703 Clinical Manager jobs in India
Registered Nurse Level 2 - Clinical Manager
Posted today
Job Viewed
Job Description
Registered Nurse Level 2 - Clinical Manager (
Job Number:
02NS3)
Description
Employment Type: Full Time, Permanent
Classification: Registered Nurse Level 2 (P26407)
Salary: $110,733 – $117,053 (Plus 12% Super)
Location: Canberra Health Services
Section: Mental Health, Justice Health, and Alcohol & Drugs Services
Closing Date: 28th August 2025
What can we offer you:
•
City living without the traffic – click here to see why you should live in Canberra.
•
Competitive pay rates and excellent working conditions within a tertiary hospital.
•
Salary Packaging with many options that provide full fringe benefits tax concessions.
•
Flexible working conditions.
•
Reimbursement of relocation expenses for interstate candidates (subject to review and approval).
To find out more on what a career at CHS can give you, the benefits of working with us and why Canberra is Australia's happiest city click here: Benefits of working with us - Canberra Health Services (act.gov.au)
About the Role:
Join the passionate team at Mental Health, Justice Health and Alcohol and Drug Services (MHJHADS), where you'll help deliver life-changing care across inpatient, outpatient, and community settings—including people’s homes. Based in Community Recovery Services, you'll work with a multidisciplinary team to support adults experiencing complex mental health challenges. With strong clinical governance, psychiatrist collaboration, and a recovery-focused model, you’ll provide face-to-face care that empowers clients to thrive. This role offers opportunities to lead, mentor, and contribute to quality initiatives, including Clozapine Clinic delivery, while partnering with families and service providers to achieve the best outcomes.
For more information regarding the position duties click here for the Position Description.
Please note prior to commencement successful candidates will be required to:
•
Undergo a pre-employment National Police Check.
•
Comply with Canberra Health Services Occupational Assessment, Screening and Vaccination policy.
To Apply:
Please apply online by submitting a copy of your CV along with a 2-page cover letter or pitch, responding to the Selection Criteria, listed in the Position Description.
***Please note applications submitted via an agency will not be accepted for this position***
Canberra Health Services (CHS) is focussed on the delivery of high quality, effective, person centred care. It provides acute, sub-acute, primary and community‐based health services, to the Australian Capital Territory (ACT) and surrounding region. More information can be found on the CHS website.
Our Vision : creating exceptional health care together
Our Role : to be a health service that is trusted by our community
Our Values : Reliable, Progressive, Respectful and Kind
CHS is committed to workforce diversity and to creating an inclusive workplace. As part of this commitment, we welcome applications from all diversity groups. Aboriginal and Torres Strait Islander peoples, people with disability and people who identify as LGBTQIA+ are particularly encouraged to apply.
The new state-of-the-art Building 5 is now officially open at Canberra Hospital. This 44,000sqm, nine-storey facility, the largest healthcare infrastructure project in the Territory’s history, delivers cutting-edge acute clinical services. Building 5 seamlessly integrates with existing campus buildings, ensuring smooth public access, patient transportation, and efficient logistics.
If you would like further information regarding this opportunity, please contact Vanessa Reid at
#LI-DNI
Job
: Registered Nurses & Midwives
Salary Range
: 110,733.00 - 117,053.00
Closing Date
: 29/Aug/2025, 1:59:00 PM
Clinical Data Manager
Posted 2 days ago
Job Viewed
Job Description
Role : Associate Manager - Clinical Data Management
Location : Chennai, Tamil Nadu
Experience : 10+ Years
Requirements:
- 10-12 years of experience in clinical trial/data management and data operations.
- Minimum 4-5 years of people management (preferred) experience with proven supervisory
- skills.
- Extensive experience with CTMS platforms (CRIO, RT CTMS, Veeva Vault CTMS, or similar).
- Strong background in EDC systems management and clinical data operations.
- Experience in pharmaceutical, biotechnology, or CRO environment across multiple
- therapeutic areas.
