Clinical Research Budget Analyst

  • location: Cary, NC
  • type: Permanent
  • salary: $50,000 - $60,000 per year
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job description

Clinical Research Budget Analyst

job summary:
SUMMARY OF POSITION:

The Payments Analyst is responsible for managing study specific, global site payment processes for clinical trials.

QUALIFICATIONS/EXPERIENCE:

  • Minimum of 1 to 4 years' experience in clinical trial setting and/or pharmaceutical industry a plus.
  • Experience negotiating investigator contracts and budgets.
  • Must be comfortable analyzing large data sets.
  • Demonstrated knowledge of clinical research terminology.
  • Must have advanced knowledge of Microsoft Excel, Word, Outlook and Access.
  • Attention to detail required in a highly regulated industry.
  • Ability to work independently, and be a pro-active team player is required.
  • Must possess excellent verbal and written communication skills.
  • Ability to communicate with international contacts accurately and professionally will be required.
  • Ability to proof-read and detect errors in typing, spelling, grammar, syntax and punctuation required.
  • Ability to handle multiple tasks to meet deadlines in a dynamic environment required.
ESSENTIAL DUTIES/RESPONSIBILITIES:

To perform this job successfully, an individual must be able to perform each essential duty and responsibility satisfactorily. The requirements listed below are representative of the knowledge, skills, and/or ability required.

  • Manage study specific, global site payment processes.
  • Ability to decipher necessary information from sponsor specific documents including budgets and payment terms in contracts, amendments, and ancillary agreements.
  • Create and distribute pro forma globally where required.
  • Respond to inquiries from sites and sponsors efficiently and effectively.
  • Follow-up with investigative sites to resolve any payment issues globally.
  • Produce error-free reports for sponsors and internal project teams.
  • Accurately plan to achieve timeline milestones and deadlines.
 
location: Cary, North Carolina
job type: Permanent
salary: $50,000 - 60,000 per year
work hours: 8 to 5
education: No Degree Required
experience: 3 Years
 
responsibilities:
To perform this job successfully, an individual must be able to perform each essential duty and responsibility satisfactorily. The requirements listed below are representative of the knowledge, skills, and/or ability required.

  • Manage study specific, global site payment processes.
  • Ability to decipher necessary information from sponsor specific documents including budgets and payment terms in contracts, amendments, and ancillary agreements.
  • Create and distribute pro forma globally where required.
  • Respond to inquiries from sites and sponsors efficiently and effectively.
  • Follow-up with investigative sites to resolve any payment issues globally.
  • Produce error-free reports for sponsors and internal project teams.
  • Accurately plan to achieve timeline milestones and deadlines.
 
qualifications:
  • Minimum of 1 to 4 years' experience in clinical trial setting and/or pharmaceutical industry a plus.
  • Experience negotiating investigator contracts and budgets.
  • Must be comfortable analyzing large data sets.
  • Demonstrated knowledge of clinical research terminology.
  • Must have advanced knowledge of Microsoft Excel, Word, Outlook and Access.
  • Attention to detail required in a highly regulated industry.
  • Ability to work independently, and be a pro-active team player is required.
  • Must possess excellent verbal and written communication skills.
  • Ability to communicate with international contacts accurately and professionally will be required.
  • Ability to proof-read and detect errors in typing, spelling, grammar, syntax and punctuation required.
  • Ability to handle multiple tasks to meet deadlines in a dynamic environment required.
 
skills: Contract Administration, A/P Processing
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

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