Study Start Up Associate I
Behavioral Health Market Context
Apply Nowvia ICON Plc
Benefits
Health Insurance
Job Description
join ICON’s Medical Imaging & Cardiac Safety Solutions Site Management team. The Study Start Up Associate I is responsible for assigned project site start-up and qualification activities per study specific requirements. They will provide support to sites for the life of all assigned projects. The Study Start Up Associate I may carry a mixed portfolio of Imaging and Cardiac studies of varying complexity.
Location: Office Based Hybrid (average of 3 days per week)
• Rochester, NY
• Blue Bell, PA
What you will be doing:
• Establishing and maintaining strong working relationships with site contacts and internal departments
• Serving as main point of contact for Imaging and/or Cardiac sites participating in Clinical Trials
• Providing site support via email and telephone
• Generating and documenting all site communications associated with the Site Qualification process from initial contact to First Participant Ready status
• Providing sites their necessary access credentials
• Maintaining an audit ready file documenting the qualification process for all sites
• Ensuring weekly status follow ups are completed on time and entered in the site database
• Entering and updating site information in the site database as needed throughout the study
• Maintaining study specific site qualification trackers for sponsors
• Providing support and site updates on internal/external Kick Off meetings and weekly teleconferences
• Collaboration with Documentation & Training to ensure study requirements are in alignment and communicated with sites accordingly
• Request/track sites return equipment at study close
• Providing daily and weekly metrics for completed activities to management
• Creating unique project specific templates for site communication
• Proactively communicating with Project Management if issues or concerns arise that may impact site qualification
• Managing special projects and programs assigned by the Manager, Site Operations
Your profile:
• 1-2+ years of administrative and customer/client service experience in a professional setting, preferably in clinical research
• Advanced Microsoft Office Suite skills, specifically with Outlook and Excel
• Strong attention to detail and organizational skills
• Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams
• Ability to work independently and manage multiple tasks simultaneously in a fast-paced environment
• Associates degree in business, life sciences, or a related field
#LI-TP1
#LI-Hybrid
What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
Salary range: $51,552.00-$64,440.00
Bonus, Com, Stock, Benefits & Disclaimer verbiage:
Actual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill level. You may be eligible for a bonus, stock compensation and commissions in some cases depending on your role and performance.
Are you a current ICON Employee? Please click here to apply
Location: Office Based Hybrid (average of 3 days per week)
• Rochester, NY
• Blue Bell, PA
What you will be doing:
• Establishing and maintaining strong working relationships with site contacts and internal departments
• Serving as main point of contact for Imaging and/or Cardiac sites participating in Clinical Trials
• Providing site support via email and telephone
• Generating and documenting all site communications associated with the Site Qualification process from initial contact to First Participant Ready status
• Providing sites their necessary access credentials
• Maintaining an audit ready file documenting the qualification process for all sites
• Ensuring weekly status follow ups are completed on time and entered in the site database
• Entering and updating site information in the site database as needed throughout the study
• Maintaining study specific site qualification trackers for sponsors
• Providing support and site updates on internal/external Kick Off meetings and weekly teleconferences
• Collaboration with Documentation & Training to ensure study requirements are in alignment and communicated with sites accordingly
• Request/track sites return equipment at study close
• Providing daily and weekly metrics for completed activities to management
• Creating unique project specific templates for site communication
• Proactively communicating with Project Management if issues or concerns arise that may impact site qualification
• Managing special projects and programs assigned by the Manager, Site Operations
Your profile:
• 1-2+ years of administrative and customer/client service experience in a professional setting, preferably in clinical research
• Advanced Microsoft Office Suite skills, specifically with Outlook and Excel
• Strong attention to detail and organizational skills
• Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams
• Ability to work independently and manage multiple tasks simultaneously in a fast-paced environment
• Associates degree in business, life sciences, or a related field
#LI-TP1
#LI-Hybrid
What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
Salary range: $51,552.00-$64,440.00
Bonus, Com, Stock, Benefits & Disclaimer verbiage:
Actual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill level. You may be eligible for a bonus, stock compensation and commissions in some cases depending on your role and performance.
Are you a current ICON Employee? Please click here to apply
Qualifications
- •1-2+ years of administrative and customer/client service experience in a professional setting, preferably in clinical research
- •Advanced Microsoft Office Suite skills, specifically with Outlook and Excel
- •Strong attention to detail and organizational skills
- •Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams
- •Ability to work independently and manage multiple tasks simultaneously in a fast-paced environment
- •Associates degree in business, life sciences, or a related field
Benefits
- •In addition to your competitive salary, ICON offers a range of additional benefits
- •Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family
- •Various annual leave entitlements
- •A range of health insurance offerings to suit you and your family’s needs
- •Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
- •Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
- •Life assurance
- •Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others
- •Salary range: $51,552.00-$64,440.00
- •Actual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill level
- •You may be eligible for a bonus, stock compensation and commissions in some cases depending on your role and performance
Responsibilities
- •The Study Start Up Associate I is responsible for assigned project site start-up and qualification activities per study specific requirements
- •They will provide support to sites for the life of all assigned projects
- •The Study Start Up Associate I may carry a mixed portfolio of Imaging and Cardiac studies of varying complexity
- •Establishing and maintaining strong working relationships with site contacts and internal departments
- •Serving as main point of contact for Imaging and/or Cardiac sites participating in Clinical Trials
- •Providing site support via email and telephone
- •Generating and documenting all site communications associated with the Site Qualification process from initial contact to First Participant Ready status
- •Providing sites their necessary access credentials
- •Maintaining an audit ready file documenting the qualification process for all sites
- •Ensuring weekly status follow ups are completed on time and entered in the site database
- •Entering and updating site information in the site database as needed throughout the study
- •Maintaining study specific site qualification trackers for sponsors
- •Providing support and site updates on internal/external Kick Off meetings and weekly teleconferences
- •Collaboration with Documentation & Training to ensure study requirements are in alignment and communicated with sites accordingly
- •Request/track sites return equipment at study close
- •Providing daily and weekly metrics for completed activities to management
- •Creating unique project specific templates for site communication
- •Proactively communicating with Project Management if issues or concerns arise that may impact site qualification
- •Managing special projects and programs assigned by the Manager, Site Operations
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