Technical Expertise
- CTMS configuration and administration skills (Having knowledge in CRIO is an advantage).
- Deep knowledge of EDC platforms and system integrations.
- Strong understanding of regulatory requirements (HIPPA, FDA, EMA, ICH-GCP).
- Experience with electronic systems validation and 21 CFR Part 11 compliance.
Clinical Data Manager
Posted 4 days ago
Job Viewed
Job Description
Experience: 5+ yrs
Work Mode: Work from Office
Work Location: Bangalore
LOOKING FOR IMMEDIATE JOINERS ONLY
Job Description - Clinical Data Manager :
OVERVIEW
The Clinical Data Manager (CDM) is an independent role responsible for supporting the study team and developing comprehensive study documentation, designing database specifications, and overseeing validation, maintenance/data cleaning, and closeout activities for clinical trial databases. The CDM is recognized as the platform expert, leveraging cutting-edge tools and technologies to provide continuous data insights and ensure the timely delivery of high-quality results for Sponsors. The CDM has a strong foundation in clinical data management, combined with the agility to adapt as processes evolve towards the integration of clinical data science.
KEY TASKS & RESPONSIBILITIES
• Define project specifications for Data Management services, including Protocol Conversion, Database Build, CRF Design and Data Review and Data Reconciliation tools.
• Understand external data collection, its integration into the clinical trial, and the management and reconciliation processes required to ensure its accuracy and relevance.
• Execute data cleaning strategies to accelerate the time to achieve subject data cleanliness and ensure high-quality, timely deliverables.
• Perform holistic data review and trending analysis via reporting and elluminate® analytics to proactively identify issue, risks and develop mitigation strategies.
• Utilize artificial intelligence (AI) and machine learning (ML) for anomaly and outlier detection to enhance the efficiency and quality of trial data.
• Monitor and interpret key performance indicators (KPIs), metrics, dashboards, Clinical Trial Operational Analytics (CTOA), and reports to provide actionable recommendations to study lead(s)/project manager.
• Perform Query Management
• Define specifications and collaborate with technical team on configuration of centralized data management platform, elluminate® Data Central for data cleaning strategy and oversight activities.
• Prepare and maintain data management documentation (e.g., DMP, CCGs, Help Text, DVS) and update throughout trial lifecycle.
• Review and ensure the quality control of team-developed deliverables, covering eCRFs, study documents, program/report specifications, outputs, and elluminate® Data Central with analytics modules. Actively evaluate and contribute to enhance processes to increase efficiency and effectiveness.
• Collaborate and work as a team to ensure the deliverables are completed on time with high quality.
• Ensure compliance with industry quality standards, regulations, guidelines, and procedures.
• Other duties as assigned.
CANDIDATE’S PROFILE:
Education & Experience
• 5+ years’ experience in Clinical Data Management preferred.
• Bachelor’s degree in a health-related field or equivalent experience preferred.
• CCDM Certification preferred.
Professional Skills
• Strong project management experience and project team leadership skills including work planning, work delegation and solving complex problems.
• Strong analytical and strategic thinking skills
• Detail oriented, ability to multitask with strong prioritization, planning and organization skills.
• Excellent collaborative skills
• Demonstrated command of the English language with proficiency in both verbal and written communication
Technical Skills
• Proficiency in Microsoft Office Applications, specifically MS Project and MS Excel
• Knowledge of ICH/GCP guidelines, 21 CFR Part 11 and clinical trial methodology
• Proficient with EDC and Clinical Data Management Systems
• Experience with Cloud SaaS platforms (preferred)Experience with data reporting tools such as Qlik, JReview, Spotfire preferred.
• Experience with RBQM methodology preferred.
• Exposure to CDISC guidelines and standards
Clinical Data Manager
Posted today
Job Viewed
Job Description
Role: Associate Manager - Clinical Data Management
Location: Chennai, Tamil Nadu
Experience: 10+ Years
Requirements:
- 10-12 years of experience in clinical trial/data management and data operations.
