AmplifyBio
Study Coordinator
AmplifyBio, West Jefferson, Ohio, United States, 43162
Are you passionate about significantly improving the future of medicine? Do you believe that people are the most important asset of any company? If so, join
AmplifyBio !
Amplify
Bio
is a leading contract research organization with a comprehensive range of services that span from being an outsourcing partner for discovery stage R&D work, a preclinical CRO performing safety efficacy and toxicology studies for small molecules and advanced therapies alike, and, most recently, an expansion into manufacturing services for cell, gene, and mRNA-based therapeutics.
The
Amplify
Bio
ecosystem is comprised of three distinct business units:
ADOC
(South San Francisco, CA)- Amplify's Discovery, Optimization, and Characterization laboratories:
ASET
(West Jefferson, OH) - Amplify's Safety, Efficacy, and Toxicology Site; and the most recently opened
AMEC
(New Albany, OH) - Amplify's Manufacturing Enablement Center.
About
ASET
West Jefferson, OH :
AmplifyBio's
safety, efficacy, and toxicology unit (ASET) was launched as a preclinical CRO that spun out of Battelle in 2021 to address the changing needs of commercial organizations developing modern therapeutics. AmplifyBio brings decades of experience to accommodate a wide variety of GLP and non-GLP studies in all in vivo models and dose routes. Among the investments that AmplifyBio has made to empower preclinical assessments of advanced therapies is building a new state-of-the-art analytical laboratory to include molecular and immunological assays that assess critical safety and efficacy indicators for cell and gene therapies during preclinical studies
AmplifyBio
is currently looking to hire a
Study Coordinator
to join our growing Study Management team!!!
The
Study Coordinator
is responsible for assisting the Study Director with all aspects of the study, including overseeing pre-study, in-life, and reporting phases of a study. This position will join a staff of highly trained scientist and technicians, and state of the art facilities to support our clients' toxicology, safety pharmacology, and inhalation research programs. AmplifyBio is rapidly expanding its service offerings related to the discovery, translation, and development of advanced therapies such as gene and cell therapies.
As part of
AmplifyBio's
Study Management team, the right candidate will help support the company's growing portfolio of service offerings and commercial capabilities. This is a unique opportunity to be part of an emerging startup bringing innovative technology to advanced therapies.
What You'll Do Here:
Add study information to Electronic Database and keep up to date.Assist with protocol/amendment development, timeline creation, and IACUC submission.Study start preparation, including animal requests, request for equipment, generating study distribution list, Provantis protocol set up and table generation, study calendar review, and scheduling pre-study meetings.Prepare study specific in-life forms, labels, and memos.Attend critical in-life events as needed.Prepare deviations according to SOP.Notify Master scheduler of study phase changes.Assist with responses to QAU audits.Monitor report timelines, assist with report generation, and perform report QC.Assist in the preparation of study files for archiving per SOP, GLP and client specifications.Mentor and train junior staff in Study Coordinator duties.We Would Love to Hear from You If:
Bachelor's Degree: Equivalent combination of education, training, and experience may be substituted for degree.Knowledge of GLP regulations and guidelines; basic quality review techniques.Strong interpersonal skills.Excellent problem-solving skills.Effective organization, communication, and team orientation skills.Ability to initiate assigned tasks, to work independently, and manage time.Ability to manage multiple projects.Ability to establish and maintain effective working relationships with coworkers, managers, and clients.Must be willing to work in a biosafety level 2 (BSL2) and/or 3 (BSL3) environment and able to wear appropriate respiratory protection.Desired Skills:
Experience using the Provantis Data capture system to set up protocols, generate tables, input, and review data.Experience reviewing in-vivo and in-vitro data including, but not limited to, inhalation, pathology, chemistry, PCR, and ELISA.Experience with Microsoft software (WORD, EXCEL, PowerPoint).At
AmplifyBio , we're committed to growing and empowering an inclusive community within our company and industry. This is why we hire and cultivate diverse teams of the best and brightest from all backgrounds, experiences, and perspectives across our organization.
AmplifyBio
is an equal opportunity employer, and we value diversity at our company. We don't discriminate on the basis of race, color, citizenship status, national origin, ancestry, gender (including gender expression and gender identity), sexual orientation, age, weight, religion, creed, physical or mental disability, marital status, veteran status, political affiliation, or any other factor protected by federal, state, or local law.
Why You Will Love Working Here:
We take the health and happiness of our employees seriously and consistently evaluate new ways to Amp up our benefits to provide an amazing place to work. From a wellness program (did we mention we have an onsite gym with state-of-the-art equipment and ping pong table?), to financial planning and legal assistance, we make sure to take care of our own.
Health, Dental, and Vision insurance that starts on your first day at
AmplifyBio!Competitive Compensation PackageWe take work-life balance seriously and we back it up with a FLEXIBLE PTO policy!Generous paid parental leaveWellness and Self-Care Programs401(k) matchTuition ReimbursementEAP/work-life support systemA fun work environment where everyone's voice matters!We are just getting started! More benefits on the way!An Opportunity to Change the World!!!
When you join our team , you will be a part of groundbreaking work while collaborating with our clients, research scientists, study directors, lab technicians, and specialists across a variety of disciplines. The future for
AmplifyBio
is as great as the combination of our imaginations and actions, and we hold ourselves accountable for our choices and results. We have a bias for action, excellence, and, especially, the health and safety of our employees.
