Trainee Medical Writer at Parexel For Life Sciences Candidates, Apply Online
Trainee Medical Writer at Parexel For Life Sciences Candidates, Apply Online. Parexel Hiring MSc & PhD Life Sciences vacancy. Parexel has job openings for life sciences candidates. Check out all of the details on the same below
Hey there, looking for some assistance with the possible interview questions and answers for the role of Trainee Medical Writer at Parexel, then check below
Name of the Post – Trainee Medical Writer
Job ID R0000011777
Bengaluru, Karnataka, India
When our values align, there’s no limit to what we can achieve.
At Parexel, we all share the same goal – to improve the world’s health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special – a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we’re committed to making a difference.
Trainee Medical Writer
Job Description:
- Gather, review, analyze, and evaluate pertinent resources to prepare, develop, and finalize low complexity documents, such as patient narratives, public disclosure documents, and simple aggregate safety reports (e.g., Periodic Adverse Drug Experience Report [PADERs]), under supervision of the project medical writer or other appropriate departmental supervision.
- With appropriate departmental supervision and mentoring, provide writing support for more complex clinical documents, such as informed consent forms (ICFs) and clinical study reports (CSRs)/CSR shells. This could involve writing certain sections or supporting the Lead Medical Writer on specific authoring tasks. Provide direction to Document Specialists for appendices compilation and related tasks, as required.
- Revise document drafts based on the review comments from team members to ensure inclusion of all relevant input.
- Ensure that all work is complete and of high quality prior to team or client distribution. Confirm data consistency and integrity across the document.
- Follow required standard operating procedures (SOPs), templates, guidelines, regulations, client instructions and other processes, as applicable.
Job Qualifications
- Excellent interpersonal, verbal and written communication skills.
- Ability to consistently produce documents of high quality.
- Demonstrates attention to details and proactivity.
- Ability to understand all necessary steps in a project, plan steps ahead, and identify critical paths.
- A flexible attitude with respect to work assignments and new learning; readily adapts to changes.
- Ability to efficiently manage time spent on tasks and proactively identify deficiency. Managemultiple and varied tasks with enthusiasm and prioritize workload with attention to detail, e.g., organizational skills.
- Willingness to work in a matrix environment, values the importance of teamwork, andunderstands roles of other project team members.
- Strives to understand and satisfy client needs.
- Exhibits knowledge of regulatory documents and ICH-GCP guidelines.
- Scientific background essential; some experience of pharmaceutical industry and anunderstanding of clinical research are preferred.
- Knowledge or ability to learn software and systems: MS Office (Word proficiency required),document management systems, collaborative authoring (e.g., SharePoint), file conversion anddatabases (Excel).
- Fluent in written and spoken English with appropriate attention to phraseology, grammar, andpunctuation.
Master’s degree or PhD in Life Sciences/Health Related Sciences or equivalent. Pass out year 2022 and 2023.
Location: Open in India
Hey there, looking for some assistance with the possible interview questions and answers for the role of Trainee Medical Writer at Parexel, then check below
- Can you describe your understanding of the role of a medical writer in the pharmaceutical industry? Answer: A medical writer plays a crucial role in preparing, developing, and finalizing clinical documents. They gather and analyze relevant resources to create documents such as patient narratives, public disclosure documents, and safety reports. They also provide support in writing more complex documents like informed consent forms and clinical study reports.
- How do you ensure the quality and accuracy of your written documents? Answer: I pay close attention to details and proactively review my work to ensure accuracy and completeness. I follow standard operating procedures, guidelines, and regulations to maintain consistency and integrity across the document. I also rely on feedback from team members to incorporate relevant input and make necessary revisions.
- Can you provide an example of a project where you had to manage multiple tasks and prioritize your workload effectively? Answer: In a previous project, I was responsible for writing patient narratives, compiling appendices, and supporting the Lead Medical Writer in authoring tasks. To manage these tasks efficiently, I created a detailed plan, identified critical paths, and prioritized my workload based on deadlines and project requirements. This allowed me to successfully complete all tasks on time while maintaining a high level of attention to detail.
- How do you approach working in a team and collaborating with other project team members? Answer: I value the importance of teamwork and understand the role of each team member in achieving project goals. I actively contribute to the team, share knowledge and ideas, and communicate effectively to ensure smooth collaboration. I am open to feedback and willing to adapt to changes, fostering a positive and productive work environment.
- What steps do you take to stay updated with regulatory guidelines and industry best practices? Answer: I continuously stay informed about regulatory documents and adhere to ICH-GCP guidelines. I actively participate in professional development activities, such as attending seminars, webinars, and workshops. I also keep track of relevant publications and industry news to stay up to date with the latest advancements and best practices in the field of medical writing.
Note: These are sample interview questions and answers. It’s important to tailor the questions according to the specific requirements of the job and the organization.
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