21 Aug
|
Important Group
|
Bengaluru
21 Aug
Important Group
Bengaluru
We’re looking for a highly organized and self -driven Clinical Research Coordinator (CRC) to support clinical trial execution across partner hospitals centres. In this role, you will be responsible for end -to -end sample and patient data management, ensuring all site -level trial activities are conducted in alignment with study protocols, regulatory standards, and operational timelines.
This role requires hands -on coordination at the study site working closely with physicians, patients, and internal teams to oversee participant recruitment, informed consent, sample collection, and accurate documentation of clinical data. You’ll play a key role in implementing and maintaining study logs, ensuring equipment functionality, and facilitating timely sample shipments and record -keeping.
A core part of your responsibility will also include maintaining regulatory compliance and ensuring adherence to ICH GCP, SOPs, and institutional guidelines. You’ll act as a point of contact between the site and study teams, keeping stakeholders informed and aligned.
This is a field -facing,
people -centric role that demands clear communication, attention to detail, and a commitment to clinical quality. You’ll be encouraged to contribute proactively to process improvements and cross -site collaboration.
Requirements
- Bachelor’s degree in life sciences, nursing, pharmacy, or a related healthcare field.
- 1–3 years of experience in clinical research or patient -facing roles.
- Solid familiarity with clinical trial documentation, SOPs, and protocol workflows.
- Comfortable working in a hospital or field setting; experience handling clinical samples preferred.
- Excellent organisational skills and attention to detail.
- Strong communication and interpersonal skills, especially with physicians and patients.
- Ability to work independently, manage timelines, and follow through on operational tasks.