News & Vacancies
Perform medical writing tasks in collaboration with IO-SO and across regions.
Prepare protocols, clinical study reports, investigator’s brochure as per SOPs, timelines, guidelines and regulatory requirements.
Facilitate document-review meetings and provides comments-consolidated documents.
Co-ordinate the clinical document version reviews and approval processes. Ensure audit-preparedness.
Perform a literature search and prepare the summary of systematic literature search.
Critically analyses large numbers of articles from biomedical published literature and internal drug safety alerts and identifies individual case safety reports (ICSRs) as well as other potential safety-relevant information impacting the risk-benefit and/or safety profile of customer’s products, as per applicable regulatory requirements and standard operating procedures.
Develop high quality medical and scientific content
Should be fluent in written and spoken English and should have excellent communication skills
Should also be confortable in client and KOL interactions.
• Lead, support and report independent Good clinical practice (GCP) and Pharmacovigilance (PV) audits according to the Sandoz Quality System and the current GCP and PV regulations to assess compliance with applicable regulations, standards, and guidance documents. Review and approve corrective action plans in support of the audit observations. The audits performed include internal and external executors involved in pre-clinical and clinical studies and any step of Pharmacovigilance PV process.
Assist with electronic formatting of submissions of global regulatory filings, in accordance with agency guidance.
To maintain lists / documents / reports
Data entry in Orion internal system like Pallas, Enovia
Miscellaneous administrative activities as assigned
Assist with electronic formatting of submissions of global regulatory filings, in accordance with agency guidance.
To maintain lists / documents / reports
Data entry in Orion internal system like Pallas, Enovia
Miscellaneous administrative activities as assigned
Review and execute physician’s prescriptions checking their appropriateness and legality
Organize the pharmacy in an efficient manner to make the identification of products easier and faster
Maintain full control over delivering, stocking and labeling medicine and other products and monitor their condition to prevent expiring or deterioration
Listen carefully to customers to interpret their needs and issues and offer information and advice
Provide assistance other medical services such as injections, blood pressure/ temperature measurements etc.
Prepare medicine when appropriate using correct dosages and material for each individual patient
Keep records of patient history and of all activities regarding heavy medication
Keep abreast of advancements in medicine by attending conferences and seminars and collaborating with other healthcare professionals
1. Need to validate the approval request from the Registration department and send the approval request to the payer
2. Assist the patient/physician in getting approval for the procedure from Payers via email or phone calls.
3. Validate the CPT, and ICDs in HIS & request approval for the procedures or services in the payer portal or HIS
4. Co-ordinate with physician/ payer to get approval for the services as per the authorization protocol.
5. To ensure the Deductible, copay & coinsurance are updated in the HIS system as per the patient's insurance card.
Medical coding Trainer, Oncology - Radiation Oncology, Medical Oncology, and Surgical Oncology.
Job Role: Medical Coder
Qualification: B.Pharmacy/M.Pharmacy/D.Pharmacy
Skills Required: Strong Knowledge in Medical Coding
Salary: 1.8 LPA to 2.4 LPA
Location: Hyderabad (Work from Home till COVID)
Mandatory Requirements: Laptop & Internet Connection
Skills: medical coding
Role- Medical Coder: We are looking to hire an experienced Coder / Sr. Coder with active coding certifications (CPC / CPC-A / CIC / CCS / COC). With strong domain expertise in CPT and ICD (diagnosis) coding, the incumbent should be able to validate the coding after reviewing all relevant medical records ensuring codes are accurate and sequenced correctly in accordance with government and insurance regulations.
Working in an evolving healthcare setting, delivering innovative solutions using our shared expertise. Using opportunities to learn and grow through rewarding interactions, collaboration, and the freedom to explore professional interests.
Giving priority always to what is best for our clients, patients, and each other. With our proven and scalable operating model, complementing a healthcare organization’s infrastructure to quickly drive sustainable improvements to net patient revenue and cash flows while reducing operating costs and enhancing the patient experience.
• Provide support according to the needs for delivery activities, i.e. SUSAR ICSR medical review when needed, co-authoring safety documents and assisting in providing safety input to regulatory and clinical documents, as well as ad hoc Health Authority queries.
• Assist the GPSL/MSL in monitoring the safety profile of products including with activities such as literature review, medical assessment and related activities for single cases, including collecting additional follow-up information as necessary, medical evaluation of quality defects or signal detection. Medical review of single case reports will be performed by associates possessing medical degree.
• Perform Literature review for PSUR inclusion and assessment of literature for signals. Provide support for the preparation of ad hoc Health Authority queries, provide input into responses to inquiries from health care professionals on safety issues
• Together with the Safety Leads, co-author the PSUR sections as required, including analytical input to PSUR for identified and potential risks defined in the Risk Management Plan (RMP) and new safety signals. Perform follow up activities on Health Authority Assessment Reports.
• Assist in evaluating and writing other safety deliverables including but not limited to Clinical Overview, Development Safety Profiling Plan (d-SPP), and Development Safety Update Report (DSUR).
• Owns the safety strategy of the assigned products and ensures ongoing evaluation of the overall safety profile, serving as the medical safety representative for Risk Management Plans (RMPs), Periodic Safety Update Reports (PSURs), Annual Product Quality Reports (APQRs) and medical risk assessments (MRAs).
• Provide safety input (Addendum to Clinical Overview) for license renewal documents, Co-author medical assessment of product quality issues. Contribute to the development and update of RMPs in collaboration with MSL/GPSL, coordination with other functions
Track and maintain metrics regarding the status of the data within EDC systems
Clean the clinical database, which includes generating and resolving data clarifications
Reconcile clinical data
Assist with support activities for the Data Management department
Responsible for QC2 and review of study documentation for Trial Master File (TMF) quality for sponsor and/or CRO studies
• Perform study lead responsibilities, be responsible for the assigned studies, and ensure that the project runs smoothly from start to end
• Keep project mappings up-to-date, coordinate with Project Managers (PMs) to ensure required changes are made both in the mapping document and in Trial Interactive (TI)
• Communicate with PMs and the team to ensure the project timelines are met and a good quality TMF is maintained
• Work on cross functional teams including Project Management, Business Development, Client Services, Development, and IT on the implementation and management of client projects
Study / analysis of inventions to determine patentability, Conduct Invalidity and Freedom to
Operate searches,
• Prepare robust search strategies to search and identify relevant patent and scientific literature
in a given technology domain, and subsequent analysis,
• Analysis of a portfolio of patents / patent applications in a given technology domain,
• Critical analysis of patents and products to determine potential infringement and licensing
opportunities,
• Track / monitor published patent applications and issued patents throughout their life cycle,
• Identify key features of a product / technology and map these features on to patented subject
matter to determine freedom to operate,
• Prepare research reports to be shared with scientists / R&D Managers / technical personnel of
the client organization etc.
Skill required: Content Management - Medical Affairs
Designation: Marketing Senior Analyst
Job Location: Mumbai
Qualifications: MBBS/Master of Pharmacy/MD
Years of Experience: 5 to 6 years
Bachelor of Science in Pharmacy / Bachelor of Science in Nursing / PharmD / PhD or Masters in relevant field or Medical Degree (MBBS or MD) required. Medical degree with specialization preferred. Medical degree is essential for associates performing medical review of single case reports whenever business needs require this activity.
• For life sciences graduate - 3 years in patient safety at an operational or medical position. May be a first job in the pharmaceutical industry for an MD or with 2 or more years of clinical experience after MBBS.
• Experience in safety document or medical writing including experience coding with MedDRA and WHO dictionaries. Excellent understanding of clinical trial methodology, ICH GCP, GVP guidelines and medical terminology
• Attention to detail and quality focused. Strong organizational and project management skills. Strong communication skills, and the ability to operate effectively in an international environment
• Excellent understanding of Human physiology, pharmacology, clinical study objectives, and the drug development process. Strong technical understanding of Biomedical/Biostatics concepts and problem-solving skills
• Good presentation skills. Strong computer skills including, but not limited to, creation of spreadsheets, templates, presentations and working with safety databases/applications
• Ability to work independently, under strict timelines, demonstrating initiative and flexibility through effective innovative leadership ability
Delivering and managing multiple concurrent consulting projects addressing corporate sustainability frameworks, standards, strategy, stakeholder engagement and materiality assessment, reporting, data management etc.
Working with Excel (or other data formats) to manage comprehensive data and data structures
Performing analysis on energy, water, waste, and emissions
Preparing and presenting project results in PowerPoint or other formats,
Writing reports and documenting your project work,
Ensuring your projects adhere to scope, schedule, budget, and quality, and
Working together with Sphera team members across different specialties and regions.
Receive training on Functional Verification Methodologies at IP and SoC level using SystemVerilog and UVM
Be able to work on verifying designs using Synopsys Simulation tools
Develop Test-bench & Reference models in IP & SoC level verification environments
Document and Implement Verification Plans
Work closely with design engineers to create constrained random based test-benches and test cases to meet the required functional and code coverage metrics
Debug and help resolve test failures
Create reusable verification environments to be used across multiple teams
Complete internship project as per plan
We are looking for candidates with 3+ years of experience in core data management activities, if this sounds like your perfect job opportunity, don't hesitate! You can also share your updated CV to swathy.anandan@docsglobal.com
When and where:
Date: 2nd and 3rd June, 2023 from 9 AM IST.
Location: ICON plc, Block 1, 4th Floor, Prestige Blue Chip Software Park, Dairy Colony, Adugodi, Bengaluru, Karnataka 560029. Opposite Christ college.
Implement and promote use of consistent, efficient and quality processes to meet timelines and deliverables according to requirements and standard operating procedures, and assume accountability for the deliverables
Ensure compliance of operations with governing regulatory requirements
Create, maintain and assume accountability for a culture of high customer service
Efficiency in conducting literature searches for authoring various types of reports
Write and review various safety reports (or part of such reports) for global regulatory submissions for Labcorp’s clients, including Annual Reports (IND and other), Periodic Safety Update Reports, Periodic Adverse Drug Experience Reports, Periodic Benefit-Risk Evaluation Reports, Bridging reports and other clinical documents, as assigned.
Perform/review Signal detection activities
Author/ review RMPs, ad hoc reports, Safety Update reports, Benefit-Risk Evaluation, CCDS supporting document, ACOs, Addendum reports
To assist marketing and sales team in sharpening and positioning of product and promotional strategies. Foresee the challenges and changing market dynamics and make timely corrective and preventive actions.
You will stay updated on scientific knowledge by actively participating in scientific meetings, gather clinical insights/needs/feedback from key opinion leaders and communicate to internal stakeholders.
Responsible for educating and training the field and marketing personnel and other relevant stakeholders regarding all aspects of disease, product and therapy relevant to promotional strategy.
You will build a strong advocacy of Novo Nordisk’s portfolio with key external stakeholders through on-going/robust scientific interactions.
Conducting systematic/targeted/structured literature reviews
Developing and perform database searches and writing protocols for literature reviews
Identifying relevant evidence for research questions (primary and secondary screening)
Extracting, analysing, and summarising data from a range of sources Performing quality checks to ensure data accuracy
Summarising literature review findings in a report/slide-deck
Providing writing support for HTA submissions and publications based on HEOR studies
Communicating with the clients and the internal project team to ensure smooth and timely execution of the project.
Provide guidance, support, and mentorship to team members.
Monitor progress, identify potential issues, and implement necessary adjustments.
The Annual Report Submission Planner is responsible to provide regulatory filing support for assigned Annual Report by providing required submission activities (planning, obtaining required data (CMC/ancillary documents), coordination, reviewing, and release) in accordance to regulatory requirements and timelines.
Respond to health authority questions or local subsidiary requests for additional information to support the Annual Reports.
Administrative Content (Module 1) preparation for Annual Reports-US market.
To handle Regulatory document management systems: ORION -COGNOS, VEEVA, REDS, SPARS etc.
Coordination with clients in tracking and status update of project plans.
Ensure a timely submission of Annual Reports to the agency.
Coordination team review, electronic content publishing, and release of the Annual Report submission content.
Willing to work for US Shift
Position wanted:
R&D Formulator 1 and 2
Location: Riyadh, Saudi arabia.
Experience: 3-5 years
Background: semisoslid,solid and liquid dosage forms.
Candidate with experience in development of cosmetics and Medical disinfectant also apply.
Send your CV to :mohamed.eliyas@nationalpharma.com.sa
Salary and other perks as per industrial standard.
Fielding all incoming help requests from clients via telephoneand/or emails in a courteous manner
Document all pertinent end user identification information,including name, department, contact information and nature of problem orissue
Update own availability in the RAVE system to ensureproductivity of the process
Record, track, and document all queries received, problem-solving steps taken and total successful and unsuccessful resolutions
Follow standard processes and procedures to resolve all clientqueries
Resolve client queries as per the SLA’s defined in thecontract
Access and maintain internal knowledge bases, resources andfrequently asked questions to aid in and provide effective problemresolution to clients
Identify and learn appropriate product details to facilitatebetter client interaction and troubleshooting
Document and analyze call logs to spot most occurring trends toprevent future problems
Maintain and update self-help documents for customers to speedup resolution time
Identify red flags and escalate serious client issues to Teamleader in cases of untimely resolution
Ensure all product information and disclosures are given toclients before and after the call/email requests
Avoids legal challenges by complying with service agreements
Identify and approach dental hospitals in the city for onboarding the company's products and services
Build and maintain relationships with dental hospital decision-makers and key influencers
Communicate the features and benefits of products and services to dental hospital decision-makers and key influencers
Analyze market trends and identify opportunities for growth
Develop and implement sales strategies to achieve onboarding targets
Execute promotional plans to increase product awareness and sales
Provide product training to dental hospital decision-makers and key influencers.
• Collect and report market intelligence to the management team.
• Maintain accurate records of onboarding activities and customer interactions.
To research and develop an online drug database.
