Clinical Research Associate @ Techno Endura

Job Description

Responsibilities:

• Pre-Trial:
  • Identify and qualify potential clinical trial sites and investigators.
  • Set up and equip trial sites with necessary materials and equipment.
  • Train site staff on study procedures and data collection methods.
  • Develop and maintain study manuals and documentation.
• Monitoring:
  • Conduct regular visits to trial sites to monitor progress and adherence to protocols.
  • Review case report forms and other data for accuracy and completeness.
  • Identify and address any safety concerns or protocol deviations.
  • Report significant findings and updates to sponsors and regulatory authorities.
• Post-Trial:
  • Assist with data analysis and study close-out activities.
  • Prepare final study reports and presentations.
  • Contribute to the regulatory submission process.

Additional responsibilities may include:

• Managing study budgets and timelines.
• Liaising with ethics committees and regulatory agencies.
• Providing scientific and technical support to study teams.
• Participating in training and development programs.

Qualifications:

• 0- 2 years' experience 
• Bachelor's degree in life sciences, nursing, or a related field.
• Master's degree preferred, especially for senior positions.
• Good understanding of Good Clinical Practice guidelines and regulations.
• Excellent communication, interpersonal, and organizational skills.
• Strong attention to detail and ability to multitask.
• Ability to travel frequently and independently.

Interested to apply can share Cv or call/WhatsApp to hidden_mobile 
 

Employement Category:

Employement Type: Full time
Industry: Medical / Healthcare
Role Category: Pharmacist / Medical Representative
Functional Area: Not Applicable
Role/Responsibilies: Clinical Research Associate

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Keyskills:   clinical practices clinical monitoring scientific analysis clinical research clinical trials clinical data management