Imaging Endpoints is inviting applications for the position of Clinical Project Coordinator in Hyderabad, Telangana. This is an excellent opportunity for candidates interested in clinical research, clinical trial operations, clinical project management, and imaging-based clinical trials.

The company is one of the world’s leading Imaging Contract Research Organizations (iCROs) specializing in oncology clinical trials. Professionals with knowledge of Good Clinical Practice (GCP), clinical documentation, and clinical operations are encouraged to apply.

If you are looking for Clinical Project Coordinator jobs in Hyderabad, clinical research jobs for life science graduates, or clinical trials jobs in India, this opportunity offers excellent career growth in a global clinical research organization.

Job Details

About Imaging Endpoints

Imaging Endpoints (IE) is a globally recognized Imaging Clinical Research Organization (iCRO) focused on advancing imaging science to accelerate drug development, particularly in oncology. The company collaborates with pharmaceutical sponsors, research institutions, and healthcare organizations worldwide to support imaging-based clinical trials.

With offices across the United States, Europe, India, and China, Imaging Endpoints has contributed to numerous oncology drug approvals by providing innovative imaging solutions for clinical research.

Key Responsibilities

Selected candidates will be responsible for:

• Coordinate clinical project activities with sponsors and research sites.
• Conduct site capability evaluations according to SOPs.
• Schedule and organize site initiation and training sessions.
• Act as the primary contact for assigned clinical trial sites.
• Maintain Trial Master File (TMF) documentation.
• Ensure study documents remain audit-ready.
• Support project startup and study lifecycle activities.
• Track study enrollment and project milestones.
• Manage Case Report Forms (CRFs), clinical queries, and data flow.
• Upload imaging scans using AG Mednet and PACS repositories.
• Assist with CTIS preprocessing activities.
• Generate project status, enrollment, and site reports.
• Coordinate meetings, prepare agendas, and document meeting minutes.
• Support User Acceptance Testing (UAT).
• Ensure compliance with GCP, SOPs, HIPAA, and regulatory requirements.
• Communicate with study sites regarding pending documentation and queries.
• Assist Project Managers in achieving study timelines.

Educational Qualification

Candidates should possess:

• Bachelor’s degree in:
  • Life Sciences
  • Pharmacy
  • Biotechnology
  • Biomedical Sciences
  • Nursing
  • Medical Sciences
  • Clinical Research
  • Or other related healthcare disciplines

Experience Required

Clinical Project Coordinator

• Freshers with relevant clinical research exposure may be considered.
• Experience in healthcare or clinical research is an added advantage.
• Prior experience as a Clinical Research Coordinator (CRC) is preferred.

Clinical Project Coordinator II

• Minimum 1 year of experience in clinical research or clinical trials.
• Experience in clinical operations or site coordination preferred.

Required Skills

Applicants should have:

• Good Clinical Practice (GCP) knowledge
• Clinical trial documentation
• Trial Master File (TMF) management
• Case Report Form (CRF) handling
• Clinical Operations knowledge
• Excellent communication skills
• Strong organizational abilities
• Time management
• MS Office proficiency
• Attention to detail
• Team collaboration
• Problem-solving skills
• Regulatory compliance understanding
• Ability to multitask under deadlines

Preferred Qualifications

Candidates with any of the following will have an advantage:

• Clinical Research Coordinator (CRC) experience
• Clinical operations experience
• Imaging clinical trial exposure
• Quality Assurance or Compliance knowledge
• Oncology clinical trial experience

Why Join Imaging Endpoints?

Employees can expect:

• Opportunity to work with a globally recognized Imaging CRO.
• Exposure to international oncology clinical trials.
• Career development in clinical research operations.
• Collaborative and highly skilled global teams.
• Learning opportunities in imaging technologies.
• Stable full-time employment.
• Professional growth within clinical project management.

Salary (Expected)

Based on current industry standards for similar roles in Hyderabad:

Estimated Salary: ₹4.8 LPA – ₹7.5 LPA

(Actual compensation depends on qualifications, experience, and interview performance.)

Work Location

Hyderabad, Telangana, India

Work Mode: On-site

How to Apply

Application Link