medical reviewer/safety reviewer ii.

• north chicago , illinois (remote)

• posted april 19, 2024

job details

summary

• $34 - $49.93 per hour

• contract

• bachelor degree

• category life, physical, and social science occupations

• reference47945

job details

job summary:

As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is for you!

location: North Chicago, Illinois

job type: Contract

salary: $34.00 - 49.93 per hour

work hours: 9 to 5

education: Bachelors

responsibilities:

• Provides timely assessment of reported clinical trial data and participates in applicable safety surveillance activities for assigned studies including review of labs, vital signs, cardiac, medications, medical history, and can communicate with Study Lead any findings.

• Provide review of safety-related data from clinical trials for content, quality, potential study level trend identification, and adherence to regulatory guidance and protocols utilizing critical thinking skills.

• Monitoring of safety-related queries to Investigators.

• Adheres to regulatory guidance, protocols, departmental processes and policies under minimum supervision.

• Current with knowledge of ICH, FDA, and EMA regulatory guidance's affecting safety surveillance.

qualifications:

• Bachelor's degree with related health science background. RN or clinical pharmacy experience strongly preferred.

• A minimum of 2 years of clinical practice experience is required and 1-year drug safety experience preferred.

• Strong critical thinking skills with the ability to clinical knowledge to adverse event data collection and data assessment.

• Ability to present accurate and medically sound safety data, both orally and in writing.

• Effective communication skills in delivering study-related information.

• Proficiency in Computers (Windows, Word, Excel).

skills: FDA, MS-WORD, MS-EXCEL, SAE (Serious Adverse Event), ICH Regulations, AD (Adverse Events)

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).

Applications accepted on ongoing basis until filled.