Study Coordinator
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
Works under the guidance of designated Study Director(s), Contributing Scientists and Principal
Investigators, as appropriate, to provide administrative and professional support for accurate
study progression based on Protocols and Method Validation Plans, organization, scheduling,
reporting, client relations and operations.
What You’ll Do Here
- Assist with the preparation and distribution of Protocols, Analytical Study Plans and
Amendments/Amended Protocols. - Schedule and/or help conduct Protocol review meetings with Study Director guidance.
- Create study schedules for data collection within the electronic data capture system and
implement schedule changes as a result of Protocol Amendments/Amended Protocols, as
necessary. - Draft and edit Project Review Forms (PRF) with Study Director guidance.
- Assist with preparation and maintenance of study notebooks, study forms, and other
necessary materials for studies. - Support the Study Director or Principal Investigator with the planning and hosting of client
visits. - Review raw data throughout the life of a study for clerical/technical errors, thoroughness
and consistency, and adherence to SOPs, Protocol specifications and compliance with Good Laboratory Practices (GLPs), as appropriate. Coordinate correction of raw data with
appropriate staff. Report any deviations to the Study Director. - Coordinate study activities related to audits.
- Perform data verification as needed.
- Assist in the preparation of the report(s) (e.g. drafting the Materials and Methods section), utilizing the appropriate report template.
- Collect and collate report components for the final report under the supervision of the
- Study Director utilizing electronic publishing tools.
- Provide assistance with archiving and preparation of studies for finalization.
- Support the Study Director(s), Contributing Scientists and Principal Investigators with the monitoring, tracking and communication of study milestones throughout departments.
- Provide coordination for both non-GLP studies and GLP studies from study initiation to finalization under the guidance of the Study Director.
- Generate data tables for inclusion in reports based on requirements of the study.
What You’ll Need to Succeed
- A bachelors degree or college coursework in a scientific discipline and relevant experience may substitute for the educational requirement.
- 0 -1 years experience in a scientific environment or an equivalent combination of education and experience.
- General to advanced computer skills, including proficiency with Microsoft Word and Excel.
- Working knowledge of descriptive statistics.
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
- Telework when applicable
- Training & Development Programs
- Employee Referral Bonus
Other details
- Job Family T-3
- Pay Type Hourly
- Everett, WA, USA