Labcorp

Labcorp Drug Development Hiring for safety science coordinator. Candidate should have excellent communication, working knowledge of the argus database.

Responsibilities • Facilitate the creation, revision or inactivation of all project training requirements in the LMS project training • Provide regular updates to project leaders and project coordinators on the status of all project related training requirements project training • Monitoring and tracking compliance of study teams to training requirements leveraging LMS repo

M&A Associate includes performing market analyses, data analyst  drawing up financial models, data analyst  (LBO, Business-Plans, Financing) and information memorandums, data analyst, drafting assessments and giving pitches. With data analyst dedicated financial skills and a sound feel for commerce, your interest in data analyst business makes the difference.

Responsible for collection of delinquent accounts, employing appropriate follow-up methods until payment has been received to resolve outstanding amounts with the goal of reduced DSO and improved past due A/R aging. Prepare reporting to describe the complete account status of significant collection issues.team lead • Review and analyze the aging for items as unapplied cash, short pay, and open

Mentor new recruits to ensure timely and accurate ICSR processing. Assist with the processing of case (Spontaneous, literature and clinical) as required in compliance with applicable regulations and Quanticate SOPs, pharmacovigilance and as requested by the Pharmacovigilance Scientist or above. Prepare case narratives as appropriate pharmacovigilance. Triage of cases for completeness, acc

Interviewing industry participants and related medical professionals Overseeing online and in-person physician surveys Searching Clarivate's proprietary in-house research repository/library for relevant data Using financial, regulatory, and government documents to find key medical approval data Model and forecast medical, data analystpharmaceutical, and healthcare markets data analyst , includ

Provides high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients.medical writer job  Demonstrates subject matter and therapeutic area expertise. May assist program managermedical writer job . Collaborates with internal and external clients, supporting and enabling effective and efficient communication tha

Performing monitoring visits according to plan, document actions and follow up on action plans Site feasibility visits incl. analysis of site logistics, clinical research site personnel performance/quality indicators and accountability for patient recruitment strategies Train and guide site staff in the protocol and trial procedures to minimize protocol deviations(PDs) Train site staff in safe

Role 1: Sr Medical Coders - Surgery || Noida upto INR 45k pm 1 Year Bond Role 3 : medical coder Medical Coding Trainee - Noida Life Science Graduate Fresher / Certified Medical Coders 2 Years Bond Required Candidate profile medical coder Aspirant must be a Certified Medical Coder Must have experience in relevant Specialization i.e. Surgery, ENM Fresher Science Graduate eligible for Traine

Experience in working with a Clearing House for submitting and receiving medical claims using EDI formatted files medical billing. o Experience with claim generation and claim posting processes medical billing. o Strong Knowledge of OOD/OOP software design patterns and principles medical billing. o Strong Knowledge of Core Java and Java open-source software components. medical billing o Experi

Productivity & Efficiency Coding related activities: Perform coding activities using medical dictionaries.medical coder Perform high level classification for coded terms. Data review related activities: medical coder Perform Serious Adverse Event Reconciliation. medical coderPerform medical review of all relevant data Design/ provide inputs to CRF and CRF Completion Guidelines. Create/ pro

The Lead Clinical SAS Programmer designs, develops, evaluates and modifies computer programs to analyze and evaluate clinical data, recognizes inconsistencies and initiates resolution of data problems. sas The Clinical Programmer typically creates programs using SAS to support the clinical research projects. RESPONSIBILITIES : - Collaborate with statistician and other functions to plan clinica

Position Overview: We are looking for a skilled UI Software Engineer with a strong background in Angular development to design, implement and support captivating user interfaces for our web applications. As a UI Software Engineer, you will play a crucial role in shaping the user experience of our products and ensuring they are both visually appealing and highly functional. The ideal candidate will

Essential Job Duties: • Support or manages all aspects of post-win through project closeout process (quote, budget) for opportunities as assigned • Responsible for managing some transactional clients • Review and analyze internal client documents to ensure adequate information for budget management is provided. Follow up with appropriate contact for additional information as required

