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IQVIA BSc Trainee Job For Life Sciences, Apply Online
IQVIA BSc Trainee Job For Life Sciences, Apply Online. IQVIA Bengaluru BSc Life Sciences Safety Associate Trainee job opening. BSc Life Sciences Jobs. Interested and eligible applicants can check out all of the details on the same below
If are you looking for some interview questions for the Safety Associate Trainee at IQVIA, then check the bottom of the page.
Name of the Post – Safety Associate Trainee
Primary Location: Bangalore, India
Req ID – R1306020
Job Description Summary
Job Overview
Review, assess and process Safety data and information, across service lines, received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations Standard Operating Procedures (SOPs) and internal guidelines under guidance and support of senior operation team members.
Essential Functions
- To Prioritize and complete the assigned trainings on time.
- Process Safety data according to applicable regulations, guidelines, Standard Operating procedures (SOPs) and project requirements.
- To perform Pharmacovigilance activities per project requirement including but not limited to, collecting and tracking incoming – Adverse Events(AE)/endpoint information
- determining initial/update status of incoming events
- database entry
- coding AE and Products, writing narratives, Literature related activities as per internal/ project timelines.
- Ensure to meet quality standards per project requirements.
- Ensure to meet productivity and delivery standards per project requirements.
- To ensure compliance to all project related processes and activities.
- Read and acknowledge all necessary IQVIA standard operating procedures (SOPs) and customer SOPs as required. Ensure all required training is executed in a timely fashion and documented. Work towards ensuring your individual training plan and training transcript are reconcilable.
- Creating, maintaining and tracking cases as applicable to the project plan.
- Identify quality problems, if any, and bring them to the attention of a senior team member.
- To demonstrate problem solving capabilities.
- Liaise with different functional team members, e.g. project management, clinical, data management
- health care professionals e.g. investigators, medical monitors, site coordinators and designees to address project related issues.
- May liaise with client in relation to details on day to day case processing activities.
- To mentor new teams members, if assigned by the Manager.
- Attend project team meetings and provide feedback to operations manager on any challenges/issues or successes.
- Perform other duties as assigned.
- Lead/ Support department Initiatives
- 100% compliance towards all people practices and processes
Qualifications
- High School Diploma or equivalent Scientific or healthcare discipline or allied life sciences Req
- Bachelor’s degree in life sciences or related field and up to 3 years of relevant experience, inclusive of up to 1 year of Pharmacovigilance experience.
- r equivalent combination of education, training and experience.
- Good knowledge of medical terminology.
- Working knowledge of applicable Safety Database and any other internal/Client applications.
- Knowledge of applicable global, regional, local clinical research regulatory requirements.
- Excellent attention to detail and accuracy.
- maintain high quality standards.
- Good working knowledge of Microsoft Office and web-based applications.
- Strong organizational skills and time management skills.
- Strong verbal/written communication skills.
- Self-motivated and flexible.
- Ability to follow instructions/guidelines, utilize initiative and work independently.
- Ability to multi-task, meet strict deadlines, manage competing priorities and changing demands.
- Ability to delegate to less experienced team members.
- Ability to be flexible and receptive to changing process demands.
- Willingness and aptitude to learn new skills across Safety service lines.
- Ability to establish and maintain effective communication and working relationships with coworkers, managers and clients.
- Ability to work as a Team Player, contribute and work towards achieving Team goals.
- Ensure quality of deliverables according to the agreed terms.
- Demonstration of IQVIA core values while doing daily tasks – Extensive use of keyboard requiring repetitive motion of fingers.
- Extensive use of telephone and face-to-face communication requiring accurate perception of speech.
- Regular sitting for extended periods of time.
- May require occasional travel.
- Flexibility to operate in shifts.
If you are looking for some interview questions for the role of Safety Associate Trainee only at IQVIA then check them out below
- Can you explain the process of reviewing and processing safety data in compliance with applicable regulations and SOPs?
- Answer: As a Safety Associate Trainee, I would review and assess safety data received from various sources and process it according to regulations, guidelines, and project requirements. This includes activities such as collecting and tracking adverse events, determining the status of incoming events, database entry, coding AE and products, writing narratives, and performing literature-related activities within the specified timelines.
- How do you ensure compliance with quality standards and productivity requirements in your work?
- Answer: I prioritize quality by paying close attention to detail and accuracy. I follow the applicable SOPs and guidelines, maintain a good knowledge of medical terminology, and utilize the safety database and other necessary applications effectively. Time management skills and organizational abilities help me meet productivity and delivery standards, ensuring compliance with project requirements.
- Can you describe your experience in pharmacovigilance and your familiarity with global, regional, and local clinical research regulatory requirements?
- Answer: With up to 1 year of pharmacovigilance experience and a strong academic background in life sciences, I have gained knowledge of pharmacovigilance principles and practices. I am familiar with global, regional, and local clinical research regulatory requirements, which enables me to perform my duties in accordance with these regulations.
- How do you handle challenging situations and problem-solving in the context of safety data processing?
- Answer: When faced with challenges, I approach problem-solving systematically. I utilize my knowledge and experience, seek guidance from senior team members when needed, and effectively communicate with relevant stakeholders such as project management, clinical teams, and healthcare professionals. I am adaptable, flexible, and willing to learn new skills to address changing process demands.
- How do you demonstrate effective communication and teamwork in your role as a Safety Associate Trainee?
- Answer: Communication and teamwork are essential in my role. I maintain strong verbal and written communication skills, enabling me to collaborate effectively with coworkers, managers, and clients. I actively contribute to team goals, delegate tasks when appropriate, and establish and maintain positive working relationships. I am receptive to feedback, demonstrate a willingness to learn, and uphold IQVIA’s core values in my daily tasks.
Note: The answers provided here are general examples and should be tailored to your own experiences and knowledge during the interview.
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