...new data collection requirements in assigned studies and provide clinical input into the development of new and updated clinical Data... ...Health Care Professionals such as Pharmacists, Nurses, Medical doctors, or Dentists.
• relevant experience in areas such as Clinical...
About the Role
Clinical Project Manager
Location – Hyderabad #LI Hybrid
About the Role:
This role is responsible to Lead and manage a multidisciplinary cross functional Clinical Trial Team (CTT) (medical writing, statistics, data management, monitoring partner, drug...
...maintenance or in closeout phase or ongoing studies post primary database lock with the oversight of the LCTL/CTL, as assigned. Support the clinical protocol development process in collaboration with the CTL/Lead CTL and the Clinical program Leader (CPL): chip in to the development...
...About the role
Clinical Data Scientist
Location – Hyderabad/ Mumbai
About the Role:
Provide timely and professional ongoing management of Data Management deliverables and of clinical trial data with respect to cost, quality and timelines for all assigned trials...
...About the role
“150! Clinical scientific experts, globally, are part of Global Drug Development (GDD) team, working to ensure clinical trial data and regulatory reports are of highest quality throughout the life cycle of each program, across all disease areas. Be part of...
...Global Drug Development (GDD) organizations to apply the scientific knowledge of pharmacokinetics, pharmacodynamics, metabolism and clinical pharmacology in advancing the drug candidates from discovery and clinical development through approval and beyond. Novartis portfolio...
About the Role
Job Purpose
The Head of Operational Excellence, Clinical Development will be accountable for leading key strategic global operational excellence activities across the CD function. The role will support strategic planning and operational execution in partnership...
About the Role
Your responsibilities will include, but are not limited to:
• Represents GCS as a core member in the integrated Clinical Trial Team (iCTT); defines and advises the iCTT on the optimal clinical trial supply strategy in terms of, but not limited to, packaging...
General Medicine Job in Nizamabad
We have urgent requirement of general Medicine Job in Nizamabad.
Qualification : MBBS and MD/DNB (General medicine)
Experience : 0 to 10 years.
Salary : As per Experience.
Interested doctors please Apply
We Have urgent requirement of General Medicine opening near Hyderabad.
Qualification: MBBS and MD/DNB
Salary: 1,50,000 to 2,00,000 plus accommodation
Interested Doctors please apply.
Nagarjuna Consultancy Required Doctors for Telangana and Andhrapradesh
...We have urgent requirement of Internal Medicine Doctor jobs in Multiple Locations in Telangana.
Qualification: MBBS and MD/DNB Internal Medicine)
Experience: 0 to 20 years.
Locations: Hyderabad, Warangal, Nizamabad, Khammam, Karimnagar, Ramagundam, Mahabubnagar, Nalgonda...
...information thereto, so as to effectively communicate with the medical doctors and handle product related customer queries
- Utilize... ...campaigns as per Company s plans.
- Covers the Nursing homes, clinics and hospitals as per agreed coverage requirements.
- Assists...
...any crucial situation happened at site.
- Maintain cleanness in clinic with fennel and keep sanitizer for health precautions.
- Make... ...patient care with various health care team members
- Follow doctors rounds for assigned patients, and carry out doctor's orders and instructions...
...families.
- To effectively conduct and communicate routine and urgent nursing assessments effectively with our Healthcare clinical providers, including doctors, other nurses, and ancillary provider staff.
- To effectively coordinate patient care and referrals for doctors and...
About the Role
Responsible for contributing to the planning, coordination, development and timely delivery of high quality Clinical submission documents to Regulatory Affairs (RA) for
1) New Drug Applications (NDA), Biologic Licensing Applications (BLA), Marketing Authorization...
...relevant work instructions incl. financial risk controls (NFCM)
• Provide process/system expert support & training to all countries having clinical trial activities – Governance over RDF CoE future transitions, KPIs, projects, check-in NFCM controls.
• Support audit reporting...
...Independently manage and execute drug shipment ticket review process (US)
• In addition to regulatory manager, provide guidance to clinical functions on regulatory compliance activities, such as requirements for TOOs, VDRs, drug shipment etc.
• Assist regulatory managers...
...emotional and physical challenges that come with infertility.
Role Description
This is a full-time on-site role for a Junior Doctor at Ferty9 Fertility Center in Tirupati. The Junior Doctor will be responsible for providing direct patient care, including conducting...
...performance capability on various tasks and activities. They work day and night to achieve their targets. - Their foremost job is to meet doctors and health experts, get prescribed medicines, and generate sales in the market. They make the doctors fully aware of new pharma...
...Responsibilities: Development Data Team is responsible to design and execute data management strategy across Drug Development line functions i.e. Clinical Operations, Clinical Data Standards, Technical Research & Development, Regulatory Affairs and Patient Safety. Function also...
...company standards by providing input into CRF and data structures tables, listings and figures for Interventional and Non-Interventional Clinical studies.
Maintain efficient interfaces with other statisticians, internal and external customers, CROs and CPOs as needed.
Take...
About the Role
Your responsibilities include, but are not limited to:
• Provides scientific and medical expertise on assigned clinical projects. Contributes to clinical strategy for the Asian region.
• Accountable for all aspects related to wind down projects including...
...Biostatistician is responsible for all statistical work, scientific and operational, for one or more assigned trials in collaboration with the clinical trial team. May support project level deliverables for a development project with supervision.
Leads implementation of modern and...
...Novartis.
Key Responsibilities:
• Lead and coordinate activities of all statistical programmers as Trial Programmer for phase I to IV clinical studies or assigned project-level activities. Make statistical programming recommendations at study level.
• Build and maintain...
...tools that optimize the acquisition, storage, integration, mining, analysis, visualization, and interpretation of chemical, biological, clinical and operational data.
Key Responsibilities:
• Develop state-of-the-art software tools and methodologies to support the discovery...
...work environment and diverse teams representative of the patients and communities we serve.
Role Requirements
• 8 years relevant clinical trial operations experience, from technology or health care sector. General understanding of drug development – early development, clinical...
...programming specifications for analysis datasets and pooled datasets for a project.
• Lead the production of statistical outputs for clinical study reports, publications, and market promotions. Ensure the quality control of all programs, specifications and statistical...
...partners and cross-functional teams to solve critical business problems. Understand life science data sources including preclinical, clinical, sales, contracting, promotions, social media, patient claims and Real-World Evidence
• Research and co-develop with supervisor in...
...About the role
The Senior Study Leader is responsible for the execution and delivery of the Global Clinical Operations (GCO), clinical studies in accordance with the Operational Execution Plan (OEP) and clinical study protocol.
You will lead the cross-functional Clinical...
...mission to bring innovative medicines to patients worldwide. You will collaborate with colleagues from Statistics, Data Management and Clinical Development and have the opportunity to analyze data and derive key messaging to secure approvals from Health Authorities. Read on...