CLINEXEL is a renowned full-service Clinical Research Organization (CRO) that specializes in providing comprehensive end-to-end services for clinical development. With a global presence spanning India, Europe, the USA, Canada, Israel, and Singapore, CLINEXEL offers clinical operations, regulatory affairs, medical writing, and pharmacovigilance solutions. We partner with pharmaceutical, biotech, and medical device companies to conduct Phase I to Phase IV clinical trials across various therapeutic areas.
As a leading CRO, we are committed to advancing medical research and improving patient outcomes by delivering high-quality, reliable clinical data. Our team is the driving force behind this commitment, and we are currently seeking motivated and experienced professionals to join our growing organization.
Responsibilities for Available Roles
1. Clinical Operations: Project Managers (02) and Clinical Research Associates (CRAs) (02)
- Project Managers will oversee the planning, execution, and successful completion of clinical trials. They will coordinate with cross-functional teams, ensuring compliance with regulatory requirements, timelines, and budget constraints.
- Clinical Research Associates (CRAs) will monitor the progress of clinical trials, ensuring that all trial activities are conducted in compliance with clinical protocols and regulatory guidelines. CRAs will be responsible for site management, patient recruitment, and data collection.
2. Medical Writing: Medical Writers (02)
- Medical Writers will prepare and review clinical trial documentation, regulatory submission documents, and publications. They will work closely with the clinical and regulatory teams to ensure clarity, precision, and adherence to scientific and regulatory standards.
Qualifications and Skills Required
For all positions, the ideal candidate should possess the following qualifications and skills:
- Clinical Operations Roles (Project Managers & CRAs):
- Bachelor’s or Master’s degree in Life Sciences, Pharmacy, or a related field.
- Proven experience in clinical trial management or monitoring.
- In-depth knowledge of GCP (Good Clinical Practice) and regulatory guidelines.
- Excellent project management skills with the ability to manage multiple tasks effectively.
- Strong communication and interpersonal skills.
- Medical Writers:
- A degree in Life Sciences, Pharmacy, Medicine, or a related field.
- Proven experience in medical writing, particularly for regulatory documents.
- Strong understanding of clinical trial processes and regulatory requirements.
- Excellent writing, editing, and proofreading skills with attention to detail.
- Ability to present complex medical data in a clear and concise manner.
How to Apply
To take the next step in your career and be part of cutting-edge clinical research, send your updated CV to careers@clinexel-cro.com.
