Clinical Research Associate

6 days ago

Chennai, India Icon plc 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: Accountability & Delivery, Collaboration, Partnership and Integrity. 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 Research Associate at ICON, you’ll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II - IV, ensuring adherence to applicable regulations and principles of ICH-GCP.

The role:

- Independent, proactive work to set up and monitor studies, complete reports and maintain documentation
- Submitting protocol, consent documents for ethics/IRB approval, as well as preparing regulatory submissions
- Balancing sponsor generated queries
- Taking responsibility for study cost efficiency
- Preparation and review of study documentation and feasibility studies for new proposals
- Potential to assist in training and mentoring fellow CRAs

You will need:

- 24 months+ of monitoring experience in phase I-III trials as a CRA
- College degree in medicine, science, or equivalent
- Previous monitoring experience in medium-sized studies, including study start-up and close-out
- Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data
- Excellent written and verbal communication in English and local language
- Ability to work to tight deadlines

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 fulfill 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.

Are you a current ICON Employee? Please click here to apply:
link

  • Clinical Research Coordinator

    18 hours ago

    Chennai, India SYS Research Full time

    **Job description** **Responsibilities for Clinical Research Coordinator** - Responsible for ensuring study is compliance with local and federal laws and regulations - Recruits and screens potential study participants and performs intake assessments - Creates and/or maintains all documents and records related to the study - Acts as a point of reference for...

  • Senior Clinical Research Coordinator

    6 days ago

    Chennai, Tamil Nadu, India Apollo Research and Innovations Full time ₹ 9,00,000 - ₹ 12,00,000 per year

    Role DescriptionThis is a full-time on-site role for a Senior Clinical Research Coordinator, located in Chennai. The Clinical Research Coordinator will be responsible for managing clinical trials, ensuring informed consent is obtained, and adhering to research protocols. The role involves coordinating and overseeing day-to-day research activities,...

  • Senior Clinical Research Associate

    3 hours ago

    Chennai, Tamil Nadu, India Sapien Biosciences Full time ₹ 9,00,000 - ₹ 12,00,000 per year

    See Sapien LinkedIn for multiple job openings at multiple locations:Location: Hyderabad, Mumbai, Kolkata, ChennaiQualification: M.Sc in Life Sciences, Biotechnology, Molecular Biology, or related fieldExperience: Minimum 2.0 years relevant work experience in biobanking, DatabaseManagement / Clinical Research Organization (CRO).About the RoleSapien...

  • Jobs For Clinical Research Associate

    2 weeks ago

    Chennai, 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.2. Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and GCP guidelines. 3....

  • Jobs For Clinical Research Associate- Medical

    2 weeks ago

    Chennai, 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.2. Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and GCP guidelines. 3....

  • Clinical Coordinator

    1 week ago

    Chennai, India Chettinad Hospital & Research Institute Full time

    Should Complete Msc. Neuro Science - Knowledge of medical and clinical research terminology and processes. - Ability to follow and provide critical feedback on the investigational plan. - Ability to develop study related budgets, contracts, and patient consent documents. - Regulations associated with the conduct of clinical trials and other related research...

  • Research Associate

    19 hours ago

    Chennai, Tamil Nadu, India DataSolve Analytics Private Limited Full time

    **Role**: Research Associate (Web Research) **Degree**: BSc. / MSc. **Discipline**: Biochemistry, Biotechnology, Microbiology To research various web sources and databases to capture data based on the project requirements, which include web research, reviewing scientific literature, industry associations, clinical trials, clinical practice guidelines,...

  • Clinical Research Associate

    1 week ago

    Chennai, Tamil Nadu, India sun pharmaceutical ltd. Full time ₹ 5,00,000 - ₹ 12,00,000 per year

    Job Description Job Location: ChennaiYOUR TASKS AND RESPONSIBILITIES:Perform site feasibility, identify potential investigator, negotiate study budget with potential investigators, finalization of investigators, sites, and execution of CDA and study-related contracts Preparation and submission of study documents for EC permission for respective study...

  • Product Manager

    3 weeks ago

    Chennai, India Tilda Research Full time

    Product Manager (AI for Clinical Research)About the RoleWe're looking for a Product Manager who combines strong analytical and technical foundations with deep fluency in AI tools and applications. You'll work directly with the founders to shape our product strategy, prioritize features that deliver immediate customer value, and ensure we're building AI...

  • Clinical Research Associate

    4 days ago

    Chennai, Tamil Nadu, India ICON Full time

    **Home-based, Location: Chennai** As a **Clinical Research Associat**e you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You will have an opportunity to work in a solid partnership and an environment driven by innovation and continuous improvement. This program is for you if...