Senior Clinical Research Associate

4 weeks ago

India George Clinical Full time

We are expanding We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow.


Who are we?

  • A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence
  • 20+ years of experience, ~500 people managing 39+ geographical locations throughout the Asia-Pacific region, USA, and Europe
  • Full range of clinical trial services to biopharmaceutical, medical device, and diagnostic customers, for all trial phases, registration and post-marketing trial
  • We combine scientific leadership and global operational excellence, with strong experience in renal medicine, oncology, cardiovascular and chronic diseases across various phases to improve the health of millions worldwide.


Why work with us?

  • We are a global team making a difference in the world – our clinical trials improve the health of millions worldwide
  • Competitive salary and benefits
  • Flexible and agile working arrangements - onsite, hybrid or WFH (dependent on location)
  • Strong and diverse Learning & Development opportunities including exposure to all aspects of clinical trials with an unparalleled network of Scientific Leaders to learn from
  • A focus on employee wellbeing including global employee engagement surveys, steps challenges, reward and recognition programs, team building activities and other fun events


About the role:

The Senior Clinical Research Associate (SCRA) is a member of the Clinical Operations group in George Clinical. The Clinical Operations group is responsible for site management, monitoring tasks and support of clinical trials. The group allocates resources to projects as appropriate to assist with the implementation of project plans and to ensure compliance with regulatory requirements and Standard Operating Procedures.


Key Accountabilities:

  • Coordinate the identification, feasibility assessment and selection of investigators and sites to undertake the study
  • Prepare, plan, organise and conduct pre-study (site selection) visits and report on these visits to assist in site selection
  • Prepare and submit of regulatory and Ethics Committee packages and updates as appropriate in the local setting
  • Negotiate site budgets, co-ordinate for site contract execution & site payments, and track site payments
  • Prepare for, plan, organise and conduct site initiation visits
  • Develop and maintain appropriate monitoring tools and project specific documents
  • Motivate and train investigators and ensure that the study site personnel have a good understanding of the protocol, the investigational product and the requirements of the study and that they can fulfil their obligations to conduct the study accurately and to deadlines
  • Mentor, coach, and train junior staff members as directed by line management
  • Monitor study at allocated sites utilising both on-site and off-site activities including:
  1. Verification of quality, accuracy, completion, and timeliness of data
  2. Complete and efficient resolution of data queries, audits and issues
  3. Adherence to the study protocol, monitoring plan and other relevant project specific requirements
  4. Adherence to ICH/GCP and other regulatory guidelines and requirements as relevant to this trial including reporting of patient safety, and adverse/serious adverse events
  • Collect, review (for quality and compliance) & approve essential documents from study sites and code documents for filing
  • Reconcile contents of in-house files and site files for responsible sites
  • Complete all monitoring activities and progress reports, accurately and within the predetermined timeframe
  • Coordinate distribution, tracking, handling and destruction of Investigational Product and other study supplies per site
  • Maintain study information using the clinical trial management system and any other tracking and reporting tools for the project
  • Perform project site close-out visit and other site closure related activities
  • Any other responsibilities assigned by line manager


What are our expectations of candidates?

  • Tertiary qualifications in a related science or health care discipline
  • At least five years’ experience in clinical trial monitoring within an academic, CRO or pharmaceutical environment
  • Understanding of medical terminology and physiology
  • Ex Excellent interpersonal skills, presentation skills and the ability to work well and flexibly i.e. autonomously, in small teams and with a wide range of varying stakeholders
  • Excellent organisational skills – ability to organise, take initiative and follow up independently
  • Technological proficiency including Microsoft Office packages, electronic data capture and project management systems
  • Ability and willingness to travel (up to 50%)
  • Driving licence
  • Ability to see the big picture, yet still focus on detail and quality of work
  • Ability to be flexible and adaptable in the face of changing organisational priorities and ambiguous environments


We are searching for individuals who are excited by the idea of regional and global projects and teams, don’t want to get lost in a large CRO and are ready to have their ideas heard

You will be willing to extend yourself and take on new challenges while living our values of Mutuality, Integrity, Can-do approach, Empowerment and Excellence .


How do I apply and what if I'm interested in a role in future or want to refer someone?

Apply via LinkedIn or send your CV, referral or confidential query to and our friendly HR team across the world will reach out as appropriate soon. Please provide your full contact details, the location you are applying for, whether you are interested in a current or future opportunity and we'll be in touch. We are reviewing applications as we receive them but please note that only short-listed applicants will be contacted.


How do I learn more about the roles and George Clinical?

Follow us on Linkedin to see our regular updates and how we celebrate our people and success across our business and projects You can also visit us at

We are reviewing applications as we receive them but please note that only short-listed applicants will be contacted.



Thank you for your interest in working with George Clinical. As a global business, we are committed to handling Personal Information in accordance with applicable privacy and data protection laws in the many countries in which we do business. Please see our Privacy Policy for further information.


  • Senior Clinical Research Associate

    3 days ago

    India George Clinical Full time

    We are expanding We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow. Who are we? A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence 20+ years of...

  • Senior Clinical Research Associate

    2 weeks ago

    india George Clinical Full time

    We are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow. Who are we? A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence 20+ years of...

  • Senior Clinical Research Associate

    4 weeks ago

    india George Clinical Full time

    We are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow. Who are we? A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence 20+ years of...

