The field of clinical research is the backbone of modern medicine. It is where scientific hypothesis meets patient care to create life-saving treatments. Global MedTrial, a growing clinical research organization, is expanding its specialized team in Pune, Maharashtra and is currently hiring a Clinical Research Coordinator (CRC) for upcoming Respiratory Clinical Trials.
If you have experience managing clinical trial site activities and are passionate about patient safety, regulatory compliance, and accurate clinical data management, this opportunity could be the next step in your clinical research career.
🧪 Role Overview: Clinical Research Coordinator (CRC)
A Clinical Research Coordinator (CRC) plays a central role in the successful execution of clinical trials. At Global MedTrial, the CRC acts as the key link between investigators, trial participants, and pharmaceutical sponsors.
This role goes beyond administrative work—you will ensure that every clinical trial activity follows strict scientific and ethical standards.
Key Responsibilities
1. Protocol Management
- Ensure all trial procedures follow sponsor protocols and regulatory requirements.
- Maintain accurate documentation and compliance throughout the study lifecycle.
2. Patient Interaction
- Screen and recruit eligible patients for respiratory studies.
- Obtain informed consent and guide participants through trial procedures.
3. Data Integrity & Documentation
- Maintain Case Report Forms (CRFs) and ensure accurate source documentation.
- Ensure all trial data is complete, accurate, and audit-ready.
4. Site Coordination
- Manage investigational medicinal products (IMPs).
- Coordinate laboratory samples and trial logistics.
5. Regulatory Compliance
- Ensure all activities follow ICH-GCP (Good Clinical Practice) guidelines and local regulatory standards.
🫁 Specialization: Respiratory Clinical Trials
Global MedTrial is specifically looking for professionals with experience in respiratory trials.
Respiratory research plays a crucial role in improving treatments for conditions such as:
- Asthma
- Chronic Obstructive Pulmonary Disease (COPD)
- Pulmonary infections
- Emerging respiratory diseases
Why Respiratory Trial Experience Matters
Respiratory clinical trials require specialized knowledge of:
- Pulmonary Function Tests (PFTs)
- Spirometry procedures
- Patient monitoring for respiratory conditions
- Handling respiratory trial endpoints and safety assessments
Your expertise in these areas helps ensure both patient safety and reliable clinical data.
📍 Location: Pune (On-Site Role)
This position is based in Pune, one of India’s rapidly growing hubs for pharmaceutical research, clinical trials, and biotechnology companies.
Work Environment
- On-site role for direct patient interaction and site coordination
- Collaborative work culture with investigators and clinical teams
- Opportunity to work on globally aligned clinical trials
The company is currently prioritizing immediate joiners, making it an excellent opportunity for professionals ready to transition quickly.
📝 Eligibility Criteria
Candidates interested in applying should meet the following requirements:
- Experience as a Clinical Research Coordinator (CRC)
- Prior exposure to Respiratory Clinical Trials
- Strong knowledge of CRO/SMO workflows
- Understanding of ICH-GCP guidelines and clinical trial regulations
- Ability to communicate complex medical procedures to patients clearly
- Experience using Electronic Data Capture (EDC) systems and clinical trial software
✨ Benefits of Joining Global MedTrial
Working with Global MedTrial offers several professional advantages:
- Exposure to international clinical trial standards
- Opportunity to work with advanced medical research technologies
- Strong career growth in clinical research
- Contribution to meaningful healthcare innovation
Every study coordinated contributes to developing better respiratory treatments for patients worldwide.
📧 How to Apply
Interested candidates can apply by sending their updated CV.
Email: hr@globalmedtrial.com
Suggested Subject Line:
Application for CRC – Respiratory Trials – [Years of Experience] – [Your Name]