These statements are intended to describe the general nature of the job and are not intended to be an exhaustive list of all responsibilities, skills, and duties.Obtains raw data from operational staff and conducts timely data back entry of study-related data into the data acquisition database. (20%)Conducts timely and accurate quality control for study-related data. (50%) .Learns to draft data tab

- Review clinical trial data in accordance with [Global] Data Management Plans and applicable standardized data management processes (SOPs; Work Instructions, etc.) to identify erroneous, missing, incomplete, or implausible data. - Run ancillary programs (e.g., diagnostics, special listings, reconciliation discrepancy listings) used to support the review of clinical trial data. - Generate, resolve

As a Clinical Project Associate at Labcorp, you will play a vital role in Lab Operations. Your responsibilities will include: • Follow Applicable SOPs and Work Instructions: • Adhere to departmental Standard Operating Procedures and Work Instructions. • Complete Required Trainings: • Ensure timely completion of required trainings. • Manage Day-to-Day Tasks: • Oversee day-to-day tasks ensuring

Job Description: Job Responsibilities: Review software requirements, create test plan, and test cases. Execute test plans, scenarios, scripts or procedures. Perform integration and user acceptance test cases Setup and run manual and automated tests Develop testing programs that address areas such as database impacts, software scenarios, or usability Document software defects, usin

Join us as we speed the delivery of groundbreaking therapies and anticipate tomorrow's drug development challenges, creating new possibilities for our clients--and your career. Labcorp's work in developing new pharmaceutical solutions has an incredible impact on the lives of millions worldwide. Be a part of this life-saving work. We have a great REMOTE opportunity to join our Metabolism team as

Assist with review of clinical trial data in accordance with Data Management Plans and/or Data Review Guidelines and raise queries to resolve erroneous, missing, incomplete data. Demonstrates capability to read and follow study timelines for on-time deliverables and potential to assist with inputs on study design or capable to make suggestions to study timelines when warranted. Run and execute addi

Labcorp is proud to be an Equal Opportunity Employer: As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (inclu

Labcorp Hiring Junior Regulatory affairs Specialist - Pune Department - ClinicalLocation: PuneJob type : full Time

Your new employer is Labcorp Drug Development, the world's most comprehensive drug development company, dedicated to improving health and improving lives. Our unique perspectives, built from decades of scientific expertise and precision delivery of the largest volume of drug development data in the world, along with our innovative technology solutions, help our clients identify new approaches and a

With unparalleled diagnostics and drug development capabilities, we accelerate innovation and provide insight to improve health and improve lives. Whether you’re a patient, provider, researcher or in the pharmaceutical industry, we’re here for you. With more than 70,000 employees strong, we serve clients in more than 100 countries. Labcorp (NYSE: LH) reported revenue of $14 billion in FY 2020.

• Implement consistent, efficient and quality processes to meet timelines and deliverables according to requirements and standard operating procedures • Ensure compliance of operations with governing regulatory requirements • Create, maintain and assume accountability for a culture of high customer service Operational • Execute drug safety data management processes xe2x80x93 a combination of cal

he Clinical Research Associate II (CRA II) is responsible and accountable for site monitoring and site management. Has responsibility for clinical studies according to Company, and/or Sponsor Standard Operating Procedures, and local regulatory guidelines. Assures the implementation of project plans, as assigned. Act in the project role of a Local Project Coordinator or Lead CRA as assigned. Esse

A LabCorp Pharmacovigilance job for freshers typically involves supporting the safety surveillance and risk management of drugs and medical products. The role may involve tasks such as collecting, reviewing, and tracking adverse event reports, conducting literature searches and reviewing scientific data, and preparing safety reports for internal and external stakeholders. Additionally, the Pharmaco

Sr. Clin Data Coord. #lifesciencegraduate #nagpurjobs #apportunities #clinicalresearchinstitute #smo #clinicalresearchcareers #clinicalresearchtrials #medicalresearch #healthcare #biology #pharmacovigilance #clinicalresearchtraining #education #bpharma #research #clinicalresearchers #nurse #clinicalresearchjobs #crc #pharmaceuticals #pharma #clinicaltrialsguru #clinicaldatamanagement #cralife #