  • Guard Clinical Research Associate

    4 weeks ago

    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...

  • Business Development Manager-Clinical Services and Pharma

    4 weeks ago

    india MS CLINICAL RESEARCH Full time

    Job Title : Business Development Manager-Clinical Services and Pharma Location : Bengaluru Company : MS Clinical Research Pvt Ltd About Us: MS Clinical Research Pvt Ltd is a leading organization in the clinical research industry, providing comprehensive clinical services to the pharmaceutical sector. We are committed to advancing scientific knowledge and...

  • Business Development Manager-Clinical Services and Pharma

    3 days ago

    India MS CLINICAL RESEARCH Full time

    Job Title : Business Development Manager-Clinical Services and Pharma Location : Bengaluru Company : MS Clinical Research Pvt Ltd About Us: MS Clinical Research Pvt Ltd is a leading organization in the clinical research industry, providing comprehensive clinical services to the pharmaceutical sector. We are committed to advancing scientific knowledge and...

  • Clinical Research Associate

    2 weeks ago

    India ICON plc Full time

    As a (Clinical Research Associate) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. **Clinical Research Associate** **India - Delhi and Bangalore** - **What you will be doing**: - Site Monitoring - SIV ~ COV - PI Management - audit & inspection **You are**: - more than 2...

  • Clinical Research Associate

    3 days ago

    India ICON plc Full time

    As a (Clinical Research Associate) you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence.Clinical Research AssociateIndia - Delhi and Bangalore- What you will be doing:Site Monitoring SIV ~ COV PI Management- audit & inspectionYou are:- more than 2 years of site monitoring experience-...

  • Clinical Research Coordinator

    2 months ago

    india Learning Labb Research Institute Full time

    We are seeking a motivated and detail-oriented Clinical Research Coordinator to join our dynamic team. As a Clinical Research Coordinator, you will play a crucial role in the planning, implementation, and coordination of clinical research studies. You will work closely with principal investigators, study participants, and other healthcare professionals to...

  • Clinical Research Associate

    1 week ago

    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...

  • Inhouse Clinical Research Associate

    1 week ago

    India Novotech Full time

    **Brief Position Description**: The Inhouse Clinical Research Associate (IHCRA) provides in-house support to the clinical team according to project requirements, ICH GCP guidelines, local or global regulatory requirements and Novotech or Client SOPs **Minimum Qualifications & Experience**: - Relevant experience/qualifications in Life Sciences or related...

  • Inhouse Clinical Research Associate

    3 days ago

    India Novotech Full time

    Brief Position Description:The Inhouse Clinical Research Associate (IHCRA) provides in-house support to the clinical team according to project requirements, ICH GCP guidelines, local or global regulatory requirements and Novotech or Client SOPsMinimum Qualifications & Experience: Relevant experience/qualifications in Life Sciences or related field or...

  • Clinical Data Manager

    1 month ago

    india George Clinical Full time

    We are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow. Who are we? A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence 20+ years of...

  • Clinical Data Manager

    1 month ago

    india George Clinical Full time

    We are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow. Who are we? A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence 20+ years of...

  • Clinical Research Associate in US

    4 weeks ago

    india Cetas Healthcare Full time

    Job Description What you'll be doing:You shall be required to share your expert opinion in the following areas for which you shall be paid a consulting fee:You shall need to share your medical expertise in medical procedures, workflows, problems faced in performing patient care or in day-to-day activity, etc. Your expertise and opinions shall be valuable to...

  • Clinical Research Associate in US

    3 days ago

    India Cetas Healthcare Full time

    Job Description What you'll be doing:You shall be required to share your expert opinion in the following areas for which you shall be paid a consulting fee:You shall need to share your medical expertise in medical procedures, workflows, problems faced in performing patient care or in day-to-day activity, etc. Your expertise and opinions shall be valuable to...

  • Research Associate

    3 days ago

    India Nutrihub ICAR-IIMR Full time

    Name of the post : Research Associate (1 Post) Project : NFSM (In – Vivo Health Benefits) Emoluments : Rs. 49,000/- per month + HRA for master degree holders & Rs. 54,000/- per month + HRA for Ph.D holders (HRA as per ICAR rules) Project till : April, 2025 Essential Qualifications: With Doctoral Degree: Ph.D. in Food Sciences & Nutrition/ Food...

  • Research Associate

    4 weeks ago

    india Nutrihub ICAR-IIMR Full time

    Name of the post : Research Associate (1 Post) Project : NFSM (In – Vivo Health Benefits) Emoluments : Rs. 49,000/- per month + HRA for master degree holders & Rs. 54,000/- per month + HRA for Ph.D holders (HRA as per ICAR rules) Project till : April, 2025 Essential Qualifications: With Doctoral Degree: Ph.D. in Food Sciences &...

  • Senior Associate- Clinical Negligence

    2 months ago

    india Themis Recruit Full time

    Job Description Our client, a leading national law firm specialising in Clinical Negligence, are seek an adept Clinical Negligence Solicitor to join their team as a Senior Associate, with prospects for advancement to Head of Department. In this role, you'll oversee a varied caseload of high-value medical negligence claims, contribute to business development,...

  • Clinical Research Associate

    1 week ago

    India ICON plc Full time

    As a (job title) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. **What you will be doing**: - The CRA role is now a field monitoring specialist (standardization & harmonization across countries) - The CRA is expected to be a site relationship manager and the main point of...