IQVIA Medical Trainee Job – Entry Level Role For Life Sciences, Apply Online

Job Family Description

Writes, reviews, and coordinates preparation of clinical trial documentation in line with client specifications and industry practices.

Sub-Family Description

Prepares, or contributes to the preparation of clinical and regulatory documents for external clients, for investigational drugs, biologicals, or medical devices.

Collaborates with internal and external experts and specialists and maintains expertise on developments in a particular field of focus.

JOB OVERVIEW

Job Profile Summary

An entry-level role within a structured program, supporting Medical Writing deliverables and focusing on specific tasks under senior supervision, while gaining experience, knowledge, and skills in Medical Writing.

Keeps abreast of current medical and/or technical writing/regulatory knowledge, including GCP, along with developments and advances in drug development/medical and/or technical writing.

Responsibilities

Essential Functions

• Gain knowledge, experience, and competence in specific Medical Writing tasks by supporting Medical Writing senior staff in managing client requests under supervision, focusing on tasks such as writing patient narratives.
• Manage day-to-day workload, track timelines, draft assigned documents to a high standard, and implement review comments and customer requests with senior guidance/review, keeping manager/senior staff abreast of progress on tasks and any potential problems.
• Interact with internal clients. May have some external interactions, mostly directed by senior staff.
• Keep abreast of current data, trends, medical and/or technical writing/regulatory knowledge, developments and advances in area of drug development/medical and/or technical writing.
• Comply with customer requirements and with IQVIA SOPs and standards.

MINIMUM REQUIRED EDUCATION AND EXPERIENCE

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Experience

This is an entry-level trainee position and as such education, skills, and potential are more important than formal work experience. However, experience and strong ability in scientific writing in English gained from academic studies or work experience are essential.

Knowledge

Awareness of drug development, medical writing, and associated regulations. Good understanding of statistical principles and of medical terminology across a range of therapeutic areas.

Education

Education Level

Education Details

Req

Pref

• Bachelor’s Degree (BAMS, BHMS, BDS)  – Life science-related discipline or related field
• Advanced Degree (MPharm, MSc or PhD) – Life science-related discipline or related field

Additional Work Experience

Experience Details

Req

Pref

• Familiarity with the structural and content requirements of clinical study reports, protocols, and similar documents.
• Good understanding of common statistical methods used in clinical trials and/or interpretation of their results.
• Ability to integrate, interpret, and summarize data from a variety of sources in a clear and concise manner.

Skills and Abilities

• Excellent written and oral communication skills including grammatical/technical writing skills.
• Excellent attention to detail and accuracy.
• Communicates clearly, effectively and confidently with others.
• Demonstrated abilities in collaboration with others and independent thought.
• Demonstrates confidence and maturity in most routine medical writing situations.
• Demonstrates good judgement in requesting input from senior staff.
• Ability to establish and maintain effective working relationships with coworkers, managers and customers.
• Ability to effectively manage multiple tasks and projects.
• Must be computer literate.

Standard ADA Settings

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions

Standard ADA Selection

Office Environment

• Extensive use of telephone and face-to-face communication requiring accurate perception of speech.
• Extensive use of keyboard requiring repetitive motion of fingers.
• Regular sitting for extended periods of time.

May require occasional travel.

APPLY ONLINE

If are you looking for some interview questions for the Medical Writing Trainee only at IQVIA, then check the bottom of the page.

1. Can you explain your understanding of medical writing and its importance in clinical trial documentation?
   • Answer: Medical writing plays a crucial role in preparing clinical trial documentation that adheres to client specifications and industry practices. It involves writing, reviewing, and coordinating the creation of documents related to investigational drugs, biologicals, or medical devices. These documents are essential for regulatory submissions and provide critical information about the study design, patient narratives, and other relevant aspects. Medical writers ensure accuracy, clarity, and compliance with regulatory guidelines.
2. How would you manage your workload and track timelines while working on medical writing tasks under senior supervision?
   • Answer: Managing workload and tracking timelines are essential for effective medical writing. I would prioritize tasks based on urgency and importance, ensuring that deadlines are met. I would maintain a detailed work plan, track progress, and communicate regularly with my manager and senior staff to keep them informed about the status of assigned documents. I would also be proactive in seeking guidance and clarification when needed to ensure smooth workflow and timely completion of tasks.
3. Can you discuss your experience or familiarity with the structural and content requirements of clinical study reports and protocols?
   • Answer: During my academic studies or previous work experience, I have gained familiarity with the structural and content requirements of clinical study reports and protocols. I understand the importance of clear and concise presentation of data, adherence to specific sections and headings, and compliance with regulatory guidelines. I have also been exposed to the interpretation and summary of data from various sources, ensuring accuracy and relevance in the final documents.
4. How do you ensure accuracy and attention to detail in your medical writing? Can you provide an example of a situation where attention to detail was critical in your work?
   • Answer: Accuracy and attention to detail are paramount in medical writing. I meticulously review my work, double-checking for grammatical and technical errors. I pay close attention to data consistency, formatting, and adherence to specific guidelines. In a previous project, I was responsible for preparing a safety summary report. The report required precise documentation of adverse events and their associated data. By meticulously reviewing each entry, cross-referencing with source documents, and ensuring consistency, I successfully produced an accurate and comprehensive report.
5. How do you stay updated with developments and advances in drug development and medical writing? Can you provide examples of how you have applied this knowledge in your work?
   • Answer: Staying updated with developments and advances in drug development and medical writing is crucial for maintaining high-quality work. I actively engage in continuous learning by following industry publications, attending relevant webinars, and participating in professional development opportunities. For example, I recently attended a workshop on the latest regulatory requirements for clinical study reports. I applied this knowledge by incorporating the updated guidelines into my writing, ensuring compliance and enhancing the quality of the documents I prepared.

Note: These are sample questions and answers. It is important to personalize the answers based on the individual’s experience and expertise in medical writing.

Editor’s Note: IQVIA Medical Trainee Job – Entry Level Role For Life Sciences, Apply Online. IQVIA Medical Trainee Job 2023. Please make sure that you are subscribed to the Biotecnika Times Newsletter and our YouTube channel to be notified of all of the latest in the industry. Follow us on all of our social media like Twitter, Telegram, Facebook and Instagram.