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Investigator Grants Specialist - EUROPE - Remote

Employer
Worldwide Clinical Trials
Location
United Kingdom
Salary
Competitive
Start date
8 Dec 2021
Closing date
7 Jan 2022

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Discipline
Clinical Research, Clinical Operations
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details

SUMMARY: The Investigator Grants Specialist is responsible for the development and dissemination of Investigator Grants (pre and post-award) while supporting various groups related to Investigator Grants delivery .

RESPONSIBILITIES:
  • Reports directly to the Investigator Grants Manager.
  • Responsible for the development, delivery and maintenance of Investigator Grants exports during the bidding phase and during the template development phase of a study
  • Works closely with appropriate teams to ensure accurate, complete and timely deliveries of Investigator Grants.
  • Assists in the development and maintenance of processes, policies, SOPs and associated documents concerning Investigator Grants.
  • Liaises with the Investigator Grants team and advises Commercial Operations, Project Management, Business Development, Site Activation, Clinical Operations and Customers on forecasting strategies/risk mitigation surrounding Investigator Grants.
  • Review study protocols and liaise with competent departments as needed to complete a costing strategy for protocol-driven costs.
  • Review study budgets and costs pertaining to Investigator Grants operations and participate in Commercial Operations activities.

OTHER SKILLS AND ABILITIES:
  • Knowledge regarding global industry standard benchmarks, fair market value and proven expertise using investigator grant software (i.e. GrantPlan, Grants Manager) on a global level.
  • Experience in reviewing and understanding study protocols, study budgets, as well as other technical, medical and legal documents related to Investigator Grants.
  • Ability to work infast-paced, deadline oriented, and changing environment
  • Strong planning, strategizing, managing, monitoring, scheduling, critiquing and problem solving skills
  • Excellent written and verbal communication skills, including negotiation skills and knowledge of clinical trial agreements to clearly and concisely present information.
  • Computer expertise with document and spreadsheet applications.

REQUIREMENTS:
  • Bachelor's degree or equivalent in business administration, law, science or related field.
  • Adept knowledge of biopharmaceutical/CRO industry and applicable local regulatory requirements.
  • Knowledge and understanding of global industry standard benchmarks, fair market value, ICH and GCP Guidelines, as well as local compensation and regulatory requirements.
  • Excellent spoken and written English language skills.
  • At least 1yr experience forecasting Investigator Grants.
  • Prefer experience with investigator grant forecasting tools (i.e. GrantPlan, Grants Manager)

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Company

Find out more about working for our company

Worldwide Clinical Trials -hub-button

Brief Company Description; 

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,000 experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

 

Company info
Website
Mini-site
Worldwide Clinical Trials
Telephone
+44 115 956 7711
Location
1st Floor Waterfront House
Beeston Business Park
Beeston
Nottingham
Nottinghamshire
NG9 1LA
United Kingdom

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