100 Clinical Trials jobs in India
Clinical Trials Coordinator
Posted today
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Healthcare Professional Needed for Clinical Trial Screening Interviews
We are seeking a skilled healthcare professional to collaborate with our team on clinical trial screening interviews. The ideal candidate will have experience in conducting interviews and possess excellent communication skills.
Job Description:
- Contact candidates within 48 hours of them volunteering on our platform.
- Conduct interviews based on a provided script.
- Receive paid training on specific studies during the training sessions.
Required Skills and Qualifications:
- Proficient in Urdu.
- Excellent communication and interpersonal skills.
- Able to work independently and as part of a team.
- Strong attention to detail and ability to follow instructions.
Benefits:
- Paid training sessions.
- Ongoing support and feedback from our team.
- The opportunity to work on various clinical trials and gain valuable experience.
Project Details:
- Location: India.
- Time commitment: minimum 3 hours per day (Monday through Friday).
- Duration: varies depending on the specific study requirements.
Additional Information:
- Varying workload.
Clinical Trials Assistant
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Chris O’Brien Lifehouse is an internationally recognised independent, not-for-profit cancer hospital leading the way in delivering patient-centred cancer care. We seek passionate, caring, and dedicated staff who align with our Founder’s vision of creating a collaborative environment in which, respect, discovery, empowerment, and nurture, thrive in the interests of our patients.
About the role:
The Clinical Trial Assistant in the Clinical Trial Oncology Unit will play a vital role in supporting the operational and administrative aspects of clinical trials. This position involves assisting with laboratory tasks, managing data, and ensuring compliance with study protocols and regulatory requirements.
- Provide administrative and operational support for clinical trials, ensuring adherence to timelines and study protocols.
- Assist in the collection, labelling, processing, and storage of biological samples (e.g., blood, tissue, urine) in accordance with study requirements.
- Maintain and update clinical trial documentation, including case report forms, study logs, and regulatory files.
- Perform data entry, validation, and management tasks to ensure accuracy and completeness of trial data.
- Support the preparation, handling, and shipment of clinical trial specimens following regulatory guidelines.
- Coordinate with laboratory and clinical staff to facilitate seamless trial operations.
- Monitor and manage laboratory inventory, ensuring adequate supplies for ongoing studies.
- Adhere to Good Clinical Practice (GCP) and Good Laboratory Practice (GLP) guidelines.
- Assist in quality control and assurance activities to maintain the integrity of clinical trial processes.
- Participate in team meetings, training sessions, and site visits as required.
Essential Criteria:
- Bachelor’s degree scientific field (e.g., Biology, Medical Laboratory Science, Biotechnology) preferred.
- Strong organisational and multitasking skills with attention to detail.
- Excellent communication and interpersonal skills to collaborate with cross-functional teams.
- Ability to work in a fast-paced research environment and adapt to changing priorities.
- Proficiency in Microsoft Office applications and other relevant software.
- Evidence of immunisations to comply with the NSW Health Occupational Assessment, Screening & Vaccination against Specified Infectious Diseases Policy for a Category A position
Benefits
- Market competitive remuneration and benefits
- Fitness passport for you and your family
- Access to e-Learning programs
- Social and wellbeing events
- CBHS Corporate Health
- Workplace banking benefits
- Access EAP
Culture
We are committed to providing a working environment where everyone is valued, respected, and supported to progress. Our priority is to ensure culture, policies, and processes are truly inclusive and that no one is disadvantaged because of their Indigenous identity, gender, culture, disability, LGBTIQA+ identities, family and caring responsibilities, age, or religion.
We encourage everyone who meets the selection criteria and shares Chris O`Brien Lifehouse values to apply.
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Clinical Trials Administrator
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As part of the ACM Clinical Trails Study Support team this role supports both the Project Team and Clinical Trials Investigator sites from study set up through to study close out. Acts as a member of the Project Team to support all ongoing studies with tasks as needed, as defined by the Project Team or ACM client.
