Job Description

Responsibilities

• Develop and maintain study protocols and case report forms.
• Recruit and screen study participants per study criteria.
• Obtain informed consent from study participants and explain study procedures.
• Collect and manage study data, including adverse events and other safety-related information.
• Monitor study participant compliance and follow-up visits.
• Manage study supplies, equipment, and inventory.
• Assist with preparing and submitting study-related documentation to regulatory agencies and institutional review boards.
• Collaborate with study sponsors and principal investigators to ensure that studies are conducted according to protocol.
• Communicate study progress to research staff and other stakeholders.
• Ensure that study data is collected and managed in accordance with regulatory requirements and study protocol.

Requirements

• Bachelor's degree in a scientific or healthcare-related field
• Strong organizational and project management skills
• Excellent attention to detail and accuracy
• Strong communication and interpersonal skills
• Ability to work well under pressure and within strict timelines
• Knowledge of clinical research protocols, case report forms, and study procedures
• Proficiency in Microsoft Office and other relevant software applications

Job Types: Full-time, Permanent, Fresher

Pay: ?30,721.80 - ?45,900.04 per month

Benefits:

• Health insurance
• Provident Fund

Schedule:

• Day shift

Supplemental Pay:

• Performance bonus
• Yearly bonus

Experience:

• total work: 1 year (Preferred)

Work Location: In person