Clinical Research JDs

Clinical Research Division
at Patanjali Research Foundation, Haridwar, INDIA
Patanjali Research Foundation is a fully integrated innovative research institute to conduct

modern experimentation on Ayurvedic medicines for the treatment of various diseases. The
Institute has a diversified research portfolio and a substantial clinical testing pipeline. With its
R&D centre and headquarter in Haridwar, Patanjali also has a mega manufacturing facility, an
Ayurvedic hospital and medical college, a University, and herbarium along with herbal garden.
Research laboratories at Patanjali are accredited with NABL, DSIR, DBT, and have CPCSEA
approved animal house along with well-defined IAEC, IBSC and IEC structures. These are
probably one-of-the-kind, and literally state-of-the-art facilities to conduct research on
Ayurveda. Top of the line equipments and globally trained workforce energizes the research
operations, on a daily basis.
The Clinical Research Division is looking for suitable candidates for these 2 positions. Please see
details below.
(1) Clinical Trial Coordinator/Site Monitor (Job code: 23/CR/02)

(2) Clinical Biostatistician (Job code: 23/CR/03)
D4, PRF 2023 Page 1

(1) Clinical Trial Coordinator/Site Monitor
(Job code: 23/CR/02)
The Clinical Trial Coordinator plays a critical role in supporting the planning, implementation,
and management of clinical trials. They work closely with various stakeholders, including
principal investigators, study teams, regulatory bodies, and sponsors, to ensure the smooth
execution of clinical research studies.
Key Responsibilities:
 Study Planning and Documentation: Assist in the development of study protocols, CRF,
ICR, and other study-related documentation.
 Study Coordination: Coordinate and schedule study-related activities, including
participant recruitment, screening, enrollment, and follow-up visits. Liaise with study
sites, investigators, and research staff to provide guidance and support for study
implementation.
 Data Collection and Management: Oversee data collection activities, including the
development and implementation of data collection tools and systems. Ensure accurate
and timely entry of study data into the electronic data capture (EDC) system or other
designated databases. Perform data quality checks and resolve data discrepancies in
collaboration with the data management team.
 Study Monitoring and Reporting: Assist in monitoring the progress of clinical trials,
ensuring adherence to timelines and study milestones. Contribute to the preparation of
study reports, presentations, and publications.
Qualifications and Skills:

 Minimum qualification is Bachelor's degree in life sciences, nursing, pharmacy, or a
related discipline. Master's or Ph. D qualification is preferred for certain positions.
 Prior experience in clinical research as clinical trial coordination is highly desirable.
 Must have knowledge of Good Clinical Practice (GCP) guidelines, applicable regulatory
requirements (e.g., Indian, FDA, EMA), and ethical considerations in human subjects
research.
 Familiarity with electronic data capture (EDC) systems and other clinical trial
management tools.
 Proficiency in using common software applications (e.g., Microsoft Office suite, data
analysis tools).
 Flexibility and adaptability to navigate changing priorities and evolving study
requirements.
D4, PRF 2023 Page 2

(2) Clinical Biostatistician
(Job code: 23/CR/03)
The Clinical Biostatistician plays a crucial role in the design, analysis, and interpretation of
clinical research studies. With 2-4 years of experience in the field, the Clinical Biostatistician
contributes to the statistical planning and execution of clinical trials, collaborates with cross-
functional teams, and supports the generation of high-quality data for evidence-based
decision-making. They are responsible for statistical analysis, data management, and ensuring
compliance with regulatory guidelines and industry standards.
Key Responsibilities:
Study Design and Planning:
 Collaborate with study teams and researchers to develop study protocols, including
sample size calculations, randomization procedures, and statistical analysis plans (SAPs).
 Provide statistical input on study endpoints, study design, and statistical methodologies.
 Assist in the development of data collection tools, including case report forms (CRFs)
and electronic data capture (EDC) systems.
Statistical Analysis and Data Management:

 Perform statistical analysis of clinical trial data using appropriate statistical techniques.
 Validate and interpret statistical results, ensuring accuracy and consistency.
 Conduct exploratory data analysis (EDA) and generate tables, figures, and listings (TFLs)
to support study reporting.
 Collaborate with data management teams to ensure high-quality and complete data
collection.
Regulatory Compliance and Reporting:

 Ensure compliance with regulatory requirements, including submission of statistical
analysis plans (SAPs) and other study-related documents.
 Assist in responding to regulatory queries and requests related to statistical analyses
and study results.
Qualifications and Skills:

 Master's degree Statistics and Data Science.
 2-4 years of experience as a biostatistician in a clinical research setting (CRO, Hospital
and Pharmaceutical industry).
 Experience in analyzing and reporting clinical trial data, including familiarity with TFL
generation.
 Excellent problem-solving and critical thinking skills.
 Ability to work independently and manage multiple priorities effectively.
 Knowledge of clinical trial data management processes and systems is a plus.
D4, PRF 2023 Page 3
Patanjali Research Foundation is an equal opportunity employer and does not discriminate
against any applicant because of race, colour, religion, gender, national origin, age and physical
disability.
How to Apply
 Visit https://patanjali.res.in/career.php OR
 Write to [email protected] with your detailed CV and career aspirations.
 Mention Clinical Trial Coordinator/Site Monitor OR Clinical Biostatistician, citing
respective Job Code.
 List three professional references other than your friends and family.
D4, PRF 2023 Page 4

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Clinical Research Division

at Patanjali Research Foundation, Haridwar, INDIA

Patanjali Research Foundation is a fully integrated innovative research institute to conduct

(1) Clinical Trial Coordinator/Site Monitor (Job code: 23/CR/02)

D4, PRF 2023 Page 1

Qualifications and Skills:

D4, PRF 2023 Page 2

Statistical Analysis and Data Management:

Regulatory Compliance and Reporting:

Qualifications and Skills:

D4, PRF 2023 Page 4

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