
Clinical Research Professional
5 days ago
Job Description:
As a fresher clinical research executive, you will be responsible for creating and writing trial protocols, presenting them to the steering committee, and identifying, evaluating, and establishing trial sites. You will also oversee site staff training on therapeutic areas, protocol requirements, source documentation, and case report form completion.
Your duties will include liaising with ethics committees regarding the rights, safety, and well-being of trial subjects. You will also order, track, and manage IP and trial materials, overseeing and documenting IP dispensing, inventory, and reconciliation.
In addition, you will protect subjects' confidentiality, update their information, and verify that IP has been dispensed and administered according to protocol. Conducting regular site visits, coordinating project meetings, and writing visit reports are also part of your responsibilities.
This role requires strong analytical and problem-solving skills, attention to detail, and excellent communication and interpersonal skills. If you are passionate about advancing medical research and working in a dynamic environment, we encourage you to apply.
Key Skills and Qualifications:
* Strong understanding of clinical trials and regulatory requirements
* Excellent communication and interpersonal skills
* Ability to work independently and as part of a team
* Strong analytical and problem-solving skills
* Attention to detail and ability to maintain accurate records
Benefits:
* Opportunity to work in a dynamic and growing industry
* Chance to develop your career in clinical research
* Collaborative and supportive work environment
Others:
* This is an entry-level position suitable for recent graduates or those looking to transition into a career in clinical research.
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