Clinical Data Management jobs in Chennai, Tamil Nadu
- ICON PlcChennai, Tamil Nadu
- Prior experience or strong interest in clinical research.
- KNwledge of clinical trial processes, regulations, and guidelines.
- Navitas Life SciencesChennai, Tamil Nadu
- In-depth understanding of the clinical development process combined with knowledge of real world medicine to overcome the challenges of collecting quality data…
- View all Navitas Life Sciences jobs - Chennai, Tamil Nadu jobs
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View similar jobs with this employerAccentureChennai, Tamil Nadu- These operations involve collecting and analyzing data from clinical trials, healthcare providers, and patients.
- Years of Experience:1-3 Yrs.
- EXL ServiceChennai, Tamil Nadu
- Responsibilities: Basic clinical knowledge on conditions, clinical presentation, signs/symptoms, investigation and management.
- Siemens HealthineersChennai, Tamil Nadu
- O Engage with healthcare professionals in clinical settings to understand workflow requirements and clinical challenges.
- O Portfolio ‘Solution Show(s)’.
- Navitas Life SciencesChennai, Tamil Nadu
- Provide training to new data management personnel on data management processes and procedures.
- Provide training to new staff, study site and sponsor personnel…
- PfizerChennai, Tamil Nadu
- The Senior Associate, Central Monitor is responsible for ensuring the completeness, quality and integrity of the subject data in the clinical trial database…
- 247 HealthMedProThoraipakkam, Chennai, Tamil Nadu
- Attention to detail and accuracy in data management.
- Perform data trending, interpretation, and analysis of nursing and clinical processes.
- 247 HealthMedProThoraipakkam, Chennai, Tamil Nadu
- Attention to detail and accuracy in data management.
- Perform data trending, interpretation, and analysis of nursing and clinical processes.
- ICON PlcChennai, Tamil Nadu
- You will bring relevant clinical data science experience, along with the following qualifications and skills.
- Developing and validating statistical programming…
- Micro Therapeutic Research Labs Pvt. Ltd (MTRL)Chennai, Tamil Nadu
- Collaborate with cross-functional teams, including clinical research associates, data managers, and biostatisticians, to ensure the integrity and quality of…
View similar jobs with this employerAccentureChennai, Tamil Nadu- The person would require understanding of the strategic direction set by senior management as it relates to team goals.
- Years of Experience:7 to 11 years.
- ICON PlcChennai, Tamil Nadu
- Proven experience in clinical data management within the pharmaceutical or biotechnology industry.
- Collaborate closely with cross-functional teams, including…
- AccentureChennai, Tamil Nadu
- Years of Experience:0 to 1 years.
- The goal is to offer a range of healthcare options to insured individuals at negotiated rates.
- CognizantTamil Nadu
- Ability to advise on population health management and value-based care models that improve clinical and financial outcomes.
- EXL ServiceChennai, Tamil Nadu
- Review call quality issues on various parameters such as conversational skills, claims resolution, and voice quality.
- Project a professional manner and image.
Job Post Details
Clinical Trial Associate
Job details
Full job description
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
We are currently seeking a Clinical Trial Administrator to join our diverse and dynamic team. As a Clinical Trial Administrator at ICON, you will play a pivotal role in assisting with the design and analysis of clinical trials, interpreting complex medical data, and contributing to the advancement of inNvative treatments and therapies.
What you will be doing
- Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.
- Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.
- Support the preparation of study-related materials, such as informed consent forms and case report forms.
- Work with cross-functional teams to facilitate communication and ensure smooth trial execution.
- Contribute to the tracking and reporting of clinical trial metrics and milestones.
Your profile
- Bachelor's degree in a scientific or healthcare-related field.
- Prior experience or strong interest in clinical research.
- KNwledge of clinical trial processes, regulations, and guidelines.
- Excellent organizational and communication skills.
- Ability to work collaboratively in a fast-paced environment with attention to detail.
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request .
Are you a current ICON Employee?