AmplifyBio !
Amplify
Bio
is a leading contract research organization with a comprehensive range of services that span from being an outsourcing partner for discovery stage R&D work, a preclinical CRO performing safety efficacy and toxicology studies for small molecules and advanced therapies alike, and, most recently, an expansion into manufacturing services for cell, gene, and mRNA-based therapeutics.
The
Amplify
Bio
ecosystem is comprised of three distinct business units:
ADOC
(South San Francisco, CA)- Amplify's Discovery, Optimization, and Characterization laboratories:
ASET
(West Jefferson, OH) - Amplify's Safety, Efficacy, and Toxicology Site; and the most recently opened
AMEC
(New Albany, OH) - Amplify's Manufacturing Enablement Center.
About
ASET
West Jefferson, OH :
AmplifyBio's
safety, efficacy, and toxicology unit (ASET) was launched as a preclinical CRO that spun out of Battelle in 2021 to address the changing needs of commercial organizations developing modern therapeutics. AmplifyBio brings decades of experience to accommodate a wide variety of GLP and non-GLP studies in all in vivo models and dose routes. Among the investments that AmplifyBio has made to empower preclinical assessments of advanced therapies is building a new state-of-the-art analytical laboratory to include molecular and immunological assays that assess critical safety and efficacy indicators for cell and gene therapies during preclinical studies
AmplifyBio
is currently looking to hire a
Study Coordinator
to join our growing Study Management team!!!
The
Study Coordinator
is responsible for assisting the Study Director with all aspects of the study, including overseeing pre-study, in-life, and reporting phases of a study. This position will join a staff of highly trained scientist and technicians, and state of the art facilities to support our clients' toxicology, safety pharmacology, and inhalation research programs. AmplifyBio is rapidly expanding its service offerings related to the discovery, translation, and development of advanced therapies such as gene and cell therapies.
As part of
AmplifyBio's
Study Management team, the right candidate will help support the company's growing portfolio of service offerings and commercial capabilities. This is a unique opportunity to be part of an emerging startup bringing innovative technology to advanced therapies.
What You'll Do Here:
Add study information to Electronic Database and keep up to date.Assist with protocol/amendment development, timeline creation, and IACUC submission.Study start preparation, including animal requests, request for equipment, generating study distribution list, Provantis protocol set up and table generation, study calendar review, and scheduling pre-study meetings.Prepare study specific in-life forms, labels, and memos.Attend critical in-life events as needed.Prepare deviations according to SOP.Notify Master scheduler of study phase changes.Assist with responses to QAU audits.Monitor report timelines, assist with report generation, and perform report QC.Assist in the preparation of study files for archiving per SOP, GLP and client specifications.Mentor and train junior staff in Study Coordinator duties.We Would Love to Hear from You If:
Bachelor's Degree: Equivalent combination of education, training, and experience may be substituted for degree.Knowledge of GLP regulations and guidelines; basic quality review techniques.Strong interpersonal skills.Excellent problem-solving skills.Effective organization, communication, and team orientation skills.Ability to initiate assigned tasks, to work independently, and manage time.Ability to manage multiple projects.Ability to establish and maintain effective working relationships with coworkers, managers, and clients.Must be willing to work in a biosafety level 2 (BSL2) and/or 3 (BSL3) environment and able to wear appropriate respiratory protection.Desired Skills:
Experience using the Provantis Data capture system to set up protocols, generate tables, input, and review data.Experience reviewing in-vivo and in-vitro data including, but not limited to, inhalation, pathology, chemistry, PCR, and ELISA.Experience with Microsoft software (WORD, EXCEL, PowerPoint).At
AmplifyBio , we're committed to growing and empowering an inclusive community within our company and industry. This is why we hire and cultivate diverse teams of the best and brightest from all backgrounds, experiences, and perspectives across our organization.
AmplifyBio
is an equal opportunity employer, and we value diversity at our company. We don't discriminate on the basis of race, color, citizenship status, national origin, ancestry, gender (including gender expression and gender identity), sexual orientation, age, weight, religion, creed, physical or mental disability, marital status, veteran status, political affiliation, or any other factor protected by federal, state, or local law.
Why You Will Love Working Here:
We take the health and happiness of our employees seriously and consistently evaluate new ways to Amp up our benefits to provide an amazing place to work. From a wellness program (did we mention we have an onsite gym with state-of-the-art equipment and ping pong table?), to financial planning and legal assistance, we make sure to take care of our own.
Health, Dental, and Vision insurance that starts on your first day at
AmplifyBio!Competitive Compensation PackageWe take work-life balance seriously and we back it up with a FLEXIBLE PTO policy!Generous paid parental leaveWellness and Self-Care Programs401(k) matchTuition ReimbursementEAP/work-life support systemA fun work environment where everyone's voice matters!We are just getting started! More benefits on the way!An Opportunity to Change the World!!!
When you join our team , you will be a part of groundbreaking work while collaborating with our clients, research scientists, study directors, lab technicians, and specialists across a variety of disciplines. The future for
AmplifyBio
is as great as the combination of our imaginations and actions, and we hold ourselves accountable for our choices and results. We have a bias for action, excellence, and, especially, the health and safety of our employees.