clinical research associate in monroeville

posted
job type
contract
salary
US$ 30 per hour
apply now

job details

posted
location
monroeville, pennsylvania
job category
Information Technology
job type
contract
salary
US$ 30 per hour
reference number
630456
phone
.
apply now

job description

job summary:

We are looking for a Clinical Research Associate (CRA) in Monroeville, PA (travel in the NE is required)

This position will be supporting clinical research trials for AED device studies. There is a Sr. Clinical research Associate on the team who is getting the study off the ground. This person will then handle the day to day management and monitoring of the study.

Travel will be required 50%-75%. The study will involve 5-10 sites geographically in the northeast, especially with the team in Andover. They will be contracting sites for the study, so this person will need to travel there to train and provide monitoring. These will be short trips, 1-2 days at a time, but will be ongoing throughout the study.

The person will sit in Monroeville, but will have flexibility to WFH 1-2 days/week once they are up and running. They will also be travelling frequently, especially at the beginning of the study.

This will be a long term contract role, starting off at 1 year with anticipation of multi-year extension or possible permanency down the road.

 
location: Monroeville, Pennsylvania
job type: Contract
salary: $30 - 40 per hour
work hours: 8 to 5
education: Bachelors
 
responsibilities:

This person will be responsible for:

  • Managing the study
  • Monitoring clinical trials
  • Overseeing data entry
  • documentation review and study management
  • IRB (Internal Review Board) submissions
  • Execution of study
 
qualifications:

BS Degree is REQUIRED - anything scientific is fine, biomedical, chemistry, biology, etc.

 
skills: Skills and Experience:

Minimum 3 Years experience in a Clinical Research Associate (CRA) role - this is an industry standard job title and should be on their resume.

This is a mid-level role, 5 years experience in Clinical Trials is sufficient, but they should have specific experience monitoring clinical trials. If they have managed a complete study that would be a big plus, but they should be a well versed CRA with Monitoring experience.

Experience can be Medical Device OR Pharma, with a preference for med device, but it is not required.


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.

skills

Skills and Experience:

Minimum 3 Years experience in a Clinical Research Associate (CRA) role - this is an industry standard job title and should be on their resume.  

This is a mid-level role, 5 years experience in Clinical Trials is sufficient, but they should have  specific experience monitoring clinical trials.  If they have managed a complete study that would be a big plus, but they should be a well versed CRA with Monitoring experience. 

Experience can be Medical Device OR Pharma, with a preference for med device, but it is not required.  

 

qualification

BS Degree is REQUIRED - anything scientific is fine, biomedical, chemistry, biology, etc.  

responsibilities

This person will be responsible for:

  • Managing the study
  • Monitoring clinical trials 
  • Overseeing data entry 
  • documentation review and study management 
  • IRB (Internal Review Board) submissions 
  • Execution of study

educational requirements

Bachelors