Study Support Specialist I

Posted 2 Hours Ago
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Overland Park, KS, USA
In-Office
Entry level
Information Technology • Analytics • Biotech
The Role
The Study Support Specialist assists with study event designs, maintains study calendars, ensures compliance with protocols, and communicates with clinical teams.
Summary Generated by Built In

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!

Top Skills

Good Clinical Practices
Graphical Reporting Tools
MS Office
Standard Operating Procedures
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The Company
HQ: Laval, Quebec
1,832 Employees
Year Founded: 1995

What We Do

Outsourcing made easy with a one-stop solution to early-phase drug development. We are an integrated drug development solution company, offering pharmaceutical and biotechnology companies a proven, flexible approach that removes the need for multiple service providers during the early stages of drug development. Whether for one study or an end-to-end program, we help you reach critical decision-making milestones sooner by improving speed and ease from lead candidate selection to clinical proof of concept, and beyond. When partnering with Altasciences, you can experience up to 40% in time savings thanks to our integrated, one-stop solution offering. We strive to create a true partnership with our clients, our partners, and our colleagues that enables a mutually supporting relationship built on a combination of excellent science and solid communication. Helping sponsors get better drugs to the people who need them, faster, for over 25 years. Our full-service offering is always tailored to your specific research needs: - Preclinical research - Clinical pharmacology - Drug formulation - Manufacturing and analytical services - Bioanalysis - Program management - Medical writing - Biostatics - Data management - And so much more!

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