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2.0 - 5.0 years
3 - 7 Lacs
mumbai
Work from Office
ICON Strategic Solutions is looking for SCRA to join our team Roles and Responsibility Develop and implement comprehensive financial models to analyze market trends and predict future growth. Conduct thorough risk assessments and provide recommendations to mitigate potential risks. Collaborate with cross-functional teams to identify and capitalize on new business opportunities. Analyze complex data sets to extract insights that inform strategic decisions. Design and execute investment strategies aligned with client objectives. Provide expert advice and guidance to clients on investment planning and portfolio management. Job Requirements Strong understanding of financial markets, instruments,...
Posted 17 hours ago
1.0 - 3.0 years
3 - 7 Lacs
mumbai
Work from Office
IQVIA Biotech is looking for Clinical Research Coordinator to join our team Conduct site/trial feasibility to identify and select the right sites and investigators for studies. Ensure timely compilation of all essential documents and assist in regulatory package preparation. Coordinate with sites for study initiation, review patient data base, pre-screening, and identify physician networks. Manage clinical trial supplies receipt, accountability, storage, dispensing, and related documentation. Prepare site teams for study initiation visits and coordinate with monitors for the visit. Assist in administering informed consent and discuss patient information sheets in detail. Maintain current, ac...
Posted 2 days ago
1.0 - 3.0 years
3 - 7 Lacs
mumbai
Work from Office
Conduct site/trial feasibility to identify and select the right sites and investigators for studies. Ensure timely compilation of all essential documents and assist in regulatory package preparation. Coordinate with sites for study initiation, review patient data base, pre-screening, and identify physician networks. Manage clinical trial supplies receipt, accountability, storage, dispensing, and related documentation. Prepare site teams for study initiation visits and coordinate with monitors for these visits. Assist in administering informed consent and discussing patient information sheets with potential objects. Maintain current, accurate, and complete site documentation. Coordinate lab s...
Posted 1 week ago
1.0 - 3.0 years
2 - 5 Lacs
lucknow
Work from Office
Medblue Innovations Private Limited is looking for Clinical Trial Coordinator to join our dynamic team and embark on a rewarding career journey We are looking for highly motivated and experienced Clinical Trial Coordinators to join our team at Medblue Innovations Private Limited. The ideal candidate will have a strong background in clinical trials and excellent coordination skills. Roles and Responsibility Coordinate and manage clinical trial activities, including site initiation, monitoring, and close-out visits. Develop and maintain relationships with investigators, sites, and other stakeholders to ensure successful study execution. Manage study timelines, budgets, and resources to meet pr...
Posted 1 week ago
1.0 - 3.0 years
3 - 6 Lacs
lucknow
Work from Office
We are looking for highly motivated and experienced Clinical Trial Coordinators to join our team at Medblue Innovations Private Limited. The ideal candidate will have a strong background in clinical trials and excellent coordination skills. Roles and Responsibility Coordinate and manage clinical trial activities, including site initiation, monitoring, and close-out visits. Develop and maintain relationships with investigators, sites, and other stakeholders to ensure successful study execution. Prepare and review study protocols, informed consent forms, and other study-related documents. Ensure compliance with regulatory requirements and company policies. Collaborate with cross-functional tea...
Posted 1 week ago
1.0 - 3.0 years
3 - 6 Lacs
lucknow
Work from Office
We are looking for highly motivated and experienced Clinical Trial Coordinators to join our team at Medblue Innovations Private Limited. The ideal candidate will have a strong background in clinical trials and excellent coordination skills. Roles and Responsibility Coordinate and manage clinical trial activities, including site initiation, monitoring, and close-out visits. Develop and maintain relationships with investigators, sites, and other stakeholders to ensure successful study execution. Manage study timelines, budgets, and resources to achieve project goals. Ensure compliance with regulatory requirements and company policies. Collaborate with cross-functional teams to resolve issues a...
Posted 1 week ago
1.0 - 3.0 years
3 - 6 Lacs
lucknow
Work from Office
Medblue Innovations Private Limited is looking for Clinical Trial Coordinator to join our dynamic team and embark on a rewarding career journey Coordinate day-to-day operations of clinical trials, ensuring adherence to protocols. Communicate with investigators, sponsors, and regulatory bodies to ensure compliance. Manage trial logistics, including scheduling, data collection, and patient recruitment. Monitor trial progress and report any deviations or issues. Ensure accurate documentation and data entry for all trial-related activities. Provide support to the clinical team and ensure smooth trial execution. Disclaimer: This job description has been sourced from a public domain and may have b...
Posted 1 month ago
0.0 - 3.0 years
2 - 4 Lacs
mumbai
Work from Office
Concept Pharmaceuticals Ltd. is looking for Clinical Research Associate to join our dynamic team and embark on a rewarding career journey As a Clinical Research Associate (CRA), you will be responsible for monitoring clinical trials and ensuring that they are conducted in accordance with regulatory requirements and ethical standards Ensure compliance with study protocols, regulatory requirements, and ethical standardsMonitor and review study data to ensure accuracy, completeness, and compliance with study protocolsStrong knowledge of clinical research protocols, regulations, and guidelines, including ICH-GCP and FDA regulations Proficiency in using clinical research software, such as EDC sys...
Posted 2 months ago
5.0 - 10.0 years
8 - 12 Lacs
Nagpur
Work from Office
5 yrs experience on global clinical trials, including CRC CRA experience Having CRA team management experience must JD: Offer handholding to CRC's, stie start up specialist for activities like identifying potential doctors to close out of the trial from end to end all trial conduct activities Onsite visit for purpose of SIV, IMV, Close out visit, any audits by stakeholders Market research of feasible hospitals Area: Nagpur, Raipur, Aurangabad, Pune
Posted 5 months ago
2.0 - 7.0 years
3 - 7 Lacs
Nagpur
Work from Office
2 yrs CRC experience/ Bpharm, Mpharm/Bpharm,MBA qualification, fresher or intern in any pharmaceutical marketing/ Worked as Placement Coordinator for pharmacy college, Good Communication, Interpersonal analytical skills , establish Relationship with colleges, their placement cell, faculties, managing relationship with hospitals Doctors/investigators, handling grievance, helping out MD of company for developing patient data base, handling placement Drive event related things, establish follow up communication with CRO's/ Sponsor/hospitals IT companies regarding same.
Posted 5 months ago
7.0 - 11.0 years
9 - 13 Lacs
Bengaluru
Work from Office
Skill required: Clinical Data Services - Clinical Data Management Designation: Clinical Data Svs Specialist Qualifications: Bachelor of Pharmacy Years of Experience: 7 to 11 years What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the world's leading biopharma companies bring their vision to life - enabling them to improve outcomes by converging around the pa...
Posted 6 months ago
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