Project Manager
at Scout
Remote, Scotland, United Kingdom -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 29 Oct, 2024 | GBP 65000 Annual | 29 Jul, 2024 | N/A | Good communication skills | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
Established in 1996 and rebranded to Scout in 2024, we built our foundation on planning meetings for numerous organizations within the life sciences sector (Scout Meetings). In response to emerging industry needs, we expanded our services to include Scout Clinical, one of the top providers of clinical trial patient travel and reimbursements, and Scout Academy, our secure, online, on-demand learning management system that ensures global compliance.
Scout is recognized as a leader in our field for innovation in service, attention to detail, our stellar team members, and making the complex easier. If this interests you, we’d love to have you join our rapidly growing team!
POSITION SUMMARY:
We are looking to hire a talented and eager Project Manager to join our UK team in a remote position. The Project Manager will perform a wide variety of activities to support the start-up, management, and completion of patient services for clinical research studies. They will report directly to Director, of Project Management and will manage sponsors and vendors, and deliver project activities on time. This position is work from home and no travel.
THE IDEAL CANDIDATE WILL HAVE THE FOLLOWING EXPERIENCE, SKILLS, AND KNOWLEDGE:
- Strong understanding of project management
- Strong understanding of the clinical trial process and clinical trial protocols
- Ability to handle multiple projects in various planning stages concurrently
- Ability to track and manage key dates/deadlines
Responsibilities:
- Contracts support; review protocols in support of new requests for proposal
- Study management activities and study start-up
- Maintain activities spreadsheet for studies
- Regular communication with global study stakeholders including CRO and Sponsors
- Schedule and conduct study on-boarding phone calls, KOMs, IMs and follow-up calls
- Act as main point of contact to Sponsor and CRO clients for Scout Clinical services for assigned studies
- Collaborate on operational internal policies and manage adherence
- Oversee regulatory onboarding process of studies in collaboration with Scout Clinical Compliance Team
- Provide study-specific patient and site-facing documentation
- Ongoing administrative tasks/document management throughout life of the study
- Oversee training of sites, patients, and study teams on utilization of the Scout Clinical portal in collaboration with the Scout Clinical Trial Manager
- Oversee and manage Scout Clinical portal configuration for assigned studies
- Work with Patient Liaison team to support travel and reimbursement activities associated with assigned studies
- Liaise with Finance to produce statements, reports, and invoices and confirm monthly submissions to clients for assigned studies
- Serve as an additional Subject Matter Expert for Scout software development team
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
Remote, United Kingdom