Associate, Medical Writing (MD)

ClinChoice is a global full-service CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative “one-team” culture. We are looking for a dynamic person to join our in-house team as an Associate, Medical Writing (MD) on a permanent basis.

Join our team: you can be part of making a difference in peoples’ lives and experience a fulfilling and rewarding career!

The Medical Writer acts as a team member supporting and executing the creation and updating of Clinical Evaluation Reports (CER), Summary of Safety and Clinical Performance Reports (SSCP), State of the Art Reviews (SOA) and Systematic Literature Reviews (LRR) for their assigned therapeutic area within Depuy Synthes.

• Performs tasks according to the assigned medical writing activities including systematic literature reviews primarily for the generation of Clinical Evaluation Reports (CER), Summary of Safety and Clinical Performance (SSCP), State of the Art (SOA), Post-Market Surveillance (PMS) including Periodic Safety Update Reports (PSUR), and Premarket Approval (PMA) Food and Drug Administration (FDA) Reports, including Humanitarian Device Exemption (HDE), Investigative Device Exemption (IDE) Reports, and Health Economics and Market Access (HEMA) research. The specific tasks are to be determined based on the assigned role in the project.

• Alerts and escalates to senior members as required, whenever project deliverable risks are visualized, OR issues are encountered impacting the delivery schedule.

• Ensures error free and acceptable quality of assigned deliverables.

• Responsible for ensuring training compliance and timesheet compliance.

• Ensures that all assigned goals (e.g., utilization and efficiency) are met as per set standards for the performance year.

• Follows and complies with the Company’s Code of Conduct, Policies, and Procedures.

• Responsible for confidentiality, integrity, availability, and safeguarding of data.

• Responsible for reporting of security incidents and PIMS breaches as applicable.

• Complies with company QMS, ISMS, and PIMS requirements and applicable regulatory requirements.

• Demonstrates adherence and compliance to PIMS/GDPR requirements as follows: data processed fairly, transparently, and lawfully; collected for specified and legitimate purposes; adequate, relevant, and limited to the specified purposes; processed in a secure manner.

• Proficiency in oral and written English language.

• Proficiency in Microsoft Office Suites (e.g. Word, Excel, PPT, SharePoint).

• Minimum bachelor’s degree in any life sciences field and at least 1 year of experience in medical writing, or any related field as applicable, OR

• Advanced/Post graduate degree in Medicine or life science (i.e. Master’s in Public Health) with any professional experience.

• Can work in a diverse team environment.

• Good analytical and comprehension skills.

• Proficient in time management and can work with minimal supervision.

• Flexible Working Hours

• Team events and end of year party

• Employee satisfaction survey - your feedback is important for continuous improvement

• Health Insurance

The Application Process

Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not