Study Manager
Kelly Science and Clinical FSP is currently seeking a Study Manager for a long-term engagement with one of our Global Pharmaceutical clients. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly Services, Inc. This role is full-time and is offering full benefit options. As a Kelly FSP employee you may be eligible for Medical, Dental, Vision, 401K (no match) and a variety of other benefits to choose from. You may also be eligible for paid time off, including holiday, vacation, and sick/personal time.
Description Of Services
⢠Assists the SM Study Lead and study team with the operational conduct of clinical studies (e.g., CTT minutes, clinical supplies planning/tracking, lab specimen tracking, imaging data reconciliation, status update reports, study closeout activities)
⢠May support a single study or multiple studies
⢠May lead a study with limited scope (e.g., Survival Follow-up)
⢠May be responsible for tracking study timelines and will be proficient in project management tools
⢠May interact with internal and external stakeholders (study sites, vendors, committees, etc.) in support of clinical study objectives
Minimum Years of Experience
⢠At least 2 year Pharmaceutical and/or clinical drug development experience (such as pharmaceutical/biopharma companies, hospital settings, research sites, clinical trial units, CRO, SMO) in the last 5 years required
⢠TA-specific experience beneficial
⢠Demonstrated oral and written communication skills
⢠Proficiency in Microsoft Office (Outlook, Word, Excel and PowerPoint) required; OneNote experience preferred.
Educational Requirements
⢠BS/BA/MS/PhD
Applicants must be currently authorized to work in the US on a full-time basis now and in the future.
Fraudulent Applications: All information provided during the application process will be verified. Misrepresentation of credentials, identity fraud, or use of proxy interviewers will result in immediate disqualification and may be reported to appropriate authorities.
Posted By: Karli Minor
Apply Now
Apply Now
Description Of Services
⢠Assists the SM Study Lead and study team with the operational conduct of clinical studies (e.g., CTT minutes, clinical supplies planning/tracking, lab specimen tracking, imaging data reconciliation, status update reports, study closeout activities)
⢠May support a single study or multiple studies
⢠May lead a study with limited scope (e.g., Survival Follow-up)
⢠May be responsible for tracking study timelines and will be proficient in project management tools
⢠May interact with internal and external stakeholders (study sites, vendors, committees, etc.) in support of clinical study objectives
Minimum Years of Experience
⢠At least 2 year Pharmaceutical and/or clinical drug development experience (such as pharmaceutical/biopharma companies, hospital settings, research sites, clinical trial units, CRO, SMO) in the last 5 years required
⢠TA-specific experience beneficial
⢠Demonstrated oral and written communication skills
⢠Proficiency in Microsoft Office (Outlook, Word, Excel and PowerPoint) required; OneNote experience preferred.
Educational Requirements
⢠BS/BA/MS/PhD
Applicants must be currently authorized to work in the US on a full-time basis now and in the future.
Fraudulent Applications: All information provided during the application process will be verified. Misrepresentation of credentials, identity fraud, or use of proxy interviewers will result in immediate disqualification and may be reported to appropriate authorities.
Posted By: Karli Minor
Apply Now
Apply Now