job summary: Responsible for performing the accurate and detailed medical review of complex advertising and promotional materials and non-promotional materials. Provides timely and accurate reviews of promotional materials in accordance with established policies and practice standards, including regulatory guidelines to meet customer needs. Ensures deliverables convey a clear and appropriate medical message. location: Telecommute job type: Contract s
job summary: Responsible for performing the accurate and detailed medical review of complex advertising and promotional materials and non-promotional materials. Provides timely and accurate reviews of promotional materials in accordance with established policies and practice standards, including regulatory guidelines to meet customer needs. Ensures deliverables convey a clear and appropriate medical message. location: Telecommute job type: Contract s
job summary: The Medical Editor, Value & Access, is responsible for reviewing, editing, and supporting documents developed by Value & Access including AMCP dossiers, compendia, and product monographs. This individual provides editorial expertise for multiple projects across therapeutic areas within established timelines, interfaces regularly with medical writers to ensure accurate and timely delivery of information and contributes to cross-functional meet
job summary: The Medical Editor, Value & Access, is responsible for reviewing, editing, and supporting documents developed by Value & Access including AMCP dossiers, compendia, and product monographs. This individual provides editorial expertise for multiple projects across therapeutic areas within established timelines, interfaces regularly with medical writers to ensure accurate and timely delivery of information and contributes to cross-functional meet
job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that
job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that
job summary: Role is responsible for designing, planning, and executing large scale data analysis, and algorithm development to identify gaps in the care continuum and to measure impact using RWD. This work highlights the value of utilizing real world data to inform or address strategic questions in the disease areas of interest. The role involves the application of statistical theories, analytical methods, and technical programming skills to analyze clin
job summary: Role is responsible for designing, planning, and executing large scale data analysis, and algorithm development to identify gaps in the care continuum and to measure impact using RWD. This work highlights the value of utilizing real world data to inform or address strategic questions in the disease areas of interest. The role involves the application of statistical theories, analytical methods, and technical programming skills to analyze clin
job summary: Role is responsible for designing, planning, and executing large scale data analysis, and algorithm development to identify gaps in the care continuum and to measure impact using RWD. This work highlights the value of utilizing real world data to inform or address strategic questions in the disease areas of interest. The role involves the application of statistical theories, analytical methods, and technical programming skills to analyze clin
job summary: Role is responsible for designing, planning, and executing large scale data analysis, and algorithm development to identify gaps in the care continuum and to measure impact using RWD. This work highlights the value of utilizing real world data to inform or address strategic questions in the disease areas of interest. The role involves the application of statistical theories, analytical methods, and technical programming skills to analyze clin
job summary: Ensures accurate and consistent coding of medical data, including but not limited to, adverse event verbatim descriptions and medication data received from global clinical trials across all clinical areas including identification of prohibited medications and exclusionary medical history. Participates in Centralized Clinical Coding Group (CCCG) process improvement initiatives and serves as a subject matter expert and primary coding resource f
job summary: Ensures accurate and consistent coding of medical data, including but not limited to, adverse event verbatim descriptions and medication data received from global clinical trials across all clinical areas including identification of prohibited medications and exclusionary medical history. Participates in Centralized Clinical Coding Group (CCCG) process improvement initiatives and serves as a subject matter expert and primary coding resource f
job summary: A precision medicine company using innovative science to improve patient care and solve serious and costly problems. We are working to narrow the gap between scientific innovation and clinical decision- If you're passionate about having an impact on medicine, we'd love to hear from you. location: Telecommute job type: Permanent salary: $130,000 - 140,000 per year work hours: 9 to 5 education: Bachelors responsibilities: This
job summary: A precision medicine company using innovative science to improve patient care and solve serious and costly problems. We are working to narrow the gap between scientific innovation and clinical decision- If you're passionate about having an impact on medicine, we'd love to hear from you. location: Telecommute job type: Permanent salary: $130,000 - 140,000 per year work hours: 9 to 5 education: Bachelors responsibilities: This
job summary: As a Real-World Data (RWD) Scientist , you will be part of a team powering data driven insights that lead to better, faster decisions and therapies for our patients. Acting as a lead data scientist in your project area, you will contribute RWD expertise to broader cross-functional initiatives. Candidates should be excited to drive innovation by implementing new business technology solutions that solve significant scientific or business proble
job summary: As a Real-World Data (RWD) Scientist , you will be part of a team powering data driven insights that lead to better, faster decisions and therapies for our patients. Acting as a lead data scientist in your project area, you will contribute RWD expertise to broader cross-functional initiatives. Candidates should be excited to drive innovation by implementing new business technology solutions that solve significant scientific or business proble
job summary: We are seeking a skilled Validation Engineer to lead validation efforts for a new drug delivery site. This role involves protocol development and execution, audit support, validation assessments, and analyst training, all under limited to no supervision. The ideal candidate will have a strong background in GMP compliance, regulatory standards, and validation processes within the pharmaceutical or medical device industry. Schedule/Shift: 1st
job summary: We are seeking a skilled Validation Engineer to lead validation efforts for a new drug delivery site. This role involves protocol development and execution, audit support, validation assessments, and analyst training, all under limited to no supervision. The ideal candidate will have a strong background in GMP compliance, regulatory standards, and validation processes within the pharmaceutical or medical device industry. Schedule/Shift: 1st
job summary: The Biologics Drug Product Development team develops antibody drug conjugates (ADC) and other biologics by state-of-the-art formulation and analytical technologies. We create valuable intellectual property through new formulation compositions, cost effective manufacturing processes and prepare and defend CMC (Chemistry, Manufacturing and Control) regulatory content. We are looking for a highly motivated person to support Developability and Fo
job summary: The Biologics Drug Product Development team develops antibody drug conjugates (ADC) and other biologics by state-of-the-art formulation and analytical technologies. We create valuable intellectual property through new formulation compositions, cost effective manufacturing processes and prepare and defend CMC (Chemistry, Manufacturing and Control) regulatory content. We are looking for a highly motivated person to support Developability and Fo
job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that
job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that
A Global Biotech/Pharma located in Round Lake, IL is seeking a Manufacturing Technician to join their Team! Support manufacturing operations in Inspection and/or Packaging Inspect manufactured product for irregularities or defects Supplies components, small parts, glassware, tubing, etc. to cell culture and purification areas Operate general production equipment (such as labelers, parts washers, autoclave, stir plates, etc.) Complete relevant paperwork fo
A Global Biotech/Pharma located in Round Lake, IL is seeking a Manufacturing Technician to join their Team! Support manufacturing operations in Inspection and/or Packaging Inspect manufactured product for irregularities or defects Supplies components, small parts, glassware, tubing, etc. to cell culture and purification areas Operate general production equipment (such as labelers, parts washers, autoclave, stir plates, etc.) Complete relevant paperwork fo
The Manufacturing Technician I is responsible for executing processes in production at Takeda’s manufacturing facility in Round Lake, Illinois, while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations that apply. The incumbent will fully participate in both departmental projects and any quality working teams which may be applicable. Responsibilities include hands-on execution of all activities in t
The Manufacturing Technician I is responsible for executing processes in production at Takeda’s manufacturing facility in Round Lake, Illinois, while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations that apply. The incumbent will fully participate in both departmental projects and any quality working teams which may be applicable. Responsibilities include hands-on execution of all activities in t
The Manufacturing Technician I is responsible for executing processes in production at Takeda’s manufacturing facility in Round Lake, Illinois, while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations that apply. The incumbent will fully participate in both departmental projects and any quality working teams which may be applicable. Responsibilities include hands-on execution of all activities in t
The Manufacturing Technician I is responsible for executing processes in production at Takeda’s manufacturing facility in Round Lake, Illinois, while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations that apply. The incumbent will fully participate in both departmental projects and any quality working teams which may be applicable. Responsibilities include hands-on execution of all activities in t
job summary: Immediate opportunity for a Sr. Regulatory Affairs Associate, CMC to assist the technical team in preparing regulatory filing dossiers, assess changes for regulatory impact, and manage documentation systems. You will participate in Global Regulatory Product Team (GRPT) and Operations Brand Team meetings as needed. As a Senior Associate, RA CMC, you will work with internal and external partners in order to deliver products to patients. Prepare
job summary: Immediate opportunity for a Sr. Regulatory Affairs Associate, CMC to assist the technical team in preparing regulatory filing dossiers, assess changes for regulatory impact, and manage documentation systems. You will participate in Global Regulatory Product Team (GRPT) and Operations Brand Team meetings as needed. As a Senior Associate, RA CMC, you will work with internal and external partners in order to deliver products to patients. Prepare
A Global Biotech/Pharma located in Round Lake, IL is seeking a Manufacturing Technician to join their Team! Support manufacturing operations in Inspection and/or Packaging Inspect manufactured product for irregularities or defects Supplies components, small parts, glassware, tubing, etc. to cell culture and purification areas Operate general production equipment (such as labelers, parts washers, autoclave, stir plates, etc.) Complete relevant paperwork fo
A Global Biotech/Pharma located in Round Lake, IL is seeking a Manufacturing Technician to join their Team! Support manufacturing operations in Inspection and/or Packaging Inspect manufactured product for irregularities or defects Supplies components, small parts, glassware, tubing, etc. to cell culture and purification areas Operate general production equipment (such as labelers, parts washers, autoclave, stir plates, etc.) Complete relevant paperwork fo
