Clinical Research Associate Job at ViewRay, Inc.
Job Title: Clinical Research Associate, Clinical Affairs
Location: Denver, CO - hybrid
About ViewRay
ViewRay®, Inc. (Nasdaq: VRAY) designs, manufactures, and markets the MRIdian® radiation therapy system. MRIdian is built upon a proprietary high-definition MR imaging system designed from the ground up to address the unique challenges and clinical workflow for advanced radiation oncology. Unlike MR systems used in diagnostic radiology, MRIdian's high-definition MR was purposely built to deliver high-precision radiation without unnecessary beam distortion, and consequently, help to mitigate skin toxicity and other safety concerns that may otherwise arise when high magnetic fields interact with radiation beams.
At ViewRay, our vision is clear. We are dedicated to proving and treating what others can't.
At ViewRay, our vision is clear. We are dedicated to proving and treating what others can't.
We are an entrepreneurial company with big ambitions, unlimited potential, and a passion for improving the lives of patients with cancer. We are always on the lookout for talented people who share our commitment and values. Contact us if you are enthusiastic about working with a close-knit team and motivated by the prospect of making a difference.
The Vision for Success
At ViewRay, attracting, developing, and retaining talent is at the center of everything we do. As a Clinical Research Associate (CRA), you will be tasked with managing multiple sponsored clinical studies. You will have oversight of the site selection, qualification and initiation process. Good Clinical Practice and compliance are key components that a CRA will maintain for the study. You will also help to manage interactions with a CRO, and you will support all aspects from study start-up through follow-up and closure.
We are looking for an experienced communicator, someone who is comfortable speaking with research staff and physicians. We need someone who rises to a challenge, can problem solve, is driven to succeed and understands the work required to do so. Importantly, we must find someone who possesses the organizational ability and subject matter expert to oversee clinical studies. In this role, you will:
- Support clinical trial management of a multi-center, randomized study
- Protocol development
- Oversee study to ensure that it complies with protocols, is ethically-conducted and follows regulatory standards
- Maintaining research records of study activity, including case reports forms, agreements, or other regulatory forms as per FDA guidelines
- Communication with the medical site staff including coordinators, clinical research physicians, and their site staff;
- Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff;
- Conduct qualification and initiation visits at research sites in compliance with the approved protocol;
- Regulatory document review;
- Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol; and
- Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement
The Value you Will Bring
- Minimum of 2 years experience with site management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology;
- Must have a minimum of a Bachelor’s degree in a health or science related field;
- Ability to travel to locations nationwide is required; some visits may be conducted remotely;
- Strong verbal and written communication and presentation skills;
- Must be detail-oriented and efficient in time management;
- Strong organizational skills; and
- Strong computer skills, including but not limited to the knowledge of a Clinical Trial Management System (CTMS) and MS-Office products such as Excel and Word
Why you will see yourself here
At ViewRay, our teammates challenge conventional thinking and are motivated to change the standard of care in radiation therapy.
Plus, we offer great benefits, including:
- Health, dental, and vision insurance that begins on your first day of employment
- 401(k) plan with company match and immediate vesting period
- Generous paid time off and flexible schedule
- Office stocked with snacks, drinks, and occasional catered meals
- Fun collaborative team with quarterly social events
ViewRay is an EEO employer.
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