Document Coordinator, Global Trial Acceleration
Welcome to Bristol-Myers Squibb, a global biopharmaceutical company dedicated to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. We are currently seeking a highly motivated and detail-oriented Document Coordinator to join our Global Trial Acceleration team. In this role, you will play a critical part in supporting the execution of clinical trials, ensuring the accuracy and completeness of all trial-related documents. If you are a self-starter with strong organizational skills and a passion for making a meaningful impact in the healthcare industry, we encourage you to apply. Join us in our mission to transform patients' lives through science and innovation.
- Maintain and organize all trial-related documents, including study protocols, informed consent forms, and regulatory submissions.
- Ensure the accuracy and completeness of all trial documents by conducting thorough quality checks and following proper document control processes.
- Collaborate with cross-functional teams to gather and compile necessary documents for trial initiation, conduct, and close-out.
- Maintain electronic document management systems and assist with the development and implementation of document management procedures.
- Track and report on document status and progress to ensure timely completion and submission.
- Communicate with internal and external stakeholders to ensure timely and accurate document exchange.
- Serve as a point of contact for document-related inquiries and provide support to the study team as needed.
- Assist with the preparation and formatting of documents for submission to regulatory authorities.
- Adhere to company and industry regulations, policies, and procedures related to document management.
- Continuously evaluate and improve document management processes to increase efficiency and accuracy.
- Stay up-to-date with industry trends and best practices in document management.
- Participate in team meetings and trainings to ensure alignment and consistency across trials.
- Contribute to a positive and collaborative work environment by fostering open communication and teamwork.
Bachelor's Degree In A Relevant Field Such As Business Administration, Project Management, Or Life Sciences.
Minimum Of 3 Years Of Experience In Document Coordination Or Project Management In A Clinical Trial Environment.
Familiarity With Regulatory Requirements And Guidelines For Clinical Trial Documentation, Such As Ich-Gcp And Fda Regulations.
Excellent Organizational And Time Management Skills, With The Ability To Prioritize Tasks And Manage Multiple Projects Simultaneously.
Strong Communication And Interpersonal Skills, With The Ability To Collaborate With Cross-Functional Teams And External Partners In A Global Setting.
Quality Assurance
Communication Skills
Project Planning
Data Analysis
Time Management
Attention to detail
Document management
Teamwork
Regulatory compliance
Cross-Functional Collaboration
Trial Coordination
Communication
Conflict Resolution
Customer Service
Emotional Intelligence
Leadership
Time management
creativity
Teamwork
Adaptability
Problem-Solving
According to JobzMall, the average salary range for a Document Coordinator, Global Trial Acceleration in Hyderabad, Telangana, India is between ₹4,00,000 - ₹6,00,000 per year. This range can vary depending on factors such as the company, level of experience, and specific job responsibilities.
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Bristol-Myers Squibb Co. operates as a biopharmaceutical company, which engages in the discovery, development, licensing, manufacturing, marketing, distribution, and sale of biopharmaceutical products. It includes chemically-synthesized drugs or small molecules and products produced from biological processes called biologics.
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