Current jobs related to Clinical Trial Associate - Mumbai Maharashtra - Atnahs

  • Clinical Research Associate

    3 days ago

    Mumbai, Maharashtra, India ClinoGenesis Research Institute Full time

    Clinical Research Associate (Interns / Freshers) **Pre-Trial**: - Identify and qualify potential clinical trial sites and investigators. - Set up and equip trial sites with the necessary materials and equipment. - Train site staff on study procedures and data collection methods. - Develop and maintain study manuals and documentation. **Monitoring**: -...

  • Clinical Trials Documentation Specialist

    5 hours ago

    Mumbai, Maharashtra, India beBeeDocumentManagement Full time ₹ 1,04,000 - ₹ 1,30,878

    Senior TMF Associate Job Summary">The Senior TMF Associate plays a key role in ensuring the smooth management of clinical trials documentation.This individual will be responsible for managing document classification, review, and deletion processes under Smart Inbox and ARC. They will ensure that all clinical study documents are uploaded, classified, and...

  • Clinical Research Associate

    15 hours ago

    Navi Mumbai, Maharashtra, India OMH HealthEdge Holdings Full time

    Vasta Bio-Informatics Private LimitedMaharashtraPosted On - 04 Oct 2024 - Required Experience - 1 - 3 Years Basic SectionNo. Of Openings 1 Grade C1B Designation CLINICAL RESEARCH ASSOCIATE Closing Date 29 Nov 2024 - OrganisationalCountry IN State MAHARASHTRA City NAVI MUMBAI Location Navi Mumbai-I - SkillsSkill CLINICAL...

  • Clinical Trial Assistant- I

    15 hours ago

    Karve Nagar, Pune, Maharashtra, India ProRelix Research Full time

    **Immediate Joiner** **Job Summary**: We are seeking a highly motivated and detail-oriented Clinical Trial Assistant (CTA) - I to join our clinical operations team. The CTA will support the execution of clinical trials by providing administrative and coordination assistance. This is an entry-level position ideal for recent graduates or those with up to 6...

  • Clinical Research Associate

    4 days ago

    Mumbai, Maharashtra, India Sun Pharma Laboratories Ltd Full time

    **Title**:Clinical Research Associate**: - Date: Sep 3, 2024- Location: Sun House - Corporate Office- Company: Sun Pharma Laboratories Ltd**In-House Managed Studies** - Site feasibility, potential investigator identification and development of study budgets for each study - Finalization of investigators, sites and execution of CDA and study related...

  • Clinical Research Associate

    15 hours ago

    Mumbai, India Statistical Pharma Full time

    Specific duties can vary depending on the company, but clinical research associates will generally be required to: - Develop trial procedures, methodology and instructions for clinical trials staff, as well as design data collection tools (case report forms) - Manage study supplies, drug supplies and drug accountability (and prepare study drugs for...

  • Trial Design Associate

    15 hours ago

    Mumbai, India OneStudyTeam Full time

    At OneStudyTeam (a Reify Health company), we specialize in speeding up clinical trials and increasing the chance of new therapies being approved with the ultimate goal of improving patient outcomes. Our cloud-based platform, StudyTeam, brings research site workflows online and enables sites, sponsors, and other key stakeholders to work together more...

  • Clinical Trial Assistant

    4 days ago

    Mumbai, India Life Force Homeopathy Full time

    Responsible for writing and managing protocols, recruitment, patient screening, patient consent forms and follow up management with Investigator. - Maintain source documentation and drug accountability, AE/SAEs reporting, maintaining site master file. - Site monitoring, Inspection, Audit etc. - **Development of study documents for and Management of...

  • Clinical Trial Administrator

    15 hours ago

    Navi Mumbai, India Labcorp Full time

    **Essential Job Duties**: 1) Document and track study activities using relevant forms and tools, as well as relevant Project Management Systems with guidance/support 2) Assist in the preparation of study and site specific materials in accordance with relevant SOPs 3) Complete minute taking and documentation for sponsor/external or internal teleconferences...

  • Manager-Biologics Regulatory Affairs(Clinical Trials)

    4 days ago

    Mumbai, Maharashtra, India USV PRIVATE LIMITED Full time

    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: BiologicsPosition: 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...

