Site Intelligence Lead

  • location: Groton, CT
  • type: Contract
  • salary: $34.46 - $40.54 per hour
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job description

Site Intelligence Lead

job summary:
As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. With therapeutic areas that include Oncology, Vaccines, and Rare Diseases, our partner aims to make treatments streamlined, easily accessible, and globally produced. If you share their goal of approaching healthcare in a novel way, look no further - apply for your dream job now!

location: Groton, Connecticut
job type: Contract
salary: $34.46 - 40.54 per hour
work hours: 9 to 5
education: Bachelors
- Partners with Clinical Operations to develop and deliver Site Intelligence plans.

- Performs tasks for multiple Site Intelligence projects.

- Supports Study Optimization Leadership/Head of Site Intelligence on special projects

- Leads and/or participates in global initiatives to improve operational efficiencies.

- Works under close supervision of Head of Site Intelligence & Site Selection

- Supports, manages processes relating to Country & Site Intelligence.

- Maintains continuity connecting and documenting work performed by the Feasibility Lead in Early Estimates, Early Feasibility, Detailed Assumptions, Detailed Feasibility, to Site Selection.

- Supports the build of the investigator database, collection of information supporting the definition of the ideal site for a study, identification of suitable sites for a study, and coordinates global efforts for site intelligence.

- Acts as primary contact for the study team in the site intelligence process. Participates in the site intelligence by leading the preparation of the country plan for the study (number of sites proposed, type of sites, recruitment rates, and key challenges) coordinating site intelligence resources to ensure timely completion of tasks and high quality.

- Engages with therapeutic business units to support and deliver the implementation and delivery of specific site intelligence initiatives through good communication, clear implementation plans and explicit performance metrics to agreed timelines and quality,

- Creates awareness by working as a cross functional team leader to deliver site intelligence initiatives with a variety of stakeholders, both internal and external. Initiatives will be diverse and may include technology and process improvement components.

- Supports and maintains to the development of relevant information libraries and communication materials to assist with site intelligence activities.

- Additionally runs operational and technical aspects of large global projects and assists with other Company systems activities related to the site intelligence.

- Promotes a continuous improvement culture to streamline appropriate processes for maximum efficiency and productivity

Experience in a clinical research organization and related therapeutic specialties with familiarity in principles, concepts, practices and standards. History of success in a customer service role with demonstration of meeting customer expectations.


- Reports to Head of Site Intelligence & Site Selection

- Manages relationships with RU and BU Clinical Development Group Heads and CRO Partners.

- Partners with CD&O, RU/BU facing teams, and protocol assigned roles

- Partners with Business Process Owners

- Supports GPD RU/BU Heads and CD&O LT

- Partners with Finance, GPD, CD&O Business Operations and Procurement Groups

Education & Qualifications

  • Bachelor of Science/Equivalent + 8 years work experience
  • Master of Science + 6 years work experience
  • PhD/MD + 4 years work experience
  • Mandatory to have prior Feasibility experience.
  • Nice to have: CRO experience
  • Ability to multitask under tight deadlines on several projects with specific and unique requirements, while providing attention to detail and high quality work 4 - 6 Years
  • Demonstrated knowledge of clinical research processes and regulatory requirements 2 - 4 Years
  • Demonstrated success/results in prior roles including matrix organization 2 - 4 Years
  • Excellent verbal, written, communication and time management skills 4 - 6 Years
  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, database applications) 4 - 6 Years
  • Project management skills 2 - 4 Years
  • Strong data analytical skills 4 - 6 Years
  • Strong presentation skills, interpersonal skills, as well as a team oriented approach. 2 - 4 Years
skills: Project Management, Clinical research, MS-WORD, MS-EXCEL, MS-Powerpoint, MS-Project
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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