Analyst, Clinical Patient Screening

Edwards Lifesciences • Irvine, CA

4d

About The Position

Patients with mitral and tricuspid heart valve disease often have complex conditions with limited treatment options. Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address a patient’s unmet clinical needs. It’s our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey. The Analyst, Clinical Patient Screening will manage workflows for commercial patient screening.

Requirements

• Bachelor's Degree in relative field of study (Biological Sciences, Lifesciences preferred) or equivalent work experience based on Edwards criteria required
• Minimum of three (3) years experience in patient screening or clinical trial setting experience

Nice To Haves

• Certified Clinical Research Professional (CCRP), Society of Clinical Research Associates (SOCRA)
• Proficient in Microsoft Office Suite (including Word, Excel, PowerPoint and related applications)
• Demonstrates professional communication and interpersonal relationship management skills across all organizational levels
• Efficient in basic problem-solving, organizational, analytical and critical thinking skills
• Moderate knowledge and understanding of clinical studies as it relates to policies, procedures, and guidelines.
• Moderate understanding of medical terminology as it relates to clinical studies
• Ability to manage confidential information with discretion and strict attention to details
• Thrives in a collaborative, matrixed team environment, including inter-departmental teams and representing the organization on specific projects
• Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control

Responsibilities

• Designing and developing site trainings and required materials for trials including protocols, case report forms, webinars, and additional training materials in partnership with cross-functional stakeholders
• Provide input for clinical and pre-clinical screening strategy and process
• Develop and maintain site relationships by performing all site communication correspondences.
• Assist trial leads with expediting day-to-day tasks (i.e. - pulling core lab priority lists)
• Collaborate with trial leads on screening methodologies based on device limits, imaging assessments, and procedural capabilities
• Lead internal screening calls with cross-functional teams to move patients through the screening process.
• Provide communications on day-to-day in regards to screening.
• Other incidental duties as needed

Benefits

• competitive salaries
• performance-based incentives
• a wide variety of benefits programs to address the diverse individual needs of our employees and their families

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 5,001-10,000 employees