Site Identification Analyst II

Posted 2 Days Ago
Be an Early Applicant
Hiring Remotely in United States of America
Remote
Mid level
Biotech • Pharmaceutical
The Role
Supports clinical trial site identification and start-up activities by managing site outreach, tracking CTMS milestones, maintaining investigator data, coordinating site questionnaires, preparing progress reports, and monitoring project requirements. The role collaborates with internal teams, sponsors, vendors, and investigators while supporting reporting systems, metrics, and data quality. Candidates need clinical operations or data management experience in pharmaceutical, biotech, or medical device environments, plus CTMS and EDC knowledge.
Summary Generated by Built In
Premier Research is looking for a Site Identification Analyst II to join our Clinical Monitoring, Site Management and SSU team.

You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success.

  • We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires.

  • Your ideas influence the way we work, and your voice matters here.

  • As an essential part of our team, you help us deliver the medical innovation that patients are desperate for.

Join us and build your future here.

What You'll Be Doing:  

  • Proactively builds and maintains internal and external relationships to support the gathering of business intelligence to support financial & specific operational activities 
  • Oversees site outreach for post award Site ID activities
  • Progresses and tracks in the CTMS site identification activities according to study timelines; manages time and project requirements based on study contract and works with internal and external customers/vendors to meet project specific goals.  
  • Provides weekly project progress reports to Internal and External project teams including department management; may provide information from the Investigator Database regarding timelines, site contact information, PI specialty, etc. Updates Investigator Database with new sites and investigators, reviewing entries for duplicates, and any information obtained during the site selection process as well as after studies have completed. 
  • Oversees the distribution, tracking and review of SRQs for completeness, site capability and availability based on project specific requirements and needs; identifies, monitors, documents, and tracks out-of-scope activities. 
  • Assists in the design and implementation of all relevant systems including, but not limited to, the site identification metrics and reporting, surveys, etc.

Please note the official title for this position is: Clinical Business Operations Analyst II - Systems and Data

 

What We Are Searching For:

  • Undergraduate degree or its international equivalent preferably in the Sciences or in a related field from an accredited institution 
  • Three years of data management, clinical operations, or start-up experience in the Pharmaceutical, Biotech, and Medical Device industry 
  • Two years' experience in supporting CTMS 
  • ​Experience in clinical trials support, site partnership management, site identification/selection or pharmaceutical industry highly prioritized
  • Strong analytical and problem-solving skills   
  • Good working knowledge of Clinical database applications such as EDC and CTMS  

Premier Research is proud to be an equal opportunity employer that is compliant with all federal guidelines. All qualified applicants will receive equitable consideration without regard to race, color, religion, sexual orientation, gender identity, national origin, disability or veteran status

Skills Required

  • Undergraduate degree or international equivalent, preferably in science or a related field, from an accredited institution
  • Three years of data management, clinical operations, or study start-up experience in the pharmaceutical, biotech, or medical device industry
  • Two years of experience supporting Clinical Trial Management Systems
  • Experience in clinical trial support, site partnership management, site identification or selection, or the pharmaceutical industry
  • Strong analytical and problem-solving skills
  • Working knowledge of clinical database applications such as EDC and CTMS
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The Company
HQ: Morrisville, NC
2,279 Employees
Year Founded: 1989

What We Do

We’re out to change the course of medical science. Are you ready to rise to the challenge? Premier Research is not about being everything to everyone. Instead, our deep, focused expertise targets the therapeutic areas and indications where today’s biotech and specialty pharma pioneers are doing the most amazing work. We’re 1,500 employees strong and operate in more than 20 countries, delivering unmatched expertise, operational skills, and dedication to meeting customers’ most challenging needs. Join us and meet some of the brightest minds in clinical development today — people who apply their best thinking to every project, recognizing that what they do significantly affects the lives and well-being of customers, patients, physicians, and colleagues. You’ll enjoy great benefits and very flexible working conditions in a company that values your contributions, rewards your achievements, and is committed to helping you reach your full potential. Are you ready to make a real difference and help us transform this exciting industry? Follow our company page for more information about us and the work we do, and check out our current openings for your next career move!

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