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hace 2 meses
We are seeking a highly skilled and detail-oriented individual to join our team as a Clinical Research Associate. In this role, you will be responsible for managing clinical trials, conducting site visits, and ensuring compliance with regulatory requirements.
Key Responsibilities- Manage clinical trials from initiation to close-out, ensuring timely and efficient execution
- Conduct site visits to monitor trial progress, identify issues, and implement corrective actions
- Ensure compliance with ICH GCPs, regulatory requirements, and company policies
- Develop and maintain strong relationships with site personnel, investigators, and other stakeholders
- Collaborate with cross-functional teams to resolve issues and improve trial performance
- Bachelor's degree in a life sciences related field or equivalent experience
- Minimum 2 years of clinical research experience, preferably in a clinical trials environment
- Strong knowledge of medical terminology, anatomy, and ICH GCPs
- Excellent communication, interpersonal, and organizational skills
- Ability to work independently and as part of a team
This role requires frequent travel, approximately 60-80% of the time, with occasional overnight stays. You will be exposed to biological fluids and may be required to wear personal protective equipment. The work environment is typically office/ laboratory/clinical/and/or home office setting with exposure to electrical office equipment.
Physical Requirements- Ability to work in an upright and/or stationary position for 6-8 hours per day
- Repetitive hand movement and frequent mobility required
- Occasional crouching, stooping, and light to moderate lifting (up to 15-20 lbs)
We offer a competitive salary and benefits package, as well as opportunities for professional growth and development. If you are a motivated and detail-oriented individual with a passion for clinical research, we encourage you to apply for this exciting opportunity.