Clinical Trial Assistant

4 days ago


Chennai, India ICON Full time

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives.

Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Integrity, Collaboration, Agility and Inclusion. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.

That’s our vision. We’re driven by it. And we need talented people who share it.

If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.

As a Clinical Trial Assistant at ICON, you’ll work with a collaborative and successful team to support our Clinical Trial Management and Project Management teams with operational activities. We pride ourselves on our amazing company culture, where we work as one team to achieve industry-leading results.

The role:

- Provide Support to various projects
- Maintain and Tracking clinical study documentation
- Coordinate study materials
- Collate relevant study information.

You will need:

- 1-2 years of experience in CRC
- Strong Administrative skills
- Organizational skills to support several team members.
- Excellent written and verbal communication
- Working Knowledge of computer systems including Microsoft Word, Excel, Outlook and PowerPoint
- Any Degree in Life Science

Benefits of Working in ICON:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.

We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors.

We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.

ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.



  • Chennai, Tamil Nadu, India Icon plc Full time

    ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development...


  • Chennai, Tamil Nadu, India Icon plc Full time

    ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. - With our patients at the centre of all that we do, we help to accelerate the...


  • Chennai, Tamil Nadu, India ICON Full time

    ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development...


  • Chennai, India ICON Full time

    At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Integrity, Collaboration, Agility...

  • Content Editor

    2 weeks ago


    Chennai, India Clarivate Full time

    Associate/Content Editor in the Clinical Trials team We are looking for an Associate Content Analyst/Content Analyst to join our Clinical Trails team in Hyderabad/Chennai/Bangalore. This is an amazing opportunity to work on Cortellis Clinical Trial Intelligence and Cortellis Drug Discovery Intelligence. We have a great skill set in Clinical and we would...


  • chennai, India Seven Consultancy Full time

    JOB DETAILS 1.Collaborating with Project Manager to set targets for clinical monitoring staff, and ensuring recording of trial in compliance with project goals.2.Creating and implementing study-specific clinical monitoring tools and documents.3.Creating and overseeing trial budget.4.Identifying, enlisting and choosing sites, and coordinating site...


  • chennai, India Seven Consultancy Full time

    JOB DETAILS 1.Collaborating with Project Manager to set targets for clinical monitoring staff, and ensuring recording of trial in compliance with project goals.2.Creating and implementing study-specific clinical monitoring tools and documents.3.Creating and overseeing trial budget.4.Identifying, enlisting and choosing sites, and coordinating site...

  • Clinical Research

    3 weeks ago


    Tambaram, Chennai, Tamil Nadu, India DEEPAM HOSPITAL Full time

    **Clinical Research Coordinator Job Description** Clinical research coordinators work under clinical research managers and are tasked with administering clinical trials. Their primary responsibilities include managing clinical trials and collecting data, informing participants about study objectives, and administering questionnaires. Clinical Research...


  • Chennai, India Pfizer Full time

    ROLE SUMMARYDesign, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, Pfizer standards and best practices.Provide statistical expertise and contributions for projects and protocols in support of clinical development under the supervision of senior statistical staff.Provide statistical...

  • Clinical Statistician

    2 months ago


    Chennai, India Pfizer Full time

    ROLE SUMMARY - Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, Pfizer standards and best practices. - Provide statistical expertise and contributions for projects and protocols in support of clinical development under the supervision of senior statistical staff. - Provide...

  • Clinical Statistician

    3 weeks ago


    Chennai, India Pfizer Full time

    ROLE SUMMARY Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, Pfizer standards and best practices. Provide statistical expertise and contributions for projects and protocols in support of clinical development under the supervision of senior statistical staff. Provide...

  • Clinical Statistician

    3 weeks ago


    Chennai, India Pfizer Full time

    ROLE SUMMARY Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, Pfizer standards and best practices. Provide statistical expertise and contributions for projects and protocols in support of clinical development under the supervision of senior statistical staff. Provide...

  • Clinical Statistician

    3 weeks ago


    chennai, India Pfizer Full time

    ROLE SUMMARY Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, Pfizer standards and best practices. Provide statistical expertise and contributions for projects and protocols in support of clinical development under the supervision of senior statistical staff. Provide...


  • Chennai, Tamil Nadu, India Pfizer Full time

    ROLE SUMMARY Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, Pfizer standards and best practices. Provide statistical expertise and contributions for projects and protocols in support of clinical development under the supervision of senior statistical staff. Provide...

  • Clinical Statistician

    3 weeks ago


    Chennai, India Pfizer Full time

    Role Summary: - Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, standards and best practices. - Provide statistical expertise and contributions for projects and protocols in support of clinical development under the supervision of senior statistical staff. - Provide statistical...

  • Clinical Statistician

    2 months ago


    Chennai, India Pfizer Full time

    Role Summary: - Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, Pfizer standards and best practices. - Provide statistical expertise and contributions for projects and protocols in support of clinical development under the supervision of senior statistical staff. - Provide...

  • Clinical Research

    1 week ago


    Tambaram, Chennai, Tamil Nadu, India DEEPAM HOSPITAL Full time

    Clinical Research Coordinator Job DescriptionClinical research coordinators work under clinical research managers and are tasked with administering clinical trials. Their primary responsibilities include managing clinical trials and collecting data, informing participants about study objectives, and administering questionnaires.Clinical Research Coordinator...


  • Chennai, Tamil Nadu, India Pfizer Full time

    Job Title: Data Manager at PfizerAbout the role: Joining the Data Monitoring and Management team at Pfizer means becoming a key player in ensuring the timely and high-quality review and management of clinical data for the company's portfolio.Participate in data review and query management activitiesAssist in database design and implementation of clinical...


  • Chennai, Tamil Nadu, India Seven Consultancy Full time

    JOB DETAILS 1. Ensure that clinical research studies are conducted in accordance with the protocol, standard operating procedures, good clinical practice (GCP) guidelines, and other applicable regulatory requirements.Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and GCP guidelines.Review...


  • Chennai, Tamil Nadu, India Pfizer Full time

    ROLE SUMMARY Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, Pfizer standards and best practices. Provide statistical expertise and contributions for projects and protocols in support of clinical development under the supervision of senior statistical staff. Provide statistical...