Clinical research associate Jobs in India
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Clinical research associate • India
Last updated: 8 hours ago
Location : Ahemadabad - Salary : CompetitiveType : PermanentMain Industry : Other Industries & Skills : LegalJob ID : 130518242Posted On : 17 May 2024 Department –.
Clinical Medical Regulatory (CMR).Do you...Show moreLast updated: 30+ days ago
Are you looking for a work environment where you can innovate, reach greater heights and collaborate with experts from a wide range of sectors? You want to join a world-class company and industry l...Show moreLast updated: 30+ days ago
At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need acr...Show moreLast updated: 1 day ago
Clinical Research Associate
IQVIAKolhapur, IN Work Experience : 3+ years of experience.Work location : Metro Cities / Any of IQVIA office location.Perform monitoring and site management work to ensure that sites are conducting the study(ies) and ...Show moreLast updated: 2 days ago
Associate Research Manager
Hansa Research GroupBangalore Urban, Karnataka, India Research skills development Proposal Writing : .Follow the pre-requisites for the proposal - Need for study, objective of study, decide the research approach and methodology, research design elements...Show moreLast updated: 17 days ago
- Promoted
Veeda Clinical Research - Associate - Legal
Veeda Clinical Research LtdAhmedabad, India Key Responsibilities : Legal Expertise & Documentation : - Minimum 3 to 4 years of experience in a corporate legal environment.Well-versed with court pr...Show moreLast updated: 30+ days ago
Research Assistant / Research Associate
Symbiosis Skills & Professional UniversityIndia STEM careers and the broader workforce.Job placement rates and sectors employing trained women.Long-term job retention among women in skilled roles.
Factors contributing to workforce dropout.Gender-...Show moreLast updated: 21 days ago
Clinical Research Associate
Dr Reddy's Laboratories LimitedHyderabad, Telangana, India We are seeking a dynamic independent and experienced Research Associate in Clinical Management for processing reviewing and receiving clinical data and records and from therapeutic groups as well a...Show moreLast updated: 24 days ago
- Promoted
Clinical Research Lead
Sanofi EUHYDERABAD, Telangana, India Hiring Manager : Head Scientific Communications.Travel required as per business need.Job type : Permanent, Full time.Sanofi Business Operations is an internal Sanofi resource organization based in In...Show moreLast updated: 4 days ago
Research Associate
ITC LimitedBangalore, Karnataka, India Duediligence studies such as stability studies and performance evaluation.Qualityevaluation : Analysis and sensorial evaluations of finished product.
Ensuredocumentation of prototype formulations raw...Show moreLast updated: 24 days ago
Research Associate I
myGworkMumbai, India This job is with S&P Global, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community.
Please do not contact the recruiter directly.About the Rol...Show moreLast updated: 4 days ago
Clinical Research Associate
TipTopJob.comAhemadabad, IndiaPermanent
Research Associate / Research Lead
Voice of Commons OfficialIndia Research Associate / Research Lead.About the RoleAt Voice of Commons, we welcome individuals who are passionate about leveraging their skills and creativity to advocate for the marginalized.If you ...Show moreLast updated: 20 days ago
Associate Operations Research
CAEBangaloreFull-time
- Promoted
Lead Clinical Research Associate
Tech ObserverPalakkad, IN Contract Research Organization (CRO) with a presence in over 20 countries, is currently hiring.Senior / Lead Clinical Research Associates (CRAs) and APM (Asst.
We are seeking candidates with 4+ years ...Show moreLast updated: 4 days ago
Research Associate- Clinical Bioanalytics
Dr. Reddy's LaboratoriesINDIA Each of our 24,000 plus employees comes to work every day for one collective purpose : to accelerate access to affordable and innovative medicines because.
We started in 1984 with a modest investment...Show moreLast updated: 30+ days ago
- Promoted
Research Associate
Mercom IndiaBengaluru, Karnataka, India Mercom India is a subsidiary of U.Mercom Capital Group, leading clean energy communication and consulting firm recognized worldwide for its expertise in renewable energy.
Mercom is widely recognized...Show moreLast updated: 30+ days ago
Sr. Clinical Research Associate (India)
AllucentChennai, TN, INQuick Apply
Clinical Research Associate Clinical Pharmacology
Jeevan Scientific Technology LimitedINDIA Clinical Research Associate Clinical Pharmacology.Clinical Research Associate Clinical Pharmacology.Volunteer registration and screening process.
Coordination with diagnostic laboratory for reports...Show moreLast updated: 30+ days ago
Clinical Research Associate- Udaipur
Indira IVFUdaipur JOB RESPONSIBILITIES •Recruit and enroll study participants.Input clinical research data into electronic data systems.Coordinate patient visits and procedures related to research.Act as a resource f...Show moreLast updated: 30+ days ago
- New!
Market Research Associate
Quanten MediaChennai, Tamil Nadu, India Research Associate to join our growing team.Your mission? To help us decode the future of entertainment.You’ll anchor studies that explore what resonates with audiences—setting up experiments, runn...Show moreLast updated: 8 hours ago
Experienced Clinical Research Associate
MEDPACENavi Mumbai, India Medpace is a full-service clinical contract research organization (CRO).We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries.Our mi...Show moreLast updated: 30+ days ago
- Promoted
Research Associate
Zeta-V Technology Solutions LtdPune, Maharashtra, India Our client delivers actionable insights to financial institutions globally through our comprehensive research studies.This is a full-time position based in Pune, India.
We are seeking an associate t...Show moreLast updated: 4 days ago
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Clinical Research Associate
IQVIAKolhapur, IN2 days ago
Job descriptionBachelor's Degree Degree in scientific discipline or health care preferred. Req Equivalent combination of education, training and experience may be accepted in lieu of degree. Some organizations require completion of CRA training program or prior monitoring experience. Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines). Good therapeutic and protocol knowledge as provided in company training. Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable). Written and verbal communication skills including good command of English language. Organizational and problem-solving skills. Effective time and financial management skills. Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
Project Role : CRA 2
Work Experience : 3+ years of experience
Work location : Metro Cities / Any of IQVIA office location
Work Mode : Hybrid
Job Overview
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
Essential Functions
- Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability.
- Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
- Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
- Ensure copies / originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements.
- Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
- Collaborate and liaise with study team members for project execution support as appropriate.
- If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
- If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.
Qualifications