Roche

Clinical Trial Coordinator

Roche

Indianapolis, IN, USA
Full-TimeDepends on ExperienceSenior LevelMasters
Job Description

We are seeking an experienced and motivated Clinical Trial Coordinator to join the Roche team. The ideal candidate will have a strong combination of organization, project management, and interpersonal skills. This position requires a highly-organized and detail-oriented professional with a passion for clinical research.The Clinical Trial Coordinator will support various clinical trial activities, from study start-up to close-out. This role requires a team-oriented individual with excellent communication and problem solving skills who can work independently. The Clinical Trial Coordinator will coordinate activities across both internal and external stakeholders, as well as ensure projects are adhering to regulatory requirements. To be successful in this position, the ideal candidate is required to have a Bachelor’s Degree in a relevant field, such as life sciences, nursing, or public health. Previous experience in clinical research and project management will be considered a plus. The Clinical Trial Coordinator must have a proven record of success in multitasking, excellent written and verbal communication, and customer service.

Responsibilities: • Plan and coordinate various clinical trial activities, from study start-up to close-out • Monitor progress of clinical trial activities and ensure compliance with regulatory requirements • Facilitate communication between internal and external stakeholders • Track progress of clinical trials and report to management • Assist with the development of study protocols and associated documents • Prepare and review documents for regulatory submission • Manage budgets, timelines, and resources for clinical trials • Monitor compliance with Good Clinical Practice (GCP) guidelines • Provide guidance and support to clinical trial staff • Maintain accurate and up-to-date documentation of clinical trial activities • Train new clinical trial personnel on study protocols and procedures

Where is this job?
This job is located at Indianapolis, IN, USA
Job Qualifications
  • Bachelor's Degree In A Related Field

  • Project Management

  • Excellent Organizational And Communication Skills

  • Knowledge Of Medical Terminology And Clinical Trial Regulations

  • Experience In Data Management

  • And The Ability To Multi-Task

  • Strong Computer Skills

  • Including Proficiency In Microsoft Office

  • Experience In The Pharmaceutical

  • Medical Device

  • Or Biotechnology Industry

  • Ability To Work Independently And Collaboratively With A Team

  • Ability To Adhere To Strict Deadlines

Required Skills
  • Project Management

  • Data Entry

  • Data Analysis

  • Clinical Research

  • Database Management

  • Auditing

  • Reporting

  • DOCUMENT CONTROL

  • Clinical monitoring

  • Site management

  • Compliance monitoring

  • Regulatory Affairs

  • Clinical Trials

  • Protocol Development

  • Clinical Data

Soft Skills
  • Communication

  • Leadership

  • Time management

  • Interpersonal Skills

  • creativity

  • self-motivation

  • flexibility

  • Teamwork

  • Adaptability

  • Problem-Solving

Compensation

According to JobzMall, the average salary range for a Clinical Trial Coordinator in Indianapolis, IN, USA is $38,922 to $68,786. The median salary for this role is $54,875.

Additional Information
Roche is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
Required LanguagesEnglish
Job PostedOctober 6th, 2023
Apply BeforeJuly 20th, 2025
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About Roche

Roche Holding AG operates as a research healthcare company. It operates through the diagnostics and pharmaceuticals segments. The pharmaceutical segment refers to development of medicines in the field of oncology, immunology, ophthalmology, infectious diseases and neuroscience. The diagnostic segment refers to diagnosis of diseases through an in vitro diagnostics process.

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