STATUS: Full Time
LOCATION: On-site
DEPARTMENT: Study Support
SCHEDULE: Monday - Friday
ATTRIBUTES
- Master’s degree in Bio-chemistry, Microbiology or Chemistry preferred.
- 1 to 2 years’ experience in a similar capacity in a Central Laboratory or Contract Research Organisation.
- Excellent verbal and written communication skills required.
- Computer proficiency required; familiarity with relational databases and reporting tool strongly preferred.
- Ability to multi-task and prioritize workload required.
- Customer Service experience required.
- Critical thinking and ability to problem-solve.
RESPONSIBILITIES
**Project Set-up.** Coordinates internally to set-up assigned projects in LIMS. Complete and submit patient report, custom flagging, and requisition request forms Requisitions. Kit Order Manager (KOM) setup (including inventory notification to logistics) and QC and validation. QC of Protocol set-up summaries in each LIMS environment. QC of requisitions set-up in each environment. Validate the LIMS Protocol Set-up
**Logistics and Administration**. Manage inventory of supplies of kit components for phlebotomy kit assembly by liaising internally with logistics and with vendors who supply kit components. Liaison and interface with appointed logistic agency for supply of phlebotomy kits to investigator sites. Draft out logistic documents required to be submitted to logistic agency for transport. Interfaces with regional/reference/affiliate laboratory’s CT Specimen Processing, Project and Data Management departments to ensure prompt turnaround of all specimen analysis, lab reports as well as pending lab reports. Participates and documents Quality Audits and inspections of Clinical Trials as prescribed by departmental policies
**Benefits**:
- Life insurance
Schedule:
- Day shift
- Monday to Friday
Ability to commute/relocate:
- Mumbai Suburban, Maharashtra: Reliably commute or planning to relocate before starting work (required)
**Experience**:
- total work: 1 year (preferred)
Work Location: One location
- Health insurance
Manager-Biologics Regulatory Affairs(Clinical Trials)
Posted 4 days ago
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About USV Private Limited:
USV, a top-15 pharmaceutical company in India, excels in the diabetes and cardio sectors and has presence in over 65 countries.
Function: Biologics
Position: Asst Manager / Manager - Regulatory Affairs (Clinical Trials) For EU and US.
Job Location: Govandi (East ), Mumbai (1st, 3rd, 5th Saturday working, 2nd and 4th Saturday off))
Desired Qualification: M.Pharm/B.Pharm
Desired Work Experience: 5-15 years in RA-Clinical Trials for EU and US markets.
Job Responsibilities:
1. Biosimilar Clinical Development Strategy, Clinical trials, injectables for EU and US markets.
2. Biosimilar Clinical design and Protocol development, review and finalization for EU and US markets.
3. Biosimilar Clinical Trial Application, Overview of clinical study conduct, Clinical Study report review and finalization for EU and US markets.
4. Biologics/Biosimilar Dossier Authoring, Review and Hands on experience in eCTD submissions for EU and US markets.
5. MOH Query response
6. Product Life cycle Management
7. RA support for Plant related QMS activities
Manager-Biologics Regulatory Affairs(Clinical Trials)
Posted 3 days ago
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Job Description
USV, a top-15 pharmaceutical company in India, excels in the diabetes and cardio sectors and has presence in over 65 countries.
Function: Biologics
Position: Asst Manager / Manager - Regulatory Affairs (Clinical Trials) For EU and US.
Job Location: Govandi (East ), Mumbai (1st, 3rd, 5th Saturday working, 2nd and 4th Saturday off))
Desired Qualification: M.Pharm/B.Pharm
Desired Work Experience: 5-15 years in RA-Clinical Trials for EU and US markets.
Job Responsibilities:
1. Biosimilar Clinical Development Strategy, Clinical trials, injectables for EU and US markets.
2. Biosimilar Clinical design and Protocol development, review and finalization for EU and US markets.
3. Biosimilar Clinical Trial Application, Overview of clinical study conduct, Clinical Study report review and finalization for EU and US markets.
