
- Prepare status reports, meeting agendas, and minutes for client and internal review.
- Ensure compliance with protocol guidelines, GCP standards, and HIPAA regulations.
- Maintain confidentiality and perform other duties as assigned.
Educational Qualification
- Bachelor’s degree required (Life Sciences, Pharmacy, Biotechnology, or related field preferred).
- Clinical Research Coordinator (CRC) experience is an advantage.
- Knowledge of Good Clinical Practice (GCP), Quality Assurance, and Compliance preferred.
Â
   Experience & Skills
- Experience in the medical or clinical trials industry preferred (0–2 years).
- Strong organizational and time management skills.
- Proficiency in Microsoft Office and web-based applications.
- Excellent communication skills, both written and verbal.
- Ability to multitask, manage competing priorities, and meet deadlines.
- Detail-oriented, proactive, and able to work both independently and collaboratively.
- Commitment to confidentiality and ethical research conduct.
Location
Hyderabad, Telangana, India
Advertisement
Recent Jobs
Clinical Research Associate 1
AstraZenecaÂ
CTIS Administrator
Parexel
Clinical Research Associate (Level I, Level II & Sr. CRA)
Thermo Fisher Scientific
Associate Clinical Study Manager
Novartis
eClinical Coordinator
Medpace
Pharmacovigilance Services Associate
accenture
Associate – Regulatory Affairs
CLINCHOICE