Clinical Research Coordinator- Warren, NJ (Temp to Perm)

Responsibilities

• Cook up clinical trials according to protocols and Standard Operating Procedures (SOPs)
• Chat with sponsors, contract research organizations (CROs), clinical research associates (CRAs), institutional review boards (IRBs), and site staff
• Help out investigators and make sure all the study docs are legit (ALCOA)
• Report any bad stuff that happens and keep the study data squeaky clean

Qualifications

• Two or more years of clinical research experience with phlebotomy skills
• A bachelor’s degree required (a master’s degree is nice)
• Can handle lots of studies at once without breaking a sweat
• Has a CCRC certification if you can get it

Benefits (upon conversion)

• Medical, dental, and vision insurance
• Paid time off, holidays, and floating holidays
• 401(k) with an employer match
• Tuition reimbursement and student loan repayment assistance
• Paid parental leave
• No on-call responsibilities