Bristol Myers Squibb BSc Life Sciences Clinical Trial Monitor Vacancy Available

Bristol Myers Squibb BSc Life Sciences Clinical Trial Monitor Vacancy Available

Bristol Myers Squibb BSc Life Sciences Clinical Trial Monitor Vacancy Available. BSc Life Sciences Clinical Trial Monitor Jobs. Interested and eligible applicants can check out all of the details on the same below

Hey there, looking for assistance with the possible interview questions and the answers for the role of Clinical Trial Monitor at Bristol Myers Squibb? Then check them out below

Clinical Trial Monitor

Location: Mumbai, India

Categories: Clinical Development

Req ID: R1569622

Position Type: Full Time

Posted Date: 05/23/2023

Job Description

Working with Us

Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our

work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.

BMS Hyderabad is an integrated global hub where our work is focused on helping patients prevail over serious diseases by building sustainable and innovative solutions. This important science, technology, and innovation center will support a range of technology and drug development activities that will help us usher in the next wave of innovation.

Role Summary:

Responsible for the oversight of the progress of a clinical trial, and of ensuring that it is conducted, recorded, and reported in accordance with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP). And the applicable regulatory requirements.

Key responsibilities:

• ​Act as one of the points of contact at a Site level for internal and external stakeholders.
• Identifies  new  potential  Investigators,  through  ongoing  collaborations with internal and external stakeholders.
• Assesses potential Investigators and their sites to ensure they have the resources and capabilities to conduct clinical trials.
• Develop Site relationships (incl. Contract Research Organization related issue management and non- registrational /Investigator Sponsored Research Studies)
• Recommends sites during the site feasibility and/or site selection process
• Conducts pre-study visit as appropriate
• Conducts initiation visits to ensure Investigator and site personnel receives adequate protocol specific training prior to site activation
• Reviews site activities and quality through on-site and off-site visits. Conducts monitoring activities and ensures safety and protection of study subjects as per the monitoring plan, BMS procedural documents, protocol, ICH/GCP Guidelines and other local regulations as applicable
• Perform Unblinded Site Monitor activities to protect the blind of the study by acting as secondary monitoring source separate from the blinded monitor.
• While monitoring demonstrates the ability to use data to assess risks, identify issues and make appropriate decisions.
• Serve as a point of contact for Sites
• Provides trainings to sites
• Performs site closure activities when all required protocol visits and follow-up are completed
• Manages multiple protocols, across multiple therapeutic areas, which may require travel, based upon assigned site location and/or geographic territory.
• Ensures completeness and quality of data submitted from study sites. Ensures eCRF data is available and current by using the available systems to follow site activities.
• Oversees activities of site personnel over whom there is no direct authority.
• Motivates/influences the site to meet study objectives, including enrolment and retention goals. Demonstrates flexibility and adaptability when communicating with different stakeholders utilizing the most appropriate communication method
• Anticipates, identifies and proactively supports site in resolving issues as they occur. Appropriately documents and promptly escalates serious or persistent outstanding issues to management and project team. Initiates, recommends, documents and communicates corrective actions as needed and follows up to ensure corrective/preventive actions based on root cause analysis are implemented
• Involvement in Regulatory Compliance audit/inspection process, as needed. This includes the development and implementation of site corrective and preventive actions
• Prepares and submits written reports, both monitoring and administrative, in a timely, accurate, concise, professional and objective manner
• Support Ethics Committee submission, ICF review, collection of documents to/from site
• Support ensuring access to eDC and BMS / vendor systems is available for clinical trial site personnel
• Support equipment calibration and tracking
• Support preparation of Study Initiation Visit materials
• Support coordination and ensure database lock timelines are met as required locally

Degree/Certification/Licensure:

• Bachelor’s degree required preferably within life sciences or equivalent

Experience – Responsibility and minimum number of years

• Clinical Trial Monitor:   3-4years of relevant clinical research experience, able to work independently.
• Relevant prior Pharma/Biotech Sponsor employment or experience as a clinical study coordinator preferred
• Experience in the drug discovery/development process.

Competencies – knowledge, skills, abilities, other

• Has basic to good knowledge of ICH/GCP Guidelines and applicable local laws and regulations (Health Authorities) which govern clinical trials.
• Knowledge and understanding of clinical research processes, regulations and methodology
• Understands clinical landscape with practical knowledge of a variety of medical settings and medical records management
• Organization and time management skills
• Ability to build, maintain and strengthen relationships even under pressure and/ or in difficult situations
• Good verbal and written communication skills (both in English and local language).

Software that must be used independently and without assistance

• Microsoft Suite
• Clinical Trial Management Systems (CTMS)
• Electronic Data Capture Systems (eDC)
• Electronic Trial Master File (eTMF)
• Metrics websites

#HYDDD

If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Uniquely Interesting Work, Life-changing Careers

With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol

Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [email protected]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

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Hey there, looking for assistance with the possible interview questions and the answers for the role of Clinical Trial Monitor at Bristol Myers Squibb? Then check them out below

1. Can you explain your experience and knowledge of Good Clinical Practice (GCP) guidelines and applicable regulations in clinical trials? Answer: I have a solid understanding of GCP guidelines and the local laws and regulations that govern clinical trials. I have actively applied this knowledge in my previous roles as a Clinical Trial Monitor, ensuring that trials are conducted in compliance with these guidelines and regulations. I am familiar with documentation requirements, ethics committee submissions, and the overall clinical research process.
2. How do you assess potential investigators and their sites to ensure they have the necessary resources and capabilities to conduct clinical trials? Answer: When assessing potential investigators and sites, I focus on evaluating their capabilities, resources, and previous experience in conducting clinical trials. I conduct thorough site feasibility assessments, including reviewing their track record, infrastructure, and personnel qualifications. I also collaborate with internal and external stakeholders to gather insights and recommendations on potential investigators.
3. Can you discuss your experience in conducting monitoring activities and ensuring the safety and protection of study subjects? Answer: Monitoring activities are crucial to ensuring the integrity and quality of clinical trials. In my previous roles, I have conducted both on-site and off-site visits to review site activities, data completeness, and adherence to protocol, ICH/GCP guidelines, and local regulations. I am experienced in identifying risks, assessing issues, and making informed decisions to protect the safety and well-being of study subjects.
4. How have you managed multiple protocols across different therapeutic areas while meeting enrollment and retention goals? Answer: Managing multiple protocols requires effective organization, prioritization, and communication skills. I have successfully handled diverse therapeutic areas and coordinated with different study teams to meet enrollment and retention goals. I ensure clear and timely communication with sites, motivate and influence site personnel, and proactively address any issues or challenges that may arise during the course of the trials.
5. Can you explain your experience with clinical trial management systems (CTMS), electronic data capture systems (eDC), and electronic trial master file (eTMF)? Answer: I have hands-on experience with various clinical trial management systems, electronic data capture systems, and electronic trial master file systems. I am proficient in using these tools to track and manage study activities, monitor data quality, and maintain accurate and up-to-date documentation. I have utilized CTMS for study planning and oversight, eDC for data entry and validation, and eTMF for document management in compliance with regulatory requirements.

Editor’s Note: Bristol Myers Squibb BSc Life Sciences Clinical Trial Monitor Vacancy Available. Bristol Myers Squibb BSc Jobs. Bristol Myers Squibb BSc Vacancies. Please ensure you are subscribed to the Biotecnika Times Newsletter and our YouTube channel to be notified of the latest industry news. Follow us on social media like Twitter, Telegram, Facebook and Instagram.