ProductLife Group | Clinical Trial Officer | india
2 weeks ago
We are looking for an CTA Officer to take care of our existing projects which would include the following responsibilities:
Responsibility:
Operational Activity:
Preparation and submission of CTA in EU and outside of EU from initial CTA preparation until notification of results
Review of documents (clinical study protocol, Informed consent form, …)
Capacity to provide the technical/practical regulatory expertise on the documents and on submission strategy
Coordinator Back-up
Required education:
Scientific background
Required experience :
5 to 10 years
Required languages:
French if possible
Required technical skills:
Good overview of Clinical Trials environment
Skills of Clinical Trials regulation
CTA management through CTIS / Transition management
Experience in coordination of team
Word/excel/powerpoint
Meeting management
Additional experience and/or skills:
eTMF : Veeva
Force of proposal, good analysis of situation, proactivity
Good relationship
A plus if skills for the following countries: Japan, China, US, Canada
- Capacity to manage multiple activities in same time
-
Clinical Trial Officer
2 weeks ago
India ProductLife Group Full timeWe are looking for an CTA Officer to take care of our existing projects which would include the following responsibilities: Responsibility: Operational Activity: Preparation and submission of CTA in EU and outside of EU from initial CTA preparation until notification of results Review of documents (clinical study protocol, Informed consent form, …) ...
-
Clinical Trial Officer
1 week ago
India ProductLife Group Full timeWe are looking for an CTA Officer to take care of our existing projects which would include the following responsibilities: Responsibility: Operational Activity: Preparation and submission of CTA in EU and outside of EU from initial CTA preparation until notification of results Review of documents (clinical study protocol, Informed consent form,...
-
Clinical Trial Officer
2 weeks ago
India ProductLife Group Full timeWe are looking for an CTA Officer to take care of our existing projects which would include the following responsibilities:Responsibility:Operational Activity:Preparation and submission of CTA in EU and outside of EU from initial CTA preparation until notification of resultsReview of documents (clinical study protocol, Informed consent form, …)Capacity to...
-
ProductLife Group | HR Officer | india
2 weeks ago
india ProductLife Group Full timeThe role includes full spectrum HR Service delivery expertise through HR operations, policy admin, payroll and benefits admin and managing day to day employee queries and delivery of data analytics and reporting.Main activitiesAt a High level, the role responsibility includes full spectrum HR Service delivery expertise through HR operations, policy admin,...
-
ProductLife Group | HR Officer | india
2 weeks ago
india ProductLife Group Full timeThe role includes full spectrum HR Service delivery expertise through HR operations, policy admin, payroll and benefits admin and managing day to day employee queries and delivery of data analytics and reporting. Main activities At a High level, the role responsibility includes full spectrum HR Service delivery expertise through HR operations, policy admin,...
-
india ProductLife Group Full timeThe Medical Information Specialist is responsible for providing technical and scientific information to healthcare professionals, consumers, and internal staff on a wide range of pharmaceutical medicines, OTCs, medical devices and therapeutic areas, including conducting complex literature searches and reviews using various medical database. Also responsible...
-
india ProductLife Group Full timeThe Medical Information Specialist is responsible for providing technical and scientific information to healthcare professionals, consumers, and internal staff on a wide range of pharmaceutical medicines, OTCs, medical devices and therapeutic areas, including conducting complex literature searches and reviews using various medical database. Also responsible...
-
Data Analyst
2 weeks ago
India SIRO Clinpharm Pvt. Ltd. Full timeWe are seeking a Data Analyst - Clinical Trials to join our team at SIRO Clinpharm Pvt. Ltd.Job DescriptionA Data Analyst - Clinical Trials will be responsible for providing statistical support to clinical trials, including data analysis and reporting.About the RoleSalary: ₹12,50,000 per annum (estimated)Responsibilities:Providing statistical support to...
-
Medical Information Specialist
4 weeks ago
India ProductLife Group Full timeJob Overview:The Medical Information Specialist is a critical role within the ProductLife Group, responsible for delivering accurate and timely medical information to healthcare professionals, consumers, and internal staff. This includes conducting complex literature searches, reporting adverse events, and adhering to internal SOPs, client requirements,...