- Minimum 4-5 years of people management (preferred) experience with proven supervisory
- skills.
- Extensive experience with CTMS platforms (CRIO, RT CTMS, Veeva Vault CTMS, or similar).
- Strong background in EDC systems management and clinical data operations.
- Experience in pharmaceutical, biotechnology, or CRO environment across multiple
- therapeutic areas.
Technical Expertise
- CTMS configuration and administration skills (Having knowledge in CRIO is an advantage).
- Deep knowledge of EDC platforms and system integrations.
- Strong understanding of regulatory requirements (HIPPA, FDA, EMA, ICH-GCP).
- Experience with electronic systems validation and 21 CFR Part 11 compliance.
Clinical Data Manager
Posted today
Job Viewed
Job Description
Experience: 5+ yrs
Work Mode: Work from Office
Work Location: Bangalore
LOOKING FOR IMMEDIATE JOINERS ONLY
Job Description - Clinical Data Manager :
OVERVIEW
The Clinical Data Manager (CDM) is an independent role responsible for supporting the study team and developing comprehensive study documentation, designing database specifications, and overseeing validation, maintenance/data cleaning, and closeout activities for clinical trial databases. The CDM is recognized as the platform expert, leveraging cutting-edge tools and technologies to provide continuous data insights and ensure the timely delivery of high-quality results for Sponsors. The CDM has a strong foundation in clinical data management, combined with the agility to adapt as processes evolve towards the integration of clinical data science.
KEY TASKS & RESPONSIBILITIES
• Define project specifications for Data Management services, including Protocol Conversion, Database Build, CRF Design and Data Review and Data Reconciliation tools.
• Understand external data collection, its integration into the clinical trial, and the management and reconciliation processes required to ensure its accuracy and relevance.
• Execute data cleaning strategies to accelerate the time to achieve subject data cleanliness and ensure high-quality, timely deliverables.
• Perform holistic data review and trending analysis via reporting and elluminate analytics to proactively identify issue, risks and develop mitigation strategies.
• Utilize artificial intelligence (AI) and machine learning (ML) for anomaly and outlier detection to enhance the efficiency and quality of trial data.
• Monitor and interpret key performance indicators (KPIs), metrics, dashboards, Clinical Trial Operational Analytics (CTOA), and reports to provide actionable recommendations to study lead(s)/project manager.
• Perform Query Management
• Define specifications and collaborate with technical team on configuration of centralized data management platform, elluminate Data Central for data cleaning strategy and oversight activities.
• Prepare and maintain data management documentation (e.g., DMP, CCGs, Help Text, DVS) and update throughout trial lifecycle.
• Review and ensure the quality control of team-developed deliverables, covering eCRFs, study documents, program/report specifications, outputs, and elluminate Data Central with analytics modules. Actively evaluate and contribute to enhance processes to increase efficiency and effectiveness.
• Collaborate and work as a team to ensure the deliverables are completed on time with high quality.
• Ensure compliance with industry quality standards, regulations, guidelines, and procedures.
• Other duties as assigned.
CANDIDATE’S PROFILE:
Education & Experience
• 5+ years’ experience in Clinical Data Management preferred.
• Bachelor’s degree in a health-related field or equivalent experience preferred.
• CCDM Certification preferred.
Professional Skills
• Strong project management experience and project team leadership skills including work planning, work delegation and solving complex problems.
• Strong analytical and strategic thinking skills
• Detail oriented, ability to multitask with strong prioritization, planning and organization skills.
• Excellent collaborative skills
• Demonstrated command of the English language with proficiency in both verbal and written communication
Technical Skills
• Proficiency in Microsoft Office Applications, specifically MS Project and MS Excel
• Knowledge of ICH/GCP guidelines, 21 CFR Part 11 and clinical trial methodology
• Proficient with EDC and Clinical Data Management Systems
• Experience with Cloud SaaS platforms (preferred)Experience with data reporting tools such as Qlik, JReview, Spotfire preferred.
