What are the responsibilities and job description for the Clinical Science Associate position at Clario?
Overview
As a member of a team of accomplished scientists, clinicians, and data analysts, the Clinical Science Associate supports the Clinical Science & Consulting team in a software company that creates electronic data collection systems for clinical trials. This team supports and drives the sales and delivery of Clario services by providing scientific guidance and analysis to the Sales, Marketing, and Client Services functions. The Clinical Science Associate is responsible for managing multiple Clinical Science operational and analytical support functions and coordinating delivery of the highest quality consulting services.
Clario. The Best of ERT & Bioclinica!
Clario delivers the leading endpoint technology solutions for clinical trials. Through experience gained from over 19,000 clinical trials delivered in support of 870 regulatory approvals, Clario fuses scientific expertise and global scale into the broadest endpoint technology platform to enable pharmaceutical, biotech and medical device partners to transform lives. Through Trial Anywhere™, Clario has mastered the ability to generate rich evidence across all trial models: decentralized, hybrid and site-based clinical trials. With 30 facilities in nine countries across North America, Europe and Asia Pacific, Clario’s global team of science, technology and operational experts has been delivering the richest clinical evidence for nearly 50 years.
Responsibilities
Clinical Science & Consulting (CSC) Core Duties:
Sales Support:
Study Support & Client Services Coordination:
Marketing Support:
Acquire and maintain critical knowledge to support sales and Clario project teams
Work Conditions:
The duties and responsibilities listed in this job description represent the major responsibilities of the position. Other duties and responsibilities may be assigned, as required. This job description and any attachments do not constitute or represent a contract.
#LI-DNI
Qualifications
Education:
- Master’s degree with a focus in research methodology, data analysis, or statistics (e.g., MPH, MBA, MHA) or Bachelor’s degree with demonstrated equivalent experience
Experience:
- Minimum of three years of experience in the execution of clinical trials, drug development life cycle and/or health care software implementation or equivalent (minimum of 5 years for candidates without a Master’s degree)
- Experience in eCOA, Respiratory, Cardiac, Precision Motion (wearables/sensors) preferred
- Proven experience in clinical research methodologies and/or data management
- Familiarity with FDA regulatory processes and clinical research processes
- Experienced and comfortable with project management software, developing presentations, and delivering presentations
- Excellent knowledge of Microsoft® Office and SPSS required; experience with data visualization software and Python a plus.
- Business driven and business growth savvy.
- Comfortable and fearless learning new roles, versatile, fast learner
- Team leader & team player; must be a self-starter and able to function in a high-paced,
dynamic environment.
- Excellent interpersonal and communication skills; Ability to understand and communicate with representatives from the range of disciplines within biopharmaceutical development
- Ability to manage multiple priorities and projects, and balance workload and timelines; Able to work in a fast-paced and dynamic environment
Clario is an equal opportunity employer and all qualified applicants receive consideration for employment without regard characteristic to race, color, religion, sex, national origin, disability status, protected veteran status, or any other protected by law.
