ProductLife Group | Clinical Trial Officer | india

1 week ago


india ProductLife Group Full time

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


  • India ProductLife Group Full time

    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, …) ...


  • India ProductLife Group Full time

    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 resultsReview of documents (clinical study protocol, Informed consent form, …)Capacity to...


  • India ProductLife Group Full time

    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,...


  • india ProductLife Group Full time

    The 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 time

    The 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,...


  • india ProductLife Group Full time

    The 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 time

    The 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 time

    We 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...


  • India ProductLife Group Full time

    Job 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 time

    An 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...

  • Legal Counsel

    4 weeks ago


    india George Clinical Full time

    An 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...


  • india MS CLINICAL RESEARCH Full time

    Job 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...


  • India TRYAL, Inc. Full time

    Company 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.


  • india Medical Learning Hub Full time

    Clinical 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...


  • India Medical Learning Hub Full time

    Clinical 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...


  • India Cytel, India Full time

    At 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...


  • india Bristol Myers Squibb Full time

    Designation: 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...


  • india Bristol Myers Squibb Full time

    Designation : 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 time

    Advanced 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...