• Experience with RBQM methodology preferred.
• Exposure to CDISC guidelines and standards
Clinical Trials Manager
Posted today
Job Viewed
Job Description
Clinical Trial Manager
Posted 6 days ago
Job Viewed
Job Description
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Clinical Data Manager
Posted 2 days ago
Job Viewed
Job Description
Location : Chennai, Tamil Nadu
Experience : 10+ Years
Requirements:
10-12 years of experience in clinical trial/data management and data operations.
Minimum 4-5 years of people management (preferred) experience with proven supervisory
skills.
Extensive experience with CTMS platforms (CRIO, RT CTMS, Veeva Vault CTMS, or similar).
Strong background in EDC systems management and clinical data operations.
Experience in pharmaceutical, biotechnology, or CRO environment across multiple
therapeutic areas.
Technical Expertise
CTMS configuration and administration skills (Having knowledge in CRIO is an advantage).
Deep knowledge of EDC platforms and system integrations.
Strong understanding of regulatory requirements (HIPPA, FDA, EMA, ICH-GCP).
Experience with electronic systems validation and 21 CFR Part 11 compliance.
Clinical Data Manager
Posted 4 days ago
Job Viewed
Job Description
Work Mode: Work from Office
Work Location: Bangalore
LOOKING FOR IMMEDIATE JOINERS ONLY
Job Description - Clinical Data Manager :
OVERVIEW
The Clinical Data Manager (CDM) is an independent role responsible for supporting the study team and developing comprehensive study documentation, designing database specifications, and overseeing validation, maintenance/data cleaning, and closeout activities for clinical trial databases. The CDM is recognized as the platform expert, leveraging cutting-edge tools and technologies to provide continuous data insights and ensure the timely delivery of high-quality results for Sponsors. The CDM has a strong foundation in clinical data management, combined with the agility to adapt as processes evolve towards the integration of clinical data science.
KEY TASKS & RESPONSIBILITIES
• Define project specifications for Data Management services, including Protocol Conversion, Database Build, CRF Design and Data Review and Data Reconciliation tools.
• Understand external data collection, its integration into the clinical trial, and the management and reconciliation processes required to ensure its accuracy and relevance.
• Execute data cleaning strategies to accelerate the time to achieve subject data cleanliness and ensure high-quality, timely deliverables.
• Perform holistic data review and trending analysis via reporting and elluminate® analytics to proactively identify issue, risks and develop mitigation strategies.
• Utilize artificial intelligence (AI) and machine learning (ML) for anomaly and outlier detection to enhance the efficiency and quality of trial data.
• Monitor and interpret key performance indicators (KPIs), metrics, dashboards, Clinical Trial Operational Analytics (CTOA), and reports to provide actionable recommendations to study lead(s)/project manager.
• Perform Query Management
• Define specifications and collaborate with technical team on configuration of centralized data management platform, elluminate® Data Central for data cleaning strategy and oversight activities.
• Prepare and maintain data management documentation (e.g., DMP, CCGs, Help Text, DVS) and update throughout trial lifecycle.
• Review and ensure the quality control of team-developed deliverables, covering eCRFs, study documents, program/report specifications, outputs, and elluminate® Data Central with analytics modules. Actively evaluate and contribute to enhance processes to increase efficiency and effectiveness.
• Collaborate and work as a team to ensure the deliverables are completed on time with high quality.
• Ensure compliance with industry quality standards, regulations, guidelines, and procedures.
• Other duties as assigned.
CANDIDATE’S PROFILE:
Education & Experience
• 5+ years’ experience in Clinical Data Management preferred.
• Bachelor’s degree in a health-related field or equivalent experience preferred.
• CCDM Certification preferred.
Professional Skills
• Strong project management experience and project team leadership skills including work planning, work delegation and solving complex problems.
• Strong analytical and strategic thinking skills
• Detail oriented, ability to multitask with strong prioritization, planning and organization skills.