Clinical Trial Associate

2 weeks ago

Mumbai Maharashtra, India Atnahs Full time

**Mumbai or Vadodara, India (hybrid: 3 days office, 2 days home)**:
**Salary: Competitive + Benefits + Bonus**:
If you are an agile, committed, and innovative clinical trial professional, then we want to hear from you

Join us to help improve peoples’ lives and make healthcare better for everyone

**Why Pharmanovia?**:
Pharmanovia is a dynamic, fast-growing international pharmaceutical company with a portfolio of over 20 brands across more than 160 markets. Our mission is to improve patient health globally through the revitalisation of niche, tried-and-trusted medicines.

**Our core behaviours are**:

- We act decisively but we never compromise on quality.
- We keep our promises and do as we say.
- We value our heritage and foster an entrepreneurial spirit.
- We reinvest in our future - in our products, our brands and our people.
- We give back to our communities.

Since its inception in 2013, Pharmanovia has grown consistently year on year, focusing on delivering high-quality branded prescription medicines to patients, prescribers, and healthcare providers across the world. Our growth has enabled the company to reinvest in its products, brands, people, and to give back to its communities. A people business with a strong, supportive culture that encourages innovation and entrepreneurial spirit, our team comprises over 300 employees and 29 nationalities, operating from offices in the UK, Denmark, Netherlands, Switzerland, U.A.E., India, Singapore, Italy, Spain, and South Korea.

We are an agile, committed, and innovative global specialty pharma business and a preferred partner for innovator pharma companies, instigating a paradigm shift in the life cycle management of iconic medicines. We seek to extensively engage with clinical communities to communicate product improvements and prioritise environmental, social, and governance considerations across the business and workforce.

Pharmanovia’s therapeutic areas include Cardiovascular, Oncology, Endocrinology and Neurology.

**About the role**:
As Clinical Trial Associate you will support the Clinical Trial Manager and Real-World Evidence Trial Manager in the effective documentation and coordination of logístical aspects of assigned trials, and act as a pivotal point of contact and support for the trial team.

Reporting to the Head of Clinical Development, you will take a leading role in the creation and maintenance of study documents. In addition, this is an important role in supporting the development and maintenance of the Clinical Quality Management System ensuring SOPs, policies, manuals and staff training records are kept complete and up-to-date, and that the QMS reflects current and best practice.

Our Clinical Development Department has an ethos of continuous improvement, refining systems and creating efficiencies. This, along with the rapid growth of the business, leads to a varied and dynamic working environment.

**Main responsibilities & duties**:

- Responsibility for ensuring that the Sponsor Oversight File (SOF) and/or the Trial Master File (TMF), to include electronic TMFs, is complete and accurate on an ongoing basis and ready for archiving according to timelines
- Performing/overseeing periodic QC of SOFs and/or TMFs at Pharmanovia to ensure completeness and accuracy
- Performing QC of any TMF maintained by Service Providers (SPs) during and at the end of a study as well as an evaluation of the SPs TMF processes before study initiation
- Maintaining and updating any electronic study folders to ensure eFiles reflect any paper TMF/SOF and vice versa
- Support with clinical archiving to ensure timely coordination of archiving study documentation.
- Arranging and participating in the organisation of Investigator Meetings & Study Team Meetings (internal and external), preparing agendas and taking (where appropriate) and distributing minutes as required
- Coordinating any study document reviews where required
- Assisting with the Ethics submissions; keep a track of submissions & approvals for the study. Liaise with Regulatory Affairs to ensure linkage with regulatory approvals
- Printing, distributing, and tracking of any study specific documents internally and to any SPs
- Creating and maintaining study contact lists and relevant information databases for study team
- Sending out Study Newsletters / Study Correspondence to all participating SPs/sites on an ongoing basis
- Facilitating and tracking any study payments following the internal approval process
- Facilitating the obtaining and maintenance of study insurances
- Conduct oneself at all times in accordance with Pharmanovia Quality Management System, company working practices and policies, applicable GxP regulations ensuring training in these areas is kept up to date at all times
- Assisting with the company’s Clinical Quality Management System:

- Reviewing, updating, and expanding Standard Operating Procedures and associated documents, policies, and manuals
- Ensuring staff are awa