Senior Clinical Research Associate I

Scorpion Therapeutics; United States; Remote; USD 70,000 - 90,000; Full time

Job summary

A leading company in the clinical research sector is seeking a Senior Clinical Research Associate I for a full-time position based in Minneapolis, Minnesota. The role involves monitoring clinical trials, ensuring compliance with regulations, and developing study protocols. The company offers a stimulating work environment, career development opportunities, and flexible work options.

Benefits

Stimulating work

Project diversity

Intellectual challenge

Agile & flexible workplace

Opportunity to progress

Stability

Sense of community

Great tools / tech

Competitive salary

Qualifications

• 4 to 5 years of experience as a SCRA in the pharmaceutical or CRO industry.
• Solid knowledge of drug development process and clinical trial monitoring procedures.

Responsibilities

• Act as the primary link between sites and sponsor, responsible for monitoring and documentation.
• Prepare ethics submissions and assist in Clinical Study Reports.

Skills

Clinical trial monitoring

GCP guidelines

Medical terminology

Initiative

Autonomy

Education

Degree in science or healthcare-related discipline

Job description

If you're aiming for a job like this, you need an edge.

JobsAI gives you that edge—by helping you upgrade your resume, analyze hiring managers’ LinkedIn profiles, and prepare with a built-in interview coach.

This is the smarter, faster way to compete in today’s job market.

Check out JobsAI

Avance Clinical

Our most important asset is our people. We offer a work environment and a culture that values honesty and respects its people.

Avance Clinical is a Contract Research Organization which offers specialized services supporting clinical drug development for the pharmaceutical and biotechnology industry.

Opportunity

This is a full-time permanent position for a Senior Clinical Research Associate I based in the US. We are looking for candidates specifically in Minneapolis Minnesota.

As we continue to grow, we want our people to grow with our organization. We offer training and career development opportunities to build the skills and progress the careers of our employees.

Responsibilities

Acting as the primary link between sites and sponsor, you'll be responsible for:

• Performing start-up, initiation, monitoring, and close-out visits along with maintaining appropriate documentation
• Developing your skills and knowledge on clinical trials within a wide scope of therapeutic areas
• Monitoring all aspects of studies to ensure compliance with GCP, study protocol and regulatory requirements, and prepare monitoring reports
• Development and review study protocols and other study-related documents
• Preparing ethics submissions and assisting in the preparation of Clinical Study Reports.

Requirements

Prior experience monitoring clinical trials. A degree in science or other healthcare-related discipline. Ideally between 4 to 5 years of experience working as a SCRA in the pharmaceutical or CRO industry. Solid knowledge of drug development process, clinical trial monitoring procedures, GCP guidelines, and medical terminology are essential. On top of this, you will need to be able to show initiative and work well autonomously, within minimal supervision.

What we offer

• Stimulating work
• Project diversity
• An intellectual challenge
• An agile & flexible workplace
• Opportunity to progress
• Stability
• Sense of community
• A leadership team that are working together on a common goal
• Flexible work options
• Great tools / tech to do your job
• A competitive salary

What next?

As a growing business we’re looking for likeminded people to join us - we hope that’s you.

To join our team please submit your CV & cover letter as one Microsoft Word document. To apply for this role please click on the 'APPLY' link and submit your CV along with a cover letter. The cover letter should document why you would make a great addition to the Avance Clinical team. Please submit the CV and cover as one document.

As we receive a high volume of applications for our vacancies, we will only contact you directly, should you be successful through to the next stage of our recruitment process. No agencies please.