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...
...collected and in alignment with the protocol.
• Support the assessment of new data collection requirements in assigned studies and provide clinical input into the development of new and updated clinical Data Standards (for CRFs as well as 3rd party data collection methodologies)...
...lock with the oversight of the LCTL/CTL, as assigned. Support the clinical protocol development process in collaboration with the CTL/Lead... ...standards and operational procedures: attend CTT meetings, assist in report study progress and issues.
support the CTL/Lead CTL...
...knowledge of pharmacokinetics, pharmacodynamics, metabolism and clinical pharmacology in advancing the drug candidates from discovery and... ...of immunogenicity assay development and qualification, used to assisting with LBA method troubleshooting across a variety of platforms....
...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...
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...
...computer systems (including hardware and software) to program, write software, set up functions, enter data, or process information.
• Assists in the the acquisition and maintenance of property based systems.
• Assists in analyzing information, identifying current and...
...line with Hyatt International's Corporate Strategies and brand standards, whilst meeting employee, guest and owner expectations. The Assistant Manager - Digital is responsible to develop, implement, monitor and evaluate the hotel’s marketing communications strategy,...
Job Discretion:
Candidate should be graduate, preferable BE Electrical.
Candidate should have at least 1 year experience in same field.
Responsible for facilities deliverables.
Maintain a robust MIS and furnish details as and when necessary. MIS preparation and ...
Rs 1.8 - 2 lakhs p.a.
...suppliers.
Updating and maintaining procedural documentation.
JOB APPLY
CONTACT - RAKESH SINHA - (***) ***-****
ACCOUNTANT,ASSISTANT ACCOUNT,ACCOUNT OFFICER
Designation: ACCOUNT ASSISTANT/OFFICER - BOBBLI(AP)
Vacancies: 1
Experience: 1.0 Year(s) - 3.0 Year(s...
...accomplished construction professionals to enhance our team’s capabilities in Gujarat, Karnataka, Maharashtra, Telangana, and Andhra Pradesh. Assistant Manager Planning Qualification: BE - Civil with P.G/ Masters in Construction Management Industry: Construction Experience: 3-6 years...
Rs 1.4 - 2 lakhs p.a.
...Produce high end, superb cards using various machines, from collating to hot stamping.
JOB APPLY
SHASHI PRABHA - (***) ***-****
TAPPER,ASSISTANT
Designation: ASSISTANT/TAPPER (F-A & B ) - BPBBILI (AP)
Vacancies: 1
Experience: 1.0 Year(s) - 3.0 Year(s)...
Rs 4 - 5 lakhs p.a.
...JOB APPLY
SHASHI PRABHA - (***) ***-****
deputy manager electrical,electrical ferro alloys,deputy manager electrical ferro alloys
Designation: DEPUTY MANAGER/ASSISTANT MANAGER ELECTRICAL (FERRO ) - BOBBILI ( AP )
Vacancies: 1
Experience: 8.0 Year(s) - 12.0 Year(s)...
...new standards for customer service having operations across 300 locations in India.
For more details:
About the Role:
Assistant Operations Manager shall be responsible for the entire branch Operations and will manage all the operations colleagues directly (...
...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 to support compilation and release of submissions to...
...limited to:
• Provides scientific and medical expertise on assigned clinical projects. Contributes to clinical strategy for the Asian region.... ...and practice of Novartis SOPs and internal policies. Leads or assists with relevant trainings across TCO India
• Advocate continuous...
...improvements; Collaborate with Data Management team to enable reconciliation for locking of Clinical database. Alert the Medical Safety Physicians of potential safety issues and assist the Medical Safety Physicians in monitoring the safety profile of products.
• Member of...
...record finalization/action completion in the Third-Party Management, Clinical Trial Quality Risk Management, and Supplier Lifecycle Management... ...implementation, process management and training.
• Provide or assist with training of TM associates and provide support on related...
...product campaigns, new product launch campaigns as per Company s plans.
- Covers the Nursing homes, clinics and hospitals as per agreed coverage requirements.
- Assists in the collection of receivables, as per company policy.
- Work collectively with other team...
...and urgent nursing assessments effectively with our Healthcare clinical providers, including doctors, other nurses, and ancillary provider... ..., other injections, medications, and other treatments
- Assist all doctors with procedures as needed
- Patient education 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...
...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...
...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...
...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...
...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...
...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...
...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...