Associate Project Lead

Ledger Run Inc.

Washington (District of Columbia)

Remote

USD 90,000 - 130,000

Full time

12 days ago

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Job summary

Ledger Run Inc. is seeking an Associate Project Lead to oversee global Investigator payments for assigned studies.

This remote role can be performed from anywhere in the United States, collaborating with clients and internal stakeholders to ensure timely, accurate payments in line with contracts and IRB requirements. The ideal candidate has a bachelor’s degree, 4 years in clinical trials, strong project management, and advanced Excel knowledge.

Qualifications

  • Bachelor’s degree or equivalent experience required.
  • 4 years of experience in clinical trials or related setting.
  • Strong project management and leadership skills.
  • Excellent verbal and written communication with clients.
  • Advanced knowledge of Microsoft Excel.
  • Proficient in Microsoft Word, SharePoint and Outlook.
  • Able to work independently and under pressure.
  • Good organizational and time-management abilities.
  • Basic understanding of budgeting and accounting recommended.

Responsibilities

  • Supervising daily operations and workload management for site payments.
  • Interact with clients and internal stakeholders to resolve issues.
  • Oversee payment processes in accordance with contracts and IRB requirements.
  • Review funding requests for trials.
  • QC of visit and invoiceable payment data.
  • Quarterly reconciliation of payment data during trials and closeout.
  • Manage escalations and client satisfaction.
  • Additional duties as assigned by team lead.

Skills

Project management
Leadership
Problem solving
Time management
Communication
Excel
Organizational skills
Independence
Attention to detail
Adaptability

Education

Bachelor’s degree
Equivalent experience

Tools

Microsoft Excel
Microsoft Word
SharePoint
Outlook

Job description

This is a remote role which can be performed from any location in the United States.

The Associate Project Lead is responsible for oversight of global Investigator payments for assigned studies. Responsibilities include managing client relationships, performing work to meet client commitments and collaboration with both internal and external stakeholders. The ideal candidate should possess experience within the biopharmaceutical industry and knowledge of budgets, contracts, investigator site payments and related activities.

QUALIFICATIONS & EXPERIENCE
  • Bachelor’s degree or equivalent experience required
  • 4 years of experience in clinical trials or related setting required
  • Strong project management and leadership skills required
  • Requires problem-solving and time management skills
  • Must possess excellent verbal and written communication skills and communicate professionally with clients
  • Must have advanced knowledge of Microsoft Excel
  • Must be proficient in Microsoft Word, SharePoint and Outlook
  • Must have excellent organizational skills
  • Must be able to learn quickly, be comfortable with new technology systems and adapt to system changes
  • Capable of working independently and being proactive in a team
  • Demonstrates proficiency in performing under pressure and meeting deadlines efficiently
  • Ability to proof-read and detect errors in math, and grammar
  • A proficient understanding of basic accounting and budgeting is recommended
DUTIES & RESPONSIBILITIES
  • Supervising and managing daily operations and workloads, including but not limited to reviewing site payments, conducting client meetings, and overseeing study funds management
  • Interacts and collaborates with clients and internal stakeholders to enhance experience, address queries, and resolve issues
  • Oversee and manage all aspects of payments relating to clinical trials to ensure timely and accurate payment processes in accordance with agreements, IRB, and/or ethics committee requirements
  • Review and manage funding requests for clinical trials
  • Perform primary QC of visit and invoiceable payment data
  • Perform quarterly reconciliation review of payment data during the life of the clinical trial and during closeout
  • Manage project escalations to identify the root cause of issues and resolve to clients’ satisfaction
  • Other duties as required and assigned by designated team lead. These may, on occasion, be unrelated to the position described here.
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