• Excellent collaborative skills
• Demonstrated command of the English language with proficiency in both verbal and written communication
Technical Skills
• Proficiency in Microsoft Office Applications, specifically MS Project and MS Excel
• Knowledge of ICH/GCP guidelines, 21 CFR Part 11 and clinical trial methodology
• Proficient with EDC and Clinical Data Management Systems
• Experience with Cloud SaaS platforms (preferred)Experience with data reporting tools such as Qlik, JReview, Spotfire preferred.
• Experience with RBQM methodology preferred.
• Exposure to CDISC guidelines and standards
Clinical Data Manager
Posted today
Job Viewed
Job Description
Experience: 5+ yrs
Work Mode: Work from Office
Work Location: Bangalore
LOOKING FOR IMMEDIATE JOINERS ONLY
Job Description - Clinical Data Manager :
OVERVIEW
The Clinical Data Manager (CDM) is an independent role responsible for supporting the study team and developing comprehensive study documentation, designing database specifications, and overseeing validation, maintenance/data cleaning, and closeout activities for clinical trial databases. The CDM is recognized as the platform expert, leveraging cutting-edge tools and technologies to provide continuous data insights and ensure the timely delivery of high-quality results for Sponsors. The CDM has a strong foundation in clinical data management, combined with the agility to adapt as processes evolve towards the integration of clinical data science.
KEY TASKS & RESPONSIBILITIES
• Define project specifications for Data Management services, including Protocol Conversion, Database Build, CRF Design and Data Review and Data Reconciliation tools.
• Understand external data collection, its integration into the clinical trial, and the management and reconciliation processes required to ensure its accuracy and relevance.
• Execute data cleaning strategies to accelerate the time to achieve subject data cleanliness and ensure high-quality, timely deliverables.
• Perform holistic data review and trending analysis via reporting and elluminate® analytics to proactively identify issue, risks and develop mitigation strategies.
• Utilize artificial intelligence (AI) and machine learning (ML) for anomaly and outlier detection to enhance the efficiency and quality of trial data.
• Monitor and interpret key performance indicators (KPIs), metrics, dashboards, Clinical Trial Operational Analytics (CTOA), and reports to provide actionable recommendations to study lead(s)/project manager.
• Perform Query Management
• Define specifications and collaborate with technical team on configuration of centralized data management platform, elluminate® Data Central for data cleaning strategy and oversight activities.
• Prepare and maintain data management documentation (e.g., DMP, CCGs, Help Text, DVS) and update throughout trial lifecycle.
• Review and ensure the quality control of team-developed deliverables, covering eCRFs, study documents, program/report specifications, outputs, and elluminate® Data Central with analytics modules. Actively evaluate and contribute to enhance processes to increase efficiency and effectiveness.
• Collaborate and work as a team to ensure the deliverables are completed on time with high quality.
• Ensure compliance with industry quality standards, regulations, guidelines, and procedures.
• Other duties as assigned.
CANDIDATE’S PROFILE:
Education & Experience
• 5+ years’ experience in Clinical Data Management preferred.
• Bachelor’s degree in a health-related field or equivalent experience preferred.
• CCDM Certification preferred.
Professional Skills
• Strong project management experience and project team leadership skills including work planning, work delegation and solving complex problems.
• Strong analytical and strategic thinking skills
• Detail oriented, ability to multitask with strong prioritization, planning and organization skills.
• Excellent collaborative skills
• Demonstrated command of the English language with proficiency in both verbal and written communication
Technical Skills
• Proficiency in Microsoft Office Applications, specifically MS Project and MS Excel
• Knowledge of ICH/GCP guidelines, 21 CFR Part 11 and clinical trial methodology
• Proficient with EDC and Clinical Data Management Systems
• Experience with Cloud SaaS platforms (preferred)Experience with data reporting tools such as Qlik, JReview, Spotfire preferred.
• Experience with RBQM methodology preferred.
• Exposure to CDISC guidelines and standards