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Open nowPosted 21 days ago

In-House Clinical Research Associate II, Sponsor-Dedicated (Contract)

Premier Research82 open roles

Where
United States of America
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Your applicationOpen nowIn-House Clinical Research Associate II, Sponsor-Dedicated (Contract)Premier Research · United States of America

  1. YouYes, apply to this one.

  2. CV RocketCV written for this posting.

  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

  4. CV RocketApplied on Premier Research's own form.

The reply lands in your private mailbox

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The clock on this job

Early applications get read.

13.3% of postings close within 7 days. Measured by our own scanner across the market. Premier Research postings stay open a median of 17 days.

Share of postings closed within
  1. 2.1%1 day
  2. 4.6%3 days
  3. 13.3%7 days
  4. 21.3%14 days
  5. 35.7%30 days
  6. 59.1%60 days
This job: posted 21 days ago

Premier Research median: 17 days open

The posting

Premier Research is looking for a In-House Clinical Research Associate I, Sponsor-Dedicated (Contract) to join our Functional Services Provider (FSP) team.

You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success.

  • We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires.
  • Your ideas influence the way we work, and your voice matters here.
  • As an essential part of our team, you help us deliver the medical innovation that patients are desperate for.

Join us and build your future here.

What you'll be doing:

  • Partners with cross-functional team members and study sites throughout all phases to offer support of numerous trial elements for the clinical operation teams.
  • Carry out remote monitoring of clinical trials
  • Serves as the secondary contact for sites supporting CRAs
  • Responsible for the proper reporting and follow up of SAEs and ensures all reportable events are identified, clearly documented and reported per protocol as well as applicable requirements and regulations
  • Ensures any identified non-compliance issues are addressed, clearly communicated, documented and escalated as required through monitoring visits, analyzing study metrics, and general study data overview
  • Assists with audit/inspection readiness, study start-up activities, data listing reviews, monitoring visit support and issue resolution

​

What we are searching for:

  • Experience in Neurology or Psychiatry, including work with Schedule I controlled substances, is highly preferred
  • Bachelor's degree, or international equivalent from an accredited institution, preferably in a clinical, biological, scientific, or health-related field or equivalent combination of education, training and experience
  • 3 to 5 years of practical experience in clinical trials. Alternately, a proven experience in all primary job functions
  • Participate in study-specific meetings, teleconferences and training as needed
  • Demonstrates excellent English verbal and written communication skills
  • Proven ability to drive a successful customer experience through positive customer interactions, provision of quality and timely deliverable, and task ownership
  • Preferred Location: East Coast / Central

This is a 1099 12-month contract position with the potential to extend and renew after 1 year.

Premier Research is proud to be an equal opportunity employer that is compliant with all federal guidelines. All qualified applicants will receive equitable consideration without regard to race, color, religion, sexual orientation, gender identity, national origin, disability or veteran status

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