Study Support Specialist I

Your New Company! At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! Whether you're a recent college graduate or seeking your next career opportunity, it's time to discover your future at Altasciences. We are better together and together We Are Altasciences. About The Role The Study Support Specialist will work with the Study Support teams to ensure the creation of study event designs and source. The Study Support Specialist will complete What You'll Do Here in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOP)s. What You'll Do Here

• Ensure the confidentiality of clinical trial volunteers and sponsors is respected.
• Maintain and advocate a high level of customer service and quality within the department.
• Understand protocol driven timed study events and acceptable collection windows (protocol and/or SOP driven) for the timed events.
• Review clinical trial protocols/manuals and SOPs to assess criteria that needs to be captured during clinical trial execution.
• Create and/or revise the study event design for staff scheduling.
• Ensure the review and approval of study event design, calendars and timelines are completed in a time efficient manner.
• Maintain various study event calendars for the clinical operations teams.
• Continuously update timeline workflows and programs.
• May create graphical report for Investigator review.
• Update and/or generate reports (i.e. flowsheets, meal logs).
• Maintain a continuous line of communication with clinical operations teams on the progression of clinical trial study events, source designs and timelines.
• Attend and/or participate in meetings (i.e. protocol, source design).
• Proactively communicate issues and/or problem resolutions to departmental supervisors and managers. What You'll Need to Succeed
• High School diploma or GED; college degree and related work
• Excellent written and verbal communication (French and English at the Montreal location)
• Leadership, interpersonal and organizational skills
• Customer service focused, able to work in a fast-paced environment What We Offer Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.

Altasciences' Benefits Package Includes:

Health/Dental/Vision Insurance Plans 401(k)/RRSP with

Employer Match Paid Vacation and Holidays Paid Sick and Bereavement Leave Employee Assistance & Telehealth Programs Altasciences' Incentive Programs Include:

Training & Development Programs Employee Referral Bonus Program Annual Performance Review #

LI-TN1 MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH

Altasciences is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability or any other protected grounds under applicable legislation. Reasonable accommodations for persons with disabilities during the recruitment process are available upon request. Join us at Altasciences!