Senior Clinical Research Associate (West, Dermatology)

30.01 Premier Research Group (India) Private Limited; United States; Remote; USD 105,000; Full time

Job summary

A leading clinical research organization is seeking a Senior Clinical Research Associate to oversee clinical trials in dermatology. This remote role requires an undergraduate degree and at least four years of experience in clinical research monitoring, with a strong emphasis on data integrity and patient safety. You'll play a vital role in transforming life-changing ideas into new treatments while ensuring high-quality communication with investigative sites.

Benefits

Comprehensive benefits package including health insurance

Retirement plans

Paid time off

Qualifications

• 4+ years of clinical research monitoring experience required.
• Experience with dermatology studies highly preferred.
• Must meet travel requirements (70-85%).

Responsibilities

• Perform monitoring activities for Phase I-IV clinical trials.
• Ensure data integrity and patient safety.
• Primary contact for investigative sites and manage project tasks.

Skills

Customer-focused approach

Organizational skills

Collaboration

Accountability

Education

Undergraduate degree or equivalent

Job description

Senior Clinical Research Associate (West, Dermatology) page is loaded

Senior Clinical Research Associate (West, Dermatology)

Apply remote type Remote locations United States of America Regional_MN Regional_IN Regional_CO Regional_MO time type Full time posted on Posted 6 Days Ago job requisition id R5398 Premier Research is looking for a Senior Clinical Research Associate (West, Dermatology) to join our Global Clinical Monitoring and Site Management 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 Built for You. 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.

• We are Built by You. Your ideas influence the way we work, and your voice matters here.

• We are Built with You. As an essential part of our team, you help us deliver the medical innovation that patients are desperate for.

Together, we are Built for Biotech. Join us and build your future here.

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: Dermatology

• 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 along with minimum of 4+ years previous clinical research monitoring experience required.

• Experience with dermatology studies highly preferred

• Must be located in the following states: WA, UT, NV, AZ, OR, CA

• 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

• Organized team player, collaborative and able to build and maintain an effective team with a positive, results-oriented work environment

• Accountable, dependable and strong commitment

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

• Valid driver’s 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 candidate’s 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.

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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