Massachusetts Bay Transportation Authority (MBTA) At the MBTA, we envision a thriving region enabled by a best-in-class transit system. Our mission is to serve the public by providing safe, reliable, and accessible transportation. MBTA’s core values are built around safety, service, equity, and sustainability and each employee that works for the MBTA performs their roles based on our vision, mission, and values. This includes attendance, participation, and contribution in local safety committee meetings as needed. Job Summary The Civil Rights Compliance Investigator performs monitoring and oversight of the MBTA's Disadvantaged Business Enterprise (DBE) program requirements on USDOT-assisted construction projects. This position sits in the Office of Diversity and Civil Rights (ODCR), a shared office between MassDOT and the MBTA. The responsibilities of the Civil Rights Compliance Investigator include, but are not limited to, collaborating with the MBTA's Office of...

CareFirst BlueCross BlueShield Resp & Qualifications PURPOSE: The role of the Special Investigations Unit (SIU) Investigator, Sr. is to assist in the reduction and recuperation of losses to CareFirst through the detection, investigation, and resolution of all levels (low to complex), of fraud, waste, and abuse schemes, resulting in the savings and recovery of funds. ESSENTIAL FUNCTIONS: Independently or as lead in part of an assigned team develop and conduct healthcare fraud, waste, and abuse investigations of all levels (low to complex). Develop and execute investigative plans that may include performance of audits of financial business records, provider and subscriber medical data, claims, systems? reports, medical records, analysis of contract documents, provider/subscriber claims history, benefits, external data banks and other documents to determine the possible existence of fraud and/or abuse. Conducting detailed offsite audits/investigations with...

CareFirst BlueCross BlueShield Resp & Qualifications PURPOSE: The role of the Special Investigations Unit (SIU) Investigator, Sr. is to assist in the reduction and recuperation of losses to CareFirst through the detection, investigation, and resolution of all levels (low to complex), of fraud, waste, and abuse schemes, resulting in the savings and recovery of funds. ESSENTIAL FUNCTIONS: Independently or as lead in part of an assigned team develop and conduct healthcare fraud, waste, and abuse investigations of all levels (low to complex). Develop and execute investigative plans that may include performance of audits of financial business records, provider and subscriber medical data, claims, systems? reports, medical records, analysis of contract documents, provider/subscriber claims history, benefits, external data banks and other documents to determine the possible existence of fraud and/or abuse. Conducting detailed offsite audits/investigations with...

GSK GSK has an inspiring ambition: by uniting science, technology and talent we aim to positively impact the health of 2.5 billion people over the next ten years. We will get ahead of disease together with our R&D approach of focusing on the science of the immune system, human genetics and advanced technologies, such as functional genomics and AI/ML. Job Purpose: We have an exciting opportunity at GlaxoSmithKline (GSK) for a highly innovative Quantitative Clinical Pharmacologist to join our team supporting infectious disease area as part of the global department of Clinical Pharmacology Modelling & Simulation. GlaxoSmithKline provides a supportive environment for scientists who are aspiring to learn, to contribute and to make impact on business decisions through innovation, expertise, and influence. As a Director of Clinical Pharmacology Modelling and Simulation (CPMS) you will be part of a science driven group delivering clinical pharmacology and modelling &...

Truist The position is described below. If you want to apply, click the Apply Now button at the top or bottom of this page. After you click Apply Now and complