Altasciences
Study Coordinator I
Altasciences, Columbia, Missouri, United States, 65201
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 RoleWorks under the guidance of designated Study Director(s), Contributing Scientists and PrincipalInvestigators, as appropriate, to provide administrative and professional support for accuratestudy progression based on Protocols and Method Validation Plans, organization, scheduling,reporting, client relations and operations.
What You'll Do HereAssist 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.Generate data tables for inclusion in reports based on requirementsAssist 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.
What You'll Need to SucceedA Bachelor degree or college coursework in a scientific discipline and relevant experience may substitute for the educational requirement.A minimum of 1 year experience in a scientific environment or an equivalent combination of education and experience.General to advanced computer skills: proficiency working with MS Word, Excel and Adobe Acrobat.Excellent verbal and written communication skills.Working knowledge of descriptive statistics.
What We OfferAltasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.
Altasciences' Benefits Package IncludesHealth/Dental/Vision Insurance Plans401(k)/RRSP with Employer MatchPaid Vacation and HolidaysPaid Sick and Bereavement LeaveEmployee Assistance & Telehealth ProgramsTelework when applicable
Altasciences' Incentive Programs IncludeTraining & Development ProgramsEmployee Referral Bonus
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!
We are better together and together We Are Altasciences.
About The RoleWorks under the guidance of designated Study Director(s), Contributing Scientists and PrincipalInvestigators, as appropriate, to provide administrative and professional support for accuratestudy progression based on Protocols and Method Validation Plans, organization, scheduling,reporting, client relations and operations.
What You'll Do HereAssist 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.Generate data tables for inclusion in reports based on requirementsAssist 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.
What You'll Need to SucceedA Bachelor degree or college coursework in a scientific discipline and relevant experience may substitute for the educational requirement.A minimum of 1 year experience in a scientific environment or an equivalent combination of education and experience.General to advanced computer skills: proficiency working with MS Word, Excel and Adobe Acrobat.Excellent verbal and written communication skills.Working knowledge of descriptive statistics.
What We OfferAltasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.
Altasciences' Benefits Package IncludesHealth/Dental/Vision Insurance Plans401(k)/RRSP with Employer MatchPaid Vacation and HolidaysPaid Sick and Bereavement LeaveEmployee Assistance & Telehealth ProgramsTelework when applicable
Altasciences' Incentive Programs IncludeTraining & Development ProgramsEmployee Referral Bonus
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!