Clinical Project Coordinator Vacancy – Hyderabad | Imaging Endpoints

Clinical Project Coordinator Vacancy – Hyderabad | Imaging Endpoints

Imaging Endpoints hiring Clinical Project Coordinator in Hyderabad. Clinical research graduates with GCP knowledge eligible. Full-time onsite role.

Imaging Endpoints is hiring Clinical Project Coordinators for its global imaging clinical research operations in Hyderabad, Telangana. This opportunity is well suited for clinical research professionals who want to work on global oncology trials without direct patient interaction. The role offers hands-on exposure to imaging-focused clinical trials, trial master file management, audit readiness, and cross-functional project coordination within a specialized Imaging CRO (iCRO) environment.

Company Overview

Imaging Endpoints is a globally recognized Imaging Clinical Research Organization (iCRO) focused on advancing imaging science to support clinical trials, particularly in oncology. Headquartered in Scottsdale, Arizona, the organization operates across the United States, Europe, China, and India, supporting some of the most impactful new drug approvals worldwide.

As the world’s largest and most preeminent iCRO in oncology, Imaging Endpoints partners with pharmaceutical and biotechnology companies to customize imaging strategies that demonstrate therapeutic efficacy. The company is an affiliate of HonorHealth and Scottsdale Medical Imaging Limited, bringing together deep clinical expertise, imaging technology, and regulatory compliance under one global platform.

Job Role & Responsibilities

Imaging Endpoints is hiring across multiple levels within the Clinical Project Coordinator track, including Clinical Project Coordinator and Clinical Project Coordinator II. These roles closely support Project Managers, sponsors, and clinical trial sites throughout the lifecycle of imaging-based clinical studies.

Clinical Project Coordinator – Core Responsibilities

• Conduct site evaluations as per SOPs to assess readiness for imaging participation in clinical trials
• Serve as the primary point of contact for site-related clinical trial activities
• Schedule and coordinate site trainings and onboarding activities
• Own and maintain the Trial Master File (TMF) ensuring completeness, accuracy, and compliance
• Document discrepancies, define remediation plans, and coordinate corrective actions
• Support audit preparation and provide required documentation to compliance teams
• Verify processes to ensure compliance with protocol, SOPs, and regulatory requirements
• Assist Project Managers during study start-up, maintenance, and closeout phases
• Maintain and update project trackers, enrollment data, and study documentation
• Track imaging data received via CD or SFTP and upload to PACS-RAW repositories using AG Mednet
• Support CTIS-related pre-processing activities including document and data transfers
• Track and manage CRFs, queries, and clinical data flow
• Prepare clinical dossiers for reader assignments as per SSPs
• Generate weekly project status, site activity, and enrollment reports
• Schedule meetings, prepare agendas, and document meeting minutes
• Maintain confidentiality and comply with HIPAA and data privacy requirements

Clinical Project Coordinator II – Additional Responsibilities

• Collaborate closely with Project Managers on site lists, system access, and study setup
• Take ownership of audit readiness for assigned trials
• Mentor and train junior Clinical Project Coordinators
• Lead study closeout and archival activities
• Perform image reconciliation and User Acceptance Testing as assigned
• Communicate effectively with clients and internal stakeholders on project execution

These roles are critical in ensuring trial quality, regulatory compliance, and timely delivery of imaging data that supports drug development decisions.

Eligibility / Qualifications

Required Education

Candidates must hold a Bachelor’s degree in one of the following or related disciplines:
Life Sciences, Pharmacy, Biotechnology, Clinical Research, Biomedical Sciences, Allied Health Sciences

Experience Requirements

• Clinical Project Coordinator: Experience in clinical trials or healthcare operations preferred
• Clinical Project Coordinator II: Minimum 1 year of experience in clinical trials or medical research operations preferred
• Prior experience as a Clinical Research Coordinator (CRC) is an advantage

Required Knowledge & Skills

• Working knowledge of Good Clinical Practice (GCP) and clinical trial compliance
• Understanding of clinical trial documentation and Trial Master File (TMF) management
• Familiarity with CTMS, AG Mednet, imaging workflows, or PACS systems is an advantage
• Strong organizational, time management, and multitasking skills
• Excellent written and verbal communication skills
• High attention to detail and compliance-focused mindset
• Proficiency in MS Office and internet-based applications

Location & Salary

• Job Location: Hyderabad, Telangana, India
• Work Model: On-site
• Employment Type: Full-time

Application Process

Interested candidates can apply directly through the official job listing:

Apply Here: https://www.linkedin.com/jobs/view/4330557195/

Shortlisted candidates will be contacted by the Imaging Endpoints recruitment team for further evaluation.

Frequently Asked Questions (FAQs)

Is this role suitable for freshers?

Candidates with clinical research exposure or CRC experience are preferred, but healthcare experience may also be considered.

Does this role involve patient interaction?

No. This role does not involve direct patient interaction.

What therapeutic area will I work in?

Primarily oncology-focused imaging clinical trials.

Is this a CRO role?

Yes. Imaging Endpoints operates as a specialized Imaging CRO (iCRO).

What is the career growth path?

Career progression includes Senior Clinical Project Coordinator, Project Manager, and Clinical Operations leadership roles.

Job Summary Table

Company	Imaging Endpoints
Vacancies	Clinical Project Coordinator, Clinical Project Coordinator II
Required Education	Life Sciences, Pharmacy, Biotechnology, Clinical Research, Biomedical Sciences
Experience	0–2+ Years (Based on Level)

Tagged as: Pharma Jobs in Hyderabad