Clinical Research Associate (CRA)

Job Description

JOB TITLE

Clinical Research Associate (CRA)

REPORTING TO

Nikita Bathla

LOCATION

New Delhi

OPEN ENDED /

FIXED TERM (Duration)

Two-year appointment extendable based on performance and institutional opportunities.

FULLTIME EQUIVALENT

3.0

JOB FAMILY

Projects

CAREER STEP

Intermediate

About The Goerge Institute

We are a medical research institute affiliated with leading universities aiming to challenge the status quo in health care. With 700 people around the world and projects in over 40 countries our Strategy 2025 is all about impact specifically the impact of The George Institutes activities on the health of millions of people particularly those living in disadvantaged circumstances around the world.

Our strategy focuses on three key research priorities:

Better Treatments: finding better treatments for the worlds biggest health problems

Better Care: transforming primary health care to support better health for more people

Healthier Societies: harnessing the power of communities governments and markets to improve health

Our innovative commercial enterprises help maximise our impact.

Here is a sample of the things we are doing to achieve our goal of having the greatest possible impact on global health:

We are identifying better and safer treatments for the biggest killers like stroke heart disease and high blood pressure;

In many countries our award winning FoodSwitch smartphone app is helping people make healthy food choices when shopping;

In China we ran a successful education and awareness program to reduce the amount of salt eaten by people by 25% each day

In rural India we have shown that mobile technology can help diagnose mental health as well as help treat cardiovascular disease and were looking at similar approaches to treating chronic diseases in Indonesia and China;

Together with Aboriginal communities in NSW Australia we developed an innovative community led program to assist young Aboriginal drivers attain their license now implemented in a dozen of locations;

We are developing an affordable dialysis machine with potential to save millions of lives each year and transform the way kidney disease is treated globally.

George Institute Services India

George Institute Services India Pvt Ltd (GIS) is a step-down subsidiary of The George Institute for Global Health Australia (TGI) and has been set up as a commercial for-profit entity to provide advisory and consulting services in the healthcare space undertake commissioned research and provide various services to overseas group entities.

Context of the Role

Non-communicable diseases (NCDs) cause over 70% of all deaths worldwide each year. 85% of premature deaths due to NCDs are in low- and middle-income countries. The George Institute is focused on finding better treatments for the worlds biggest health problems including renal and cardiovascular diseases.

We are conducting large-scale clinical trials often across multiple countries and clinical sites and developing new medicine and technology solutions to prevent and treat common chronic and critical conditions with a global perspective.

Our work is transforming practice and improving health outcomes worldwide. A Clinical Research Associate (CRA) will work on trials testing new and existing drugs and will typically be involved in all stages of the clinical trial including identifying an investigational site and setting up initiating monitoring and closing down the trial.

Reporting Relationships

Directly reports to Senior Project Manager

Duties and Key Responsibilities

The Clinical Research Associate would be expected to:

• Assist in the development of trial related documents including but not limited to the protocol investigators brochure patient information documents and care report forms
• coordinate with the ethics committee which safeguards the rights safety and wellbeing of all trial subjects
• assist in regulatory authority applications and approvals that oversee the research and marketing of new and existing drugs
• assess the suitability of facilities to use as the clinical trial site
• assist in the selection of an investigator who will be responsible for conducting the trial at the trial site
• liaise with doctors consultants or investigators on conducting the trial
• set up the trial sites - ensuring each centre has the trial materials including the trial drug often known as the investigational medicinal product (IMP)
• train the site staff to trial-specific standards
• monitor the trial throughout its duration which involves visiting the trial sites on a regular basis and dealing with and solving any issues
• verify that data entered on to the CRFs is consistent with patient clinical notes known as source data/document verification (SDV)
• collect completed CRFs from hospitals and general practices
• write visit reports and file and collate trial documentation and reports
• meet with team members to discuss on-going trials results and any trends or adverse events
• ensure all unused trial supplies are accounted for
• close down trial sites on completion of the trial
• archive study documentation and correspondence
• prepare final reports for sponsors regulatory authorities and ethics committees

As a Team Member:

• Participate in team meetings and activities relating to the Leprosy trial and own work area;
• Participate in special projects to improve processes tools systems and organisation;
• Take responsibility for personal learning and development and for setting achievable and meaningful work objectives and managing personal targets meeting obligations of the Institutes Performance Management and Development Policy;
• Demonstrate commitment to GIs values including performing to an exceptionally high ethical standard and focus on integrity collaboration and teamwork in all efforts.

Work Health and Safety

• Comply with Work Health and Safety legislation and operate in accordance with established Occupational Health and Safety practice and procedures at the Institute.
• Promote and contribute to a safe secure environment for staff and visitors.

Skills Knowledge and Experience

• Qualifications: Qualification in life sciences medical sciences or nursing with;
• Experience of at least 2 years in clinical trial coordination;
• Willingness to travel to conduct frequent site monitoring visits;
• Demonstrated capability to produce outcomes and achieve objectives within agreed time periods;
• Strong problem solving analytical skills and proven strategic thinking;
• Demonstrated resourcefulness with ability to influence others to achieve common goals;
• Excellent interpersonal skills with high level of proficiency in English and the ability to work well autonomously;
• Excellent team-work skills with demonstrated ability to collaborate in small teams and with a wide range of varying stakeholders;
• Ability to demonstrate flexibility and to be adaptable to changing organisational priorities and ambiguous environments;
• Strong focus on producing the highest quality of work and on ensuring optimum accuracy of outputs;
• Well organised and efficient with the capacity to work under pressure.

For more details please see the Position Descriptionfor this role.

How to apply:

Interested candidates should send their resume with full contact details current and expected CTC/salary and notice period details. Clearly mentioning the job title <Clinical Research Associate (CRA)> in the subject line to by 28 September 2025.

Our big and bold mission to improve the health of millions of people worldwide needs a diverse and innovative team to deliver it. So we foster a dynamic inclusive and flexible workplace where each individual can bring their best selves to work.

Everyone is encouraged to apply including people from culturally and linguistically diverse backgrounds people with a disability people of all gender identities and sexual orientations and mature-aged adults.