Medical Writer I
About the Role
Company Overview
Parexel is one of the biggest CROs that specializes in clinical research. It offers its services in the areas of:
Clinical development
Regulatory consulting, and
Market access
Parexel works with pharmaceutical and biotechnology companies to develop new therapies.
The organization is present in many countries and works on all stages of the drugs’ development process. Parexel’s main focus is patient-centered research and high-quality scientific delivery. The company combines its extensive knowledge about regulation with clinical research skills.
Job Summary
The position of Medical Writer I is an entry-level position in the Medical Writing function. The responsibilities of this position include creation and support for the preparation of documents related to clinical and regulatory processes associated with drug development.
The candidate will collaborate with more experienced writers and other groups in order to create the documents that are needed. The position involves strong scientific knowledge. Attention to detail and good communication skills are a plus. The individual will have to be able to multitask.
Key Responsibilities
Responsibilities of the candidate include preparing and assisting with the preparation of clinical and regulatory documents such as clinical study protocol, clinical study report, informed consent form, and patient narratives. The candidate is expected to work with the development of the Investigator’s Brochure and submission documents.
The candidate is expected to work with various teams like clinical research, biostatistics, regulatory affairs, pharmacovigilance, and data management in gathering and interpreting scientific data.
The candidate will be responsible for writing and formatting scientific documents.
The individual is responsible for ensuring all documents are in compliance with the regulations on the global level as well as internal quality standards. The candidate will use the available templates and styles.
The position includes management of assigned tasks within the specified time limits as well as the preparation of project deliverables. The candidate will engage in document reviews and include input received from stakeholders.
The individual will assist in conducting literature reviews and summarizing scientific information if necessary. The candidate will track versions of documents and perform document management.
The individual will be continuously educating themself in medical writing, regulatory requirements, and therapeutic areas..
Qualifications and Skill Requirement
Education-
B.Pharm/ M.Pharm/ PharmD
PhD degree in life sciences or a related field.
Experience: 0-2 years of experience in medical writing, clinical research, or in any other relevant field. Freshers having excellent scientific writing skills can also apply.
It will be helpful if the candidate has some knowledge about clinical research and drug development procedures.
Writing, editing, and proofreading skills are essential. The candidate needs to have the capability to present complicated scientific data clearly.
The candidate needs to have excellent analytical skills.
Communication and teamwork skills are necessary to work with the cross-functional team.
Knowledge of regulatory guidelines like ICH-GCP is an asset.
The candidate should know Microsoft Office tools and document management systems.
Salary and Benefits
Parexel offers attractive compensation packages according to the individual’s experience and credentials. Salary for the job is INR 5.5 to 6.5 LPA.
Working for a global CRO allows employees to be part of international projects.
Training programs, mentoring programs, and onboarding are provided by Parexel to help employees improve their skills. Employees can avail of health benefits, bonuses, and flexible work hours.
Role Importance and Career Growth
This is an essential function to ensure proper documentation in clinical research. This job is crucial when it comes to the process of submitting applications and the approval of medicines. This job will provide a good amount of experience related to the processes of clinical development and regulatory writing.
Career progression typically includes roles such as:
Medical Writer II
Senior Medical Writer, and
Medical Writing Lead
Why Join Parexel
Parexel provides a collaborative and inclusive working environment. Its employees get the chance to work on meaningful projects that have an effect on patients' lives all around the world.
Parexel offers chances to work in a variety of therapeutic areas and documentation formats. Professional development is encouraged by means of training, mentoring, and international experience.
Parexel offers flexibility in terms of work and focuses on work-life balance.
How To Apply
If this is the position you seek to apply for, you should apply through the following procedure:
Create your account in Jobslly.
Search for the position Medical Writer I/ Parexel.
Upload your updated resume.
Upload all the related certificates.
Complete the application form.
Applicants should highlight their writing skills and any experience in clinical research or documentation.
Early application is recommended as positions may close once filled.
Market Insights & Trends
Salary Insights
The amount of money that gets paid can be different depending on how they have been working, where they live and what kind of job they are doing. Some places pay more than others. Most good jobs include extra money for doing a good job, health insurance and flexible hours. Companies pay high salary to make sure they can get the people they want.
Hiring Trends
The number of jobs for this profile is going up every year. Hospitals and other healthcare companies are looking for people who're good, at their job and can also figure out new problems. They want who can do the work and also think on their feet to deal with the challenges of working in healthcare today.