Senior CRA, Onc/Neuro/Rare/Derm (West Coast, Midwest, Northeast)

Premier Research

$105K *
US-AnywhereRemote in United States
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Undergraduate degree or equivalent required.
  • 4+ years of previous on-site clinical research monitoring experience.
  • Experience with oncology, neurology, rare disease, and dermatology studies.
  • Customer-focused with effective communication skills.
  • Ability to meet travel requirements of 70-85% and 8-10 days on-site/month.
  • Residing in the West Coast, Northeast, or Midwest regions.
  • Valid driver's license and passport as needed.

Responsibilities

  • Perform monitoring activities including on-site and remote visits for clinical trials.
  • Ensure clinical data validity and patient safety according to protocols and regulations.
  • Serve as primary contact for investigative sites, managing queries and project tasks.
  • Identify and escalate risks and retraining opportunities at investigative sites.
  • Schedule and plan day-to-day monitoring activities and complete high-quality trip reports.

Benefits

  • Comprehensive health insurance.
  • Retirement plans.
  • Paid time off.
Full Job Description
Premier Research is looking for a Senior CRA, Onc/Neuro/Rare/Derm (West Coast, Midwest, Northeast) to join our Clinical Monitoring, Site Management and SSU team.

What you'll be doing:

  • Perform monitoring activities (both on site and remote) including Site Qualification Visits, Site Initiation Visits, Interim Monitoring Visits, Site Management Contacts, Close Out Visits for Phase I-IV clinical trials, as well as device trials with opportunities to work in the following Therapeutic areas: oncology, pediatrics, rare disease.

  • Ensure the validity, correctness, and completeness of clinical data collected at sites with a focus on data integrity and patient safety as dictated by trial protocol, ICH-GCP/ISO 141155, and customer requirements.

  • Serve as the primary point of contact for investigative sites, manage query resolution, support Trial Master File activities, participate in Investigators’ Meetings, and complete other project tasks in accordance with study timelines and budget.

  • Identify and escalate potential risks and possible retraining opportunities for investigative sites.

  • Schedule and plan day-to-day activities to include study monitoring visits, timely completion of high quality trip reports, and active management of all deliverables.

What we are searching for:

  • Undergraduate degree required or its international equivalent, along with minimum of 4+ years previous on-site clinical research monitoring experience required.

  • Known for being customer-focused in approach to work and communications with the ability to professionally interact with sites, clients, vendors and other functional areas

  • Experience with monitoring oncology/neurology/rare disease/dermatology studies are required

  • Accountable, dependable and strong commitment

  • Ability to meet the requirement of 8-10 DOS (Days on site)/monitoring visits/month; 70-85% travel

  • You must live in the West Coast, North East, or Midwest Regions

  • Valid driver27s license, passport as required

Premier Research is dedicated to providing compensation that is fair and competitive with market standards. The annualized starting base pay for this role is $105,000.00 USD. The actual salary will be influenced based on a variety of factors such as the candidate27s qualifications, skills, competencies, and proficiency for the role. We also offer a comprehensive benefits package, which may include health insurance, retirement plans, and paid time off.

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