Apotex

Responsibilities: Assigning appropriate service provider depending on service requested and client’s needs. Prioritizing case assignment based on level of urgency. Relaying confidential client information to service providers within time sensitive standards. Communicating with service providers to relay updated client information and to request information needed to accurately service clients

Apotex Inc. founded in 1974, is the largest Canadian - owned pharmaceutical company. We employ over 6, 000 people worldwide in research, development, manufacturing and distribution. We produce more than 300 generic pharmaceuticals in approximately 4000 dosages and formats and export to over 115 countries around the globe. APOTEX RESEARCH PRIVATE LIMITED ARPL - based at Bangalore is engaged in

Founded in 1974 by Dr Barry Sherman, we’re a proudly Canadian, global pharmaceutical company that produces high-quality, affordable medicines for patients around the world.

About Apotex Inc. Job Summary: Executive - Pharmacokinetics responsible to implement CDISC standards in compliance with the regulatory requirement and managing all key activities of data management, software development and validations. Perform pharmacokinetics and statistical analysis of concentration - time data and to generate the randomization schemes, as and when required. Responsi

Job Requirements • Conducts duties following established Apotex Research Pvt. Ltd., Bioequivalence Centers Standard Operating Procedures and in a manner consistent with the appropriate regulatory guidelines, GCP requirements, and Safe Work Procedures. • Planning and coordinating the protocol training, Study Check-in activities with the study coordinator. • Request, and receive the Study Specific

Your Responsibilities Will Include Conferring with a physician to establish appropriate severity of illness and ensure documentation of principal diagnosis, comorbid conditions, complications, and procedures Perform concurrent/retrospective medical record reviews to monitor compliance Assist with clinical services Generate and assist with analysis of Reports Collaborate with Risk Management,

Responsibility Shall Include - listen to and Comprehend Patient Physician Interactions, Develop An Impression About the Clinical Condition and Document Plan of Action create and Summarize Findings and Insights Into Highly Structured Clinical Notes with Sections such as - History of Present Illness, Review of Systems, Physical Examination, Plan Details, Etc. populate the Summarized Data in

Job Description The candidates primary responsibility will be meeting doctors and promoting sales of various products of the company. The candidate will be required to achieve sales targets and ensure collections as decided and conveyed to the candidate by superiors and head office from time to time. The candidates concerted efforts should be aimed at improving overall efficiency and productiv

Prepare, conduct and report on activities related to the completion of site selection, initiation, routine monitoring and close-out visits Monitor patient enrolment to ensure recruitment targets and project timelines are met at the site and/or country level Perform source data verification and follow up on data queries at the site level, on-going review of any Risk Based Monitoring related inform

Primary Responsibilities Ensures clinical trial databases meet project requirements by: Reviewing documentation and requirements for new projects and anticipating impact to Data Management (DM) standards/processes Collaborating with appropriate project teams as needed to stay abreast of and changes that could affect data collection, cleaning and/or transfers Ensures the plan for data mana

Typical Responsibilities Include recording and reporting adverse reactions received from healthcare professionals and consumers conducting in-depth interviews with patients and healthcare professionals developing a thorough knowledge of products completing periodic safety update reports on drugs and other treatments writing and reviewing serious adverse effects reports and forms flagging up

Roles And Responsibilities In this role you are required to solve routine problems, largely through precedent and referral to general guidelines Your expected interactions are within your own team and direct supervisor You will be provided detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments The decisions that you make would impact

Responsibilities: Assist in the preparation of Core Lab Data Management documents; Perform validation on data transfers and edit programs; Maintain data cleanup via edits, data review and data changes; and Send data transfers externally.

Study scheduling and resource management (80%) Provides workload support in a scheduling function across multiple global services lines. Has knowledge in interpreting study designs and reviews design changes as they apply. Schedules milestones and details for studies run in the supported service lines. Updates and maintains proposal and schedule information in management information databases

Essential Job Duties ♦ Follow applicable departmental Standard Operating Procedures and Work Instructions. ♦ Complete required trainings according to timelines. ♦ Review and action queries on an ongoing basis and update database appropriately in accordance with Global Data Management Plans and applicable standardized data management. ♦ Perform UAT according to Validation Plan for

Job Responsibilities • Preparation of Process validation protocol, Cleaning validation protocol and cleaning evaluation report, trending and establishment of LCL and UCL, APQRs and VMP supporting documents. • Preparation of Trending reports (Raw materials, Intermediates and Finished API) as per the schedule. • Re-evaluations, Temperature Mapping, Equipment change controls, DM water Validation, E

The CDP-II shall be responsible for designing, programming, testing and maintenance of clinical trial databases in different clinical trial applications in accordance with standards. Perform external data loads, i.e. labs, ECGs etc., as needed. Act as liaison with vendors to establish data transfer specifications standards. Ensure all programming activities and processes performed are conducted

Clinical Trial Execution Assist in the management of study budgets including the set up of purchase orders and e-requisitions Order, track, and ship study supplies, tools, and/or instruments Track and report Regional/Global enrollment data for ongoing clinical studies Perform routine study activities per policies/procedures (e.g. Study closeout) Participate in shared learning forums May assis

Responsibilities: Perform quality assurance checks on echocardiographic imaging data to ensure protocol specific requirements are met; Perform established image processing techniques (converting imaging formats, performing preliminary cardiac measurements and volumes) on ECHO images using proprietary software as well as other third party software; Compile and maintain project-specific status r

Job Scope and Guidelines: Applies knowledge/skills to activities that often vary from day to day. Demonstrates a moderate level of knowledge and skills in own function. Requires little assistance with standard and non-standard requests. Solves routine problems on own. Works with supervisor to solve more complex problems. Prioritizes and organizes own work to meet agreed upon deadlines. Wor

Serves as a member of the project team with primary responsibilities for all documentation, requirements to support global EDC solutions tasks. Supports validation activities as assigned and serves as a validation team member. Writes and assembles validation documentation packages such as but not limited to, validation plan, test scripts, testing results, traceability matrix, validation reports.

To lead and participate in the development and maintenance of Signant Health’s global clinical data standards, including CRF CDISC Study Data Tabulation Model (SDTM), controlled terminology, and other applicable industry and customer standards Participate in relevant team meetings as SME for standards and provide input for data standards to customers and internal stakeholders (Business Development

Essential Job Duties Document and track study activities using relevant forms and tools, as well as relevant Project Management Systems with guidance/support Assist in the preparation of study and site specific materials in accordance with relevant SOPs Complete minute taking and documentation for sponsor/external or internal teleconferences as requested Assist in setting up and maintaining tra

Etiquette, Empathy, listening skills and good bedside manners Disease and applicable Pharma knowledge Good written and verbal communication including reporting accuracy Adherence to time schedules and processes including safety procedures Must have the ability to learn and retain complex material, pass tests demonstrating product and disease-related knowledge and deliver content to Customers ve

Role & Responsibilities: Excellent people friendly skills and ability to attract candidates to the organization. Excellent communication skills to interact with prospective and existing clients to describe hospital assignment details, pay, per diem and benefits. Create a high-quality pipeline of candidates by various outreach efforts, including via emails, high volume of calls, LinkedIn, FB, j

Job Requirements • Conducts duties following established Apotex Research Pvt. Ltd., Bioequivalence Centers Standard Operating Procedures and in a manner consistent with the appropriate regulatory guidelines, GCP requirements, and Safe Work Procedures. • Planning and coordinating the protocol training, Study Check-in activities with the study coordinator. • Request, and receive the Study Specific

Job Responsibilities • To execute the sampling and analysis of water samples, perform the Environmental monitoring and testing, swab sampling and testing, compressed air/Nitrogen gas monitoring • Perform the Microbial limit test of API, excipients, Intermediates and Finished goods. • Operate the autoclave for sterilization and decontamination. • Gram staining of organisms to identify the recove

Job Responsibilities • Documentation control: Issuance, Archival, retrieval and updating of documentation as per regulatory compliance • Publishing Documents in Apoweb , other links & sharefolders • Documents obsoletion. • Planning and co-ordination for reserve sample management activity. • Loading of Finished product, Raw Material and primary packaging reserve samples. • Annual Visual inspec

Job Responsibilities • Execute Corporate and supplier audits such as first GMP, routine, Targeted Technical Assessment (TTA) and For-Cause audits in accordance with Apotex's SOPs and current GMP regulations • Adopt the best practices of Excellence in Partnership to develop and sustain effective relationships with Apotex sites, suppliers, contractors, and business partners • Perform Due Diligence