Intern, Clinical Safety
Position Overview
Salary: $21 -$34/hour. Compensation packages may be higher/lower than what is listed, & will ultimately depend on factors including relevant experience, education and class level.
This internship offers a hands-on opportunity to gain practical experience in the processes that ensure the safety of our medical devices and therapeutic products throughout clinical development. The intern will develop a comprehensive understanding of safety review workflows and contribute to various activities aimed at identifying, reviewing and adjudication of adverse event data.
Job Duties:
This internship offers a hands-on opportunity to gain practical experience in the processes that ensure the safety of our medical devices and therapeutic products throughout clinical development. The intern will develop a comprehensive understanding of safety review workflows and contribute to various activities aimed at identifying, reviewing and adjudication of adverse event data.
Job Duties:
- Gain working knowledge of safety review workflows including adverse event and technical event review, CEC adjudication and MedDRA coding of adverse events.
- Assist in the execution and documentation of clinical safety reviews for ongoing studies.
- Contribute to continuous improvement initiatives for safety review processes and documentation practices.
- Support the preparation and review of safety documentation (e.g., narratives, source documents for CEC meeting, and review meeting minutes)
- Qualifications:
- Currently pursuing a degree in Medicine, Life Sciences, Public Health, Nursing, Pharmacy, or related field (graduate students preferred)
- Strong interest in clinical safety, or clinical research
- Excellent attention to detail and organizational skills
- Strong written and verbal communication skills
- Ability to work independently and collaboratively in a fast-paced environment
- Proficiency in Microsoft Office (especially Excel and Word)
What you will learn:
- In-depth exposure to safety workflows across the clinical trial lifecycle.
- Experience working in a highly collaborative environment within a regulated industry.
- Insight into how clinical safety decisions impact patient protection.
- Opportunities to build professional skills and network with cross-functional teams.
- Extended periods of computer use
- Extended periods of sitting, standing, or speaking
- Light lifting, up to 25 lbs
EEO
We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to race, national origin, gender, age, religion, disability, sexual orientation, veteran status, marital status or any other characteristics protected by law.
Fair Chance Ordinance If you are applying to perform work for Terumo Neuro in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Terumo Neuro reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Terumo Neuro will consider for employment qualified job applicants with arrest or conviction records in accordance with the California Fair Chance Act, Los Angeles County Fair Chance Ordinance for Employers, Fair Chance Initiative for Hiring Ordinance, and San Francisco Fair Chance Ordinance.
- Qualifications: