Emcure Pharmaceuticals

Clinical Data Programmer provides technical expertise for the conduct of clinical trials and works independently to support various programming activities related to clinical data systems, and/or the applications within. Independent contributor role with proven ability work with virtual cross functional global teams.

Job Summary Perform processing for all types of safety events, medical information call handling activities and other medically-related project information. Ensure all , Sponsor, and regulatory timeframes are met for the processing and reporting of safety information Assist in ensuring the completion of all departmental project activities accurately in accordance with standards, regulatory re

Daily job tasks for SAS programmers differ based on the data they analyze and the statistical information they compile. Import and Export Raw Data SAS programmers import and export raw data to add information to and extract information from various databases. Manage Databases SAS programmers manage and maintain databases containing large quantities of information. This includes backing

Qualification : Diploma in Pharmacy/ Degree in Pharmacy/ D Pharma/ B Pharmacy Experience : 0 to 10 years Gender : M/F

Cold call and visit prospects on location , Set appointments with hospital staff and administration. Manage all leads, Build Relationship with Hospital and Doctor, Communicate between sales , marketing and support teams to improve customers Experience.

You Will Be Responsible For Implementing marketing strategies & campaigns for product promotion to doctors Performing effective in-clinic presentation to doctors Identifying and promoting right product for right doctors Doing retail chemist prescription audit Timely reporting and achieving value/volume target.

Assists in the tracking of planned and scheduled audits in the enterprise quality management system. Updates audit schedules and calendars as requested by management. Assists in gathering documentation required by auditors for audits and inspections (e.g. training records, organizational charts). Assists auditors in obtaining follow-up information during customer audits and regulatory inspection

Training skills are mandatory Responsible for conducting online and offline classes. Develop curriculum and create presentation Train, educate and develop employees and freshers on inpatient and outpatient coding skill sets and competencies based on the industry requirements. Review and respond to coding questions Research on updated coding issues, reimbursement methodologies, and changes in techno

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 i

Effectively collect and evaluate data, information, and input from multiple sources, functions, and regions to create a cohesive content strategy for writing projects. Plan (including organizing/preparing outlines), write (including first-draft authoring), edit, review, coordinate, and complete the regulatory documents supporting clinical development/product registration. Conduct effective docume

Review marketing materials against an established set of guidelines and brand standards, enter results into database, and communicate results of the review to advertisers. Conduct primary review of post campaign activities to determine whether advertisements were executed as specified in program guidelines. Complete administrative tasks such as filing, letter processing, mailing, etc. Perform we

Job Requirements • Maintain good Relationship with Doctors, Chemist, Stockist and meeting sales goals. • Maintaining proper Call Average • Meeting Doctors to promote the company range of products in the territory • Generate prescriptions from doctors by providing scientific information about the products and explaining the benefits gained by using them • Meeting retail chemists to make sure th

Preparation / authorisation of Master BPRs, artwork, component specifications, labels, reprocessing paperwork, pre-batch documentation, calibration records, temperature records, environmental reports, MWOs, etc. Liaison with customers on issues relating to quality matters, presenting quality related data and attending and presenting at quality review meetings. Assist with initiating any nonconfor

 Undertakes primary medical review of cases, including medical assessment of the case for seriousness, listedness/labeling, causality, adverse event coding and narrative review.  Updates and documents daily case data, case-feedback in appropriate trackers/tools to facilitate tracking and workflow management  Assumes complete responsibility for all assigned deliverables in line with e

Serve as an internal consultant and Veeva Vault expert for IT and business partners across regions and business areas. Participate in business requirement gathering and design activities with business & IT collaborators as part of scrum team. Perform delivery activities through Design / Build / Test / Deploy phases for regular releases and key Veeva platform initiatives. Design and build extensi

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 reports and project ti

Enters information into PVG quality and tracking systems for receipt and tracking ICSR. Processes ICSRs according to Standard Operating Procedures (SOPs) and project/program-specific safety plans. Triages ICSRs, evaluates ICSR data for completeness, accuracy, and regulatory report ability. Enters data into safety database. Codes events, medical history, concomitant medications and tests. Compi

The purpose of the role is two-fold: To ensure clinical study data is collected, transformed, and validated to industry and customer data standards, ensuring high-quality data is delivered to customers for statistical analysis, within agreed upon project timelines. To provide input to internal departments as the SME and to build and maintain global data standards

1. Candidate will be based at Mumbai office of Emcure Pharmaceuticals and will be handling Medico Marketing function of Gynae. 2. Candidates will be responsible to the organization/division by taking responsibility for the scientific, technical and ethical soundness of all policies, statements and endeavors. 3. He/She will be responsible for actively support development of promotion of alloca

Responsible for portfolio management of API business vertical w.t.r. new introduction, retirement, and sustenance. Coordinate monthly API portfolio meeting and work closely with key functions like BD, RD, IP , RA etc. Responsible to create product strategy within various geographies of market along with BD. Evaluate product competitiveness and business intelligence for our API portfolio. Recomm

Planning, prioritizing and tracking the meetings of the President basis the agenda and business priorities. Being part of all the meeting and preparing Minutes of Meeting and sharing with the listed participants. Creating Action Plan basis those meetings. Following up, tracking and updating the progress on the action plan. Working on the Data and Presentation based on requirement. Attending fe