IQVIA BSc Vacancies Freshers – Life Sciences Candidates Apply
IQVIA BSc Vacancies Freshers – Life Sciences Candidates Apply. 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 Lab Project Svcs Coord at IQVIA, then check the bottom of the page.
Name of the Post – Lab Project Svcs Coord
Primary Location: Bangalore, India
Req ID – R1351680
Job Overview
Provide support to the Project Manager and related team members by performing routine procedures and tasks associated with the day to day running of projects throughout the entire study lifecycle (e.g. start-up, maintenance and close-out). Ensure work is conducted in line with standard operating procedures, policies and good practices.
Essential Functions
- Study Setup and Planning: Support the Project Manager by attending meetings, preparing minutes and action logs, preparing protocol-specific laboratory instructions documents. Under supervision of the Project Manager oversee setup of protocol specific Laboratory Centralized Monitoring requirements
- Study Activity Monitoring and Closeout: Perform routine tasks across assigned studies including site loading, Investigator Portal access, kit shipments, monitoring day-to-day study performance, overseeing Laboratory Centralized Monitoring. Work with internal and external teams to manage timely resolution of queries and protocol questions, issues and escalations
- Use status reports, monitoring tools and outputs to pro-actively identify trends and provide feedback to internal and external teams on performance of Investigator sites and company services. Support the Project Manager with administrative study tasks
- Coordinate and communicate with relevant stakeholders, including leading Customer communications and activities during any times when the Project Manager is absent. Oversee Project Close-out
- Meetings, Initiatives and Training Activities: May represent company at internal and external meetings, participate in external and internal audits/inspections. As required will support study training with sites, CRAs and customers
- Ensure outputs are delivered in line with organizational standards, protocol specific requirements and Customer expectations
Qualifications
- High School Diploma or equivalent Req Or
- Bachelor’s Degree Life sciences or related field Pref
- 1+ years relevant experience (Clinical, Medical or Healthcare industry preferred). Pref Or
- Equivalent combination of education, training and experience.
- Strong interpersonal, communication, organizational, and time management skills.
- Must be able to comply with all applicable standards as required by the company.
- Demonstrated ability to handle multiple competing priorities and utilize resources effectively.
- Demonstrated ability of critical thinking and problem solving.
- Strong written and verbal communication skills including good command of English language. In certain geographies where communication in local language is desired (e.g. Japan, China), excellent command of local language with reasonable proficiency in English preferred.
- Computer proficiency in word processing, presentation and spreadsheet applications.
- Demonstrated ability to work in a fast-paced environment highly desirable.
- Ability to establish and maintain effective working relationships with coworkers and managers.
If you are looking for some interview questions for the role of Lab Project Svcs Coord at IQVIA then check them out below
- Can you tell us about your experience working in a clinical, medical, or healthcare industry setting?
Answer: I have experience working in a clinical research organization as a clinical research coordinator. In that role, I was responsible for managing day-to-day study activities, including site initiation, enrollment, and monitoring. I am also familiar with good clinical practices and regulations. - How do you ensure that you meet organizational standards, protocol requirements, and customer expectations in your work as a Lab Project Services Coordinator?
Answer: I ensure that I follow standard operating procedures, policies, and good practices to ensure that work is conducted in line with organizational standards. I also make sure to review protocol-specific requirements and customer expectations and communicate with relevant stakeholders to ensure that outputs are delivered according to their needs. - Can you describe a situation where you had to handle multiple competing priorities and how you managed it?
Answer: In my previous role as a clinical research coordinator, I had to manage multiple studies at once, each with their own specific requirements and timelines. To manage competing priorities, I created a detailed task list for each study and prioritized tasks based on their urgency and importance. I also communicated frequently with study teams to ensure that everyone was aligned on priorities. - How do you handle escalations or protocol questions that arise during a study?
Answer: When an escalation or protocol question arises during a study, I first try to gather as much information as possible to understand the issue. I then work with internal and external teams to manage timely resolution of queries and protocol questions. If necessary, I escalate the issue to the Project Manager or other relevant stakeholders. - Can you tell us about a time when you had to participate in an external audit or inspection?
Answer: In my previous role, I participated in several external audits and inspections. To prepare for these events, I ensured that all study documentation was organized and up-to-date. During the audits, I assisted with providing documentation and answering questions. After the audits, I worked with the study teams to address any findings and implement corrective actions as necessary.
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