Philadelphia, PA, USA
Posted: Nov 21, 2024
RemoteFull-time
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Nice To Have skills
Job Description
Clario is a 50+ year old company that delivers industry leading clinical trial endpoint technology solutions. The future of clinical trials is vibrant, with new technologies revolutionizing what’s possible. From new trial modes to faster and integrated evidence and findings, our innovative clinical trial solutions mean we can unlock better evidence.

What We Offer

  • Competitive compensation
  • Medical, dental, and vision insurance beginning Day 1 of employment
  • Flexible work schedules
  • Attractive PTO plan
  • Engaging employee programs
  • Remote working

What Youll Be Doing

Maintains Quality Service and Departmental Standards by:

  • Work within Clario and externally with cardiologists, sonographers, technologists, scientists, software engineers, and operational specialists on study documentation, scan acquisition quality control, and image analysis
  • Develop various imaging protocol documents in the support of a clinical trial protocol, study contract, or a client’s regulatory submission
  • Investigate current industry literature, technology, methodology and accepted practices for cardiovascular imaging techniques to support authoritative recommendations for the use of imaging in client projects
  • Serve as lead subject matter expert internally and externally for the use of cardiovascular imaging technology in support of clinical trials, to educate clients or potential clients, and to establish awareness, drive collaboration and project efficiencies across service lines
  • Review study data for quality and integrity from a scientific perspective
  • Act as a scientific liaison to Clario personnel that are responsible for training and supporting imaging facilities participating in cardiovascular imaging across clinical trials
  • Support innovation and business development efforts

Secondary Responsibilities

Maintains Quality Service and Departmental Standards by:

  • Reading, understanding and adhering to organizational Standard Operating Procedures (“SOP”)
  • Assisting in establishing and enforcing departmental standards
  • Identify potential opportunities and risks within studies, including mitigations, and escalate to management as appropriate
  • Develop and apply problem solving strategies to address client issues, monitor progress, and ensure timely resolution to escalations
  • Influence strategic decision making and implement team objectives
  • Facilitate internal collaborations and communications by serving as a liaison between imaging and other product/service lines or departments

Maintains Technical And Industry Knowledge By

  • Attending and participating in applicable company-sponsored training
  • Supporting abstract and manuscript preparation
  • Conference attendance and presentation of abstracts

Contributes To Team Effort By

  • Working with internal staff to resolve issues
  • Exploring new opportunities to add value to organization and departmental processes
  • Helping others to achieve results
  • Performing other duties as assigned

Qualifications

Education:

  • PhD in biomedical engineering, cardiovascular imaging, biological science, or related field
  • A Master’s degree with extensive targeted cardiovascular imaging and clinical trial experience will be considered

Experience

  • 5+ years’ experience with at least one cardiovascular imaging modality, including advanced techniques
  • Working knowledge and solid understanding of clinical cardiac imaging physics and terminology across vendors
  • Proven ability in data processing and analysis for study reporting and publication
  • Proven ability in problem solving and critical thinking
  • Strong existing publication and abstract record
  • Existing knowledge of third party read systems (ex: Circle, MIM, Tomtec, Pie Medical) is a plus

Additional Skill Set

  • Ability to work in group setting and independently; ability to adjust to changing priorities
  • Excellent attention to detail and orientation toward meticulous work
  • Strong interpersonal and communication skills, both verbal and written
  • Strong documentation and organizational skills
  • Ability to project and maintain a professional and positive attitude
  • Knowledge and application of statistical analysis techniques
  • Development of presentation content and strong presentation skills
  • Ability to establish priorities, work independently, and proceed with objectives with minimal supervision in order to deliver high quality at high productivity

Working conditions

Travel: 0-20%

Lifting: 0-10 lbs.

Other: Computer work for long periods of time

This JOB description should not be deemed all-inclusive. Additional requirements and expectations may be assigned. At all times, employees are expected to adhere to company policies and company SOPs.

EEO Statement

Clario is an equal opportunity employer. Clario evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status, or any other legally protected characteristic.
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Additional Info
Min. Experience
-
Job Location
Remote
Job Type
Full-time
Job Seniority Level
Mid-Senior level
Job Duration
-
Language(s)
-
Est. Budget/Pay Rate
To be discussed
Est. hrs
-
Optimal Job Start
-
Job Industry
Biotechnology Research
Job Function
Research, Analyst, and Information Technology
Employer
Clario
Applicant Countries
United States,
Job Ref
J249FCB4A9A4F