Review pharma contents as and when required by the organization.To maintain hygiene in the drug database through periodic monitoring and ensuring that the database is up to date and complying to all the rules and regulations in a timely manner.
Sound Knowledge and ability to apply the governing Acts like Drugs and Cosmetics Act, Narcotic Drugs and Psychotropic Substances Act, etc.,
Strong communication (written and verbal) and presentation skills.Strong problem solving, influencing, negotiation, conflict management and collaboration skills.
Good MS office and computer skills.Highly effective time management and delegation skills, ability to manage multiple competing priorities, meet multiple demanding timelines and work creatively in a fast-paced, target-driven high-pressure environment.
Ability to work in a team and to carry out assignments to completion within parameters of instructions given, prescribed routines and standard accepted practices.
Ability to deliver results to the appropriate productivity, budgetary and quality metrics.Demonstrated flexibility, initiative, proactivity, ownership and accountability.
The candidate must be managing Amazon platform completely.
He/she must be well versed with all aspects of Amazon advertisements related matter(e.g. Sponsored Products, Sponsored Brands, Sponsored Display)
Potential candidate must know RoI / PPC / daily , weekly , monthly budgets
He / she should be pro-active, must be able to deal with all stakeholders and ensure strict time-lines
The candidate must know online ad's/ campaigns / google ad's
Achieving desired Sale targets by using different types of advertising keeping ACOS in control.
Develop and execute Amazon advertising campaigns to increase sales and product visibility
Optimize ad campaigns by monitoring and analyzing performance metrics, adjusting targeting, and refining messaging to improve ROI
Conduct keyword research to identify relevant search terms and optimize product listings for increased discoverability
Manage the day-to-day sales operations of our Amazon store, including inventory management, pricing, and product listings
Monitor and optimize product performance through analysis of sales data, customer feedback, and competitor activity
Work closely with our customer service team to resolve any issues or complaints from Amazon customers
Conduct market and competitive research to identify opportunities and inform business decisions
Analyze and report on performance metrics, identifying trends and areas for improvement
Keep up-to-date with Amazon policies, trends, and best practices, and implement changes as needed to stay ahead of the competition
Excellent English language skills including reading, writing and speaking.
Ability to communicate fluently with foreign nationals.
Self-motivated, passionate and energetic professionals.
Minimum 6 months of Full Cycle Recruiting experience particularly in pharmaceutical / Pharma / Healthcare / Hospital / Nurse / life science domain for US staffing and recruiting industry .
Day-to-day, comprehensive monitoring of global industry, regulatory, financial, clinical and social media sites/feeds using a variety of secondary research resources
Extensive use of databases such as Globaldata, Inframation, Factiva, etc. and an understanding of how to extract information from government and client sites
Keen at researching on market trends, analyzing data from competitors, and analyzing the business's operations, expenditures, and performances to identify patterns of potential issues or improvements
Creating project appraisal tools to provide in-depth analysis of project pipeline to the sales leadership
Setting of alerts in many resources as well as on Google and company websites
Project team assignments that involve providing client profiles, client strategies, competitor analysis, etc
Collaborating with team members and helping with ad hoc research requests involving in-depth searches for information
Identify and approach dental hospitals in the city for onboarding the company's products and services.
Build and maintain relationships with dental hospital decision-makers and key influencers.
Communicate the features and benefits of products and services to dental hospital decision-makers and key influencers.
Analyze market trends and identify opportunities for growth.
Develop and implement sales strategies to achieve onboarding targets.
Execute promotional plans to increase product awareness and sales.
Provide product training to dental hospital decision-makers and key influencers.
Collect and report market intelligence to the management team.
Maintain accurate records of onboarding activities and customer interactions.
Medical Administrator is responsible for efficient functioning of clinical services and the quality of care. Oversees all the medical and paramedical activity in the Hospital.
Implements the management decisions and rules of the Hospital and supervises their implementation, Supervision of day-to-day administration, Ensures physical facility and equipment are adequately available, Ensures proper upkeep and confidentiality of records, Assist in the appointment of medical and paramedical staff., Ensure following of proper procedure for admission, care and discharge of patient, Coordinate with Consultant and Referral Doctors, Be the legal representative of the management, Ensures compliance with all the Govt. statutory regulation
Collecting, analyzing, and interpreting data on procurement categories and market trends
Deliver practical insights to support the development and execution of procurement category strategies
Develop and maintain procurement KPIs, scorecards, and reports to track performance and identify improvement opportunities
Manage and maintain procurement data reclassification efforts, ensuring accurate and up-to-date data
Develop and maintain procurement dashboards and visualizations to support decision-making and communication with collaborators
Conducting research on industry trends, suppliers, and products to support procurement strategies
Participating in procurement projects and initiatives, providing insights and recommendations to the team