4. Biologics/Biosimilar Dossier Authoring, Review and Hands on experience in eCTD submissions for EU and US markets.
5. MOH Query response
6. Product Life cycle Management
7. RA support for Plant related QMS activities
Manager-Biologics Regulatory Affairs(Clinical Trials)
Posted today
Job Viewed
Job Description
About USV Private Limited:
USV, a top-15 pharmaceutical company in India, excels in the diabetes and cardio sectors and has presence in over 65 countries.
Function: Biologics
Position: Asst Manager / Manager - Regulatory Affairs (Clinical Trials) For EU and US.
Job Location: Govandi (East ), Mumbai (1st, 3rd, 5th Saturday working, 2nd and 4th Saturday off))
Desired Qualification: M.Pharm/B.Pharm
Desired Work Experience: 5-15 years in RA-Clinical Trials for EU and US markets.
Job Responsibilities:
1. Biosimilar Clinical Development Strategy, Clinical trials, injectables for EU and US markets.
2. Biosimilar Clinical design and Protocol development, review and finalization for EU and US markets.
3. Biosimilar Clinical Trial Application, Overview of clinical study conduct, Clinical Study report review and finalization for EU and US markets.
4. Biologics/Biosimilar Dossier Authoring, Review and Hands on experience in eCTD submissions for EU and US markets.
5. MOH Query response
6. Product Life cycle Management
7. RA support for Plant related QMS activities
Project Leadership – Biotech (Clinical Trials) - Obesity / Diabetes - Home Based (Future Needs)
Posted today
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When our values align, there's no limit to what we can achieve.
The Project Leadership function at Parexel is a critical part of driving success for our clients and advancing clinical research projects. As a part of the Global Project Leadership organization, your work has a direct impact on the projects, teams, and clients you work with, while helping deliver projects to the benefit of the patients we serve.
Parexel’s defined Biotech Division offers opportunities for seasoned Project Management professionals with a strong background running global clinical trials in a variety of therapeutics. This group focuses specifically on Biotech clients and providing all areas of support to accommodate their unique needs. This is a great opportunity for those in the industry who prefer the flexibility, creatively and problem-solving mindset to successfully support this type of clients.
Parexel has upcoming future opportunities at the Project Leader (PM) and Senior Project Leader (SPM) level for candidates with experience leading obesity global studies.
Individuals selected for these roles will provide leadership to project teams and manage the day-to-day operations while striving to achieve operational excellence through on time delivery within budget and to the highest quality with the goal to exceed client expectations
Successful candidates possess an undergraduate degree in a clinical or health related field: advanced degree preferred, along with at minimum, 2+ years' experience leading Global Clinal Trials in Project Management within a CRO (preferred), Biotech or Pharma company. These positions also require experience in project scheduling, managing resources and budgets and coordinating team activities, as well as experience with the full clinical development process through regulatory submissions. Additional years of experience will be required for the more senior role of Senior Project Leader.
To excel in this role, flexibility, problem solving capabilities and strategic vision are qualities that propel our Project Leadership team member’s growth. In addition, you need to be detailed-oriented, computer proficient and possess superior interpersonal and organizational skills.
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
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Clinical Trials-Reputed Pharmacy Industry-Chennai, Tamil Nadu, India -3 Lakhs-Sonali
Posted today
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JOB DETAILS
1.Creating and writing trial protocols, and presenting these to steering committee.
2.Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial.
3.Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion.
4.Liaise with ethics committee regarding rights, safety and well-being of trial subjects.
5.Ordering, tracking, and managing IP and trial materials.
6.Overseeing and documenting IP dispensing, inventory and reconciliation.
7.Protecting subjects’ confidentiality, updating their information, and verifying IP has been dispensed and administered according to protocol.
8.Conducting regular site visits, coordinating project meetings and writing visit reports.
9.Implementing action plans for sites not meeting expectations.
10.Liaising with regulatory authorities.
11.Ensuring compliance with SOPs and local regulations, and ICH and GCP guidelines.
12.Other tasks and responsibilities as needed.
FUNCTIONAL AREA
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Clinical Research Medical Advisor
Posted today
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**Clinical Research Medical Advisor**:
India
**About the role**
Novartis is a pioneer in drug development with a robust pipeline across therapy areas. CRMAs work closely with Investigators and ensure scientific engagement with the Investigator community to drive our programs and trials across the globe.
Your responsibilities include, but are not limited to:
- Closely collaborates with the Trial Monitoring Organisation to ensure fast clinical trial start up, recruitment according to planned timelines, early identification of potential delays and robust recruitment mitigation plan. Co-own start-up phase and the recruitment plan for development clinical trials with the local TMO organization.
- Provides robust indication and protocol training to CRAs and CSEs, and other functions in the country as needed; Provide protocol, Risk management plan & disease training as appropriate, and externally at Investigator’s Meetings or scientific venues to support recruitment and trial awareness.
- Assess the clinical feasibility of implementing a clinical trial protocol based on regional/local medical practice using physician interviews, local databases (RWE, payer data, patient association feedback, etc.) and analysis of the competitive environment
- Provide medical/clinical assistance to TMO and site for IEC/IRB Interactions; Support Ministry of Health interaction (or local Board of Health) as required
- Support Regulatory Affairs, Health Economics, Drug safety and epidemiology and Medical Information with medical/clinical input as appropriate as this relates to global development clinical trials and NIBR PoC trials.
- Support planning, implementation and follow-up of regulatory agency inspections and internal audits
- Review and try to resolve local medical issues / questions and, if feasible, support TMO with recruitment/ operational issues that arise during the entire course of the study - if necessary support the discussion of issues to global teams.
- Perform local AE review for development compounds and provide general medical support for safety issues
**Commitment to Diversity & Inclusion**:
- We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve._
**Role Requirements**
- At least 3 Years clinical development experience in pharmaceutical industry
- Sound understanding of the overall clinical development and ICH/GCP
- Ability to manage a study from the medical/clinical perspective, and a demonstrated capability to problem solve and mediate complex clinical / medical / operational issues
- Agility to move fast across different therapeutic areas and indications
- Scientific degree (medical degree highly desirable); Trained in relevant aspects of clinical drug development including GCP,
- local regulatory requirements and data privacy laws. Subspecialty training desirable, but not required.
Why Novartis?
Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we
**Division**
Development
**Business Unit**
CLINICAL DEVELOPMENT & CMO GDD
**Work Location**
Mumbai
**Company/Legal Entity**
Nov Hltcr Shared Services Ind
**Functional Area**
Research & Development
**Job Type**
Full Time
**Employment Type**
Regular
**Shift Work**
No
**Early Talent**
No
Project Research Scientist (Non-medical)
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Qualifications and experience should be in the relevant discipline/field and from an institution of repute. Experience must have been gained after acquiring the minimum essential qualification. Meeting the essential qualification criteria does not guarantee selection.
Contact
Dr. Aswathy S.
HOD and Professor,
Department of Community Medicine,
School of Medicine, Kochi
Location School of Medicine, Kochi
Required Number 1
**Job Description**:
Participating and assisting in conducting and minuting all meetings related to the Project.
Scientific Coordination between different study sites engaged in this project
Conducting research audits and preparing audit reports.
Providing Statistical support and assistance to design research manuscripts.
Other duties as assigned from time to time by the PO.
**Place of work**: AIMS, Kochi India
The position requires local travel within the Ernakulum district and other sites in India.
**Qualifications Essential Qualifications**:
First Class Postgraduate degree with Three years of Experience
Experience
Preference will be given with prior exposure to Anthropology, Epidmeiology Public Health or any other Degree in Clinical Epidemiology research
Good Communication and Mangerial Skills.
Proficient knowledge in epidemiological studies (experience in NCD research is desirable).
Experience in conducting population studies, planning, and executing community studies, and intervention studies in the field of Public Health.
Knowledge of qualitative research and experience in conducting Focus Group Discussions (FGDs), In-Depth Interviews (IDIs), Key Informant Interviews (KIIs), etc.
Proficiency in Malayalam Language is essential.
5 original research publications.
**Age Limit**: Upper age limits up to 40 years (maybe relaxed).
Salary 56000 +20% HRA