-
Legal Counsel
4 weeks ago
india George Clinical Full timeAn exciting new role has arisen within our growing legal team in India for an immediate start! The Legal Counsel at George Clinical is responsible for supporting the Group General Counsel in the provision of legal and strategic advice to the George Clinical group of companies, to ensure compliance with global laws, internal policies and corporate governance...
-
Legal Counsel
4 weeks ago
India George Clinical Full timeAn exciting new role has arisen within our growing legal team in India for an immediate start! The Legal Counsel at George Clinical is responsible for supporting the Group General Counsel in the provision of legal and strategic advice to the George Clinical group of companies, to ensure compliance with global laws, internal policies and corporate...
-
Expert Full Stack Developer for Clinical Trials
2 weeks ago
India TRYAL, Inc. Full timeCompany OverviewTryal, Inc. is a cutting-edge clinical software startup revolutionizing the world of clinical trials. Our agile, product-focused approach enables us to deliver innovative solutions empowering researchers and medical professionals to make faster, data-driven decisions that improve research outcomes.
-
MS CLINICAL RESEARCH | Sales Executive – NGS
3 days ago
india MS CLINICAL RESEARCH Full timeJob Title: Sales Executive – NGS (Next-Generation Sequencing)Company: MS Clinical Research Pvt LtdAbout Us:MS Clinical Research (MSCR) is a dynamic and forward-thinking clinical research organization dedicated to conducting cutting-edge clinical trials. We are committed to advancing medical science and contributing to the development of innovative...
-
Manager Clinical Affairs
4 weeks ago
india Medical Learning Hub Full timeClinical Affairs ManagerJoin the Future of HealthcareTC4A, a pioneer in democratizing healthcare innovations, is revolutionizing diagnostics with LightAI. We are seeking talented individuals to join our office in Noida and address one of healthcare’s biggest challenges, the overuse of antibiotics that leads to drug-resistant infections and costs billions...
-
Manager Clinical Affairs
3 weeks ago
India Medical Learning Hub Full timeClinical Affairs Manager Join the Future of Healthcare TC4A, a pioneer in democratizing healthcare innovations, is revolutionizing diagnostics with LightAI. We are seeking talented individuals to join our office in Noida and address one of healthcare’s biggest challenges, the overuse of antibiotics that leads to drug-resistant infections and costs...
-
Clinical Programmer/clinical Database Programmer
6 months ago
India Cytel, India Full timeAt Cytel, we work hard to create successful careers with significant professional growth for our employees, as a result of which they work hard to make Cytel successful. Cytel is a place where talent, experience and integrity come together to advance the state of clinical development. Clinical Programming Analyst is responsible for contributing to the...
-
Senior Global trial Manager
2 months ago
india Bristol Myers Squibb Full timeDesignation: Senior Global Trial maangerExperience: 10-17YearsMandatory Skills: RWE, Phase IV, Project lead, Study lead, Clinical Project managementTrial Management experience in Phase 4/RWE/Late phase studies? (If the answer for this question YES, then we are need one or more of the below experiences):Trial Management experience in single country/regional...
-
Senior Global trial Manager
2 months ago
india Bristol Myers Squibb Full timeDesignation : Senior Global Trial maanger Experience: 10-17Years Mandatory Skills : RWE, Phase IV, Project lead, Study lead, Clinical Project management Trial Management experience in Phase 4/RWE/Late phase studies? (If the answer for this question YES, then we are need one or more of the below experiences): Trial Management experience in single...
-
india Advanced Clinical Full timeAdvanced Clinical is a clinical development and strategic resourcing organization committed to providing a better clinical experience across the drug development journey. Our goal is to improve the lives of all those touched by clinical research – approaching each opportunity with foresight, character, resilience and innovation. Based on decades of...
-
Trial Coordinator
6 months ago
India Rijk Zwaan Full time-India, Garakahalli Horticulture Bachelor | Master **How does your job as Trial coordinator at Rijk Zwaan look like?**: As Trial coordinator you fulfill an essential role in developing pre-commercial trials network in the relevant growing areas in India in consultation with breeders and RZ’s commercial partners. For this, you are in close contact with the...