Clinical Research Associate
4 days ago
We are seeking a highly skilled Clinical Research Associate to join our team in the pharmaceutical industry. As a Clinical Research Associate, you will be responsible for monitoring and managing clinical trials, ensuring compliance with regulatory requirements and Good Clinical Practice guidelines.
Key Responsibilities- Monitor and manage clinical trials, including site initiation, interim monitoring, and close-out visits.
- Ensure compliance with regulatory requirements and Good Clinical Practice guidelines.
- Develop and maintain site start-up documents, including SIV agendas.
- Provide training and support to site staff on study protocols and procedures.
- Represent the company at site meetings and communicate with site staff as needed.
- Conduct risk-based monitoring and identify potential issues that may impact the trial.
- Collaborate with cross-functional teams to ensure trial success.
- Bachelor's degree in a life science or related field.
- Minimum 2 years of experience in clinical research, preferably in the pharmaceutical industry.
- Knowledge of Good Clinical Practice guidelines and regulatory requirements.
- Excellent communication and interpersonal skills.
- Ability to work independently and as part of a team.
- Strong analytical and problem-solving skills.
We offer a competitive salary and benefits package, including health insurance, retirement planning, and flexible work arrangements. Our company values diversity, inclusion, and belonging, and we are committed to creating a workplace that is free from discrimination and harassment.
Apply now to join our team and contribute to the success of our clinical trials.
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