Sr. Clinical Research Associate #lifesciencegraduate #nagpurjobs #apportunities #clinicalresearchinstitute #smo #clinicalresearchcareers #clinicalresearchtrials #medicalresearch #healthcare #biology #pharmacovigilance #clinicalresearchtraining #education #bpharma #research #clinicalresearchers #nurse #clinicalresearchjobs #crc #pharmaceuticals #pharma #clinicaltrialsguru #clinicaldatamanagement

Medical Reviewer #medicalcoding #medicalbilling #healthcare #doctors #medical #coding #icd #medicalcoder #aapc #physicians #physician #practicemanagement #medicalbillingandcoding #credentialing #revenuecyclemanagement #hospitals #cpc #telemedicine #physicaltherapy #medicare #medicaid #billingexperts #ehr #armanagement #nurses #grouppractices #hospitalmanagement #urology #medicalbillingandco

Medical Writer Asst #medicalcoding #medicalbilling #healthcare #doctors #medical #coding #icd #medicalcoder #aapc #physicians #physician #practicemanagement #medicalbillingandcoding #credentialing #revenuecyclemanagement #hospitals #cpc #telemedicine #physicaltherapy #medicare #medicaid #billingexperts #ehr #armanagement #nurses #grouppractices #hospitalmanagement #urology #medicalbillingandcol

Medical Writer II #medicalcoding #medicalbilling #healthcare #doctors #medical #coding #icd #medicalcoder #aapc #physicians #physician #practicemanagement #medicalbillingandcoding #credentialing #revenuecyclemanagement #hospitals #cpc #telemedicine #physicaltherapy #medicare #medicaid #billingexperts #ehr #armanagement #nurses #grouppractices #hospitalmanagement #urology #medicalbillingandcolle

Quality and Compliance Coordinator #regulatoryaffairs #ceos #pharmaindustry #qualitycontrol #humanerror #medicaldevice #cgmp #ceoinsights #healthcaree #pharma #hemptodaynews #hemp #carpetarea #cbd #hemptoday #brownfieldproject #water #compliancesolutions #hemprevolution #technology #lockdown #medtech #wastewater #lagos #laswarco #lagosstate #lagosstatecommission #itesiwajueko #regulatorycomplia

Safety Science Coordinator - 1 #regulatoryaffairs #ceos #pharmaindustry #qualitycontrol #humanerror #medicaldevice #cgmp #ceoinsights #healthcaree #pharma #hemptodaynews #hemp #carpetarea #cbd #hemptoday #brownfieldproject #water #compliancesolutions #hemprevolution #technology #lockdown #medtech #wastewater #lagos #laswarco #lagosstate #lagosstatecommission #itesiwajueko #regulatorycompliance

Document Coordinator #datasciencetraining #dataviz #tableau #excel #programmer #coder #datascientists #analyst #machinelearningalgorithms #powerbi #digitalmarketing #datascienceeducation #datastructure #ml #dataentry #dataengineer #analysis #career #code #pythoncode #datadriven #financialanalyst #developer #datacenter #businessanalysis #java #training #artificialintelligenceai #datasciences #so

Clinical Database Coordinator #clinicalresearch #clinicaltrials #clinicaldataanalyst #REGULATORYaffairs #medicalcoding #medicalbilling #research #healthcare #medicalresearch #clinicaltrial #science #clinical #health #clinicalstudies #pharma #medical #pharmacy #biotech #clinicareers #pharmacovigilance #pharmaceuticals #clinicalstudy #pharmacovigilance #medicalaffairs #clinicalresearchassocia

Central Monitoring Manager #clinicalresearch #clinicaltrials #clinicaldataanalyst #REGULATORYaffairs #medicalcoding #medicalbilling #research #healthcare #medicalresearch #clinicaltrial #science #clinical #health #clinicalstudies #pharma #medical #pharmacy #biotech #clinicareers #pharmacovigilance #pharmaceuticals #clinicalstudy #pharmacovigilance #medicalaffairs #clinicalresearchassociate #pha

LabCorp's Central Lab Data Manager is responsible for managing the flow of laboratory data and ensuring the accuracy and completeness of the data. The role may involve tasks such as overseeing data entry operations, verifying data accuracy, troubleshooting technical issues, and managing team members. Additionally, the Central Lab Data Manager may be responsible for developing and implementing data

LabCorp's Clinical Project Coordinator is responsible for supporting the coordination and management of clinical trials and research projects. The role may involve tasks such as communicating with study participants, scheduling appointments, managing study documentation, and tracking project progress. Additionally, the Clinical Project Coordinator may be responsible for coordinating the flow of inf

Statistical Programmer (3 -8 years) #statistical #inferentialstatistics #statisticians #statistics #stat #probability #statisticsandprobability #statslove #statlove #mathematics #inferential #statistic #statsforlife #biostatisticians #statsforlifee #estimation #significance #inference #nonparametric #parametric #datascience #bigdata #analytics #interpretation #testing Develop SAS programs for

This role may involve tasks such as reviewing study protocols and case report forms, verifying data accuracy, conducting database reconciliation, and generating study reports. Additionally, the Associate Clinical Data Analyst may be responsible for ensuring data quality, preparing data for statistical analysis, and working with the study team to resolve data-related issues. Ensure that all Data Ma

Responsible for supporting the creation of high-quality, scientifically accurate medical and scientific documents. The role may involve tasks such as writing and editing study protocols, informed consent forms, clinical study reports, and other study-related documents. Additionally, the Junior Medical Writer may be responsible for reviewing and summarizing scientific literature, assisting with the

Responsible for ensuring the quality and functionality of software products. The role may involve tasks such as writing and executing test cases, identifying and reporting software bugs, and conducting root cause analysis. Additionally, the Software Test Engineer may be responsible for developing and maintaining test automation scripts, working with software developers to resolve issues, and partic

Responsible for creating high-quality, scientifically accurate medical and scientific documents. The role may involve tasks such as writing and editing study protocols, informed consent forms, clinical study reports, and other study-related documents. Additionally, the Medical Writer II may be responsible for reviewing and summarizing scientific literature, assisting with the development of study-

Responsible for developing, testing, and maintaining statistical software applications and systems. The role may involve tasks such as writing code to perform statistical analyses, creating data visualizations, and automating complex processes. Additionally, the Statistical Programming may be responsible for working with statistical and clinical experts to understand their needs, writing and mainta

Responsible for supporting the collection, management, and analysis of clinical trial data. The role may involve tasks such as reviewing study protocols and case report forms, verifying data accuracy, conducting database reconciliation, and generating study reports. Additionally, the Clinical Data Associate may be responsible for ensuring data quality, preparing data for statistical analysis, and w

Responsible for analyzing and interpreting safety data related to medical products. This may involve tasks such as reviewing adverse event reports, conducting data analysis to identify safety trends, and presenting findings to stakeholders. Additionally, the Junior Safety Data Analyst may be responsible for ensuring data quality, preparing data for statistical analysis, and working with cross-funct

Serve as a central point of contact for employees and leaders for HR related inquiries via Service now System and phone line. • Provide superior customer service when responding to employee questions regarding payroll, company policies, benefits and general HR inquiries across the company. • Complete I-9 documentation and process using E-Verify system. • Facilitate off-boarding activities includ

1) 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 medical writer jobs 2) Ensure compliance of operations with governing regulatory requirements medical writer jobs 3) Create, maintain and assume accountability for a cultur

Qualifications  Bachelor's degree in Medical Science or equivalent degree  2-3 years of clinical practice experience preferred  Up to 2 years of pharmaceutical industry experience, medical manager including pharmacovigilance (case processing, medical review) and / clinical research preferred Special Skills & Knowledge medical manager  Clinical Research medical manager  Good

Ensure effective communication is occurring with LabCorp Drug Development Shared Service provider and LabCorp Drug Development collection group regarding cash application. • Monitor on Account cash application posting and duplicate payments to ensure that items are properly addressed on a timely basis. collection specialist  • Follow-up as needed to resolve outstanding amounts,