Project Manager - Clinical Market Research
New
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SagoMarket Research, Clinical
United StatesFull-TimeMiddle
Salary not disclosed
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Job Details
- Experience
- 4+ years
- Required Skills
- GCPMicrosoft ExcelMicrosoft Office
Requirements
- Minimum of 4+ years in a market research or clinical environment
- Strong knowledge of clinical practices
- Bachelor’s degree (Master’s preferred)
- Excellent oral and written communication skills
- Strong interpersonal abilities
- Highest level of professionalism
- Ability to effectively engage respondents and secure their cooperation
- Strong client service orientation
- In-depth knowledge of clinical research practices
- Advanced industry knowledge in clinical research and data collection
- Deep understanding of departmental roles, processes, and functions
- Adaptable, with ability to work independently and collaboratively
- Proven ability to multitask and thrive in a fast-paced environment
- Proficiency in Microsoft Office
- Proficiency in Excel
Responsibilities
- Manage all aspects of Clinical market research projects accurately with internal/external clients
- Determine business/project problems and establish project objectives
- Analyze and oversee data collection for clinical surveys
- Maintain close contact with the client, ensuring they are aware of project status and addressing changes
- Complete all required trainings and certifications (e.g., GCP, CITI)
- Understand, implement, and ensure project execution according to study protocol and Sago’s Quality Management System Standards
- Manage quality of work for projects, including development and review of study materials and project schedule
- Attend project update meetings, lead study briefings, and work with Call Center on recruitment
- Maintain quota control and validate work according to guidelines
- Maintain positive subject/respondent relationships to support ongoing participation
- Complete required reporting and inform the Clinical team of project issues
- Manage subject/respondent in accordance with project specifications
- Execute trainings as identified in the protocol
- Utilize Sago’s Clinical data management and reporting systems
- Execute Participant Interviews via phone or in person
- Travel to assigned destinations for clinical research study, client meetings, or trainings
- Assist in writing Protocols, working with the sponsor, and submitting documents to the IRB
- Perform site certifications and site audits
- Deliver client-ready deliverables such as cross tabs, Excel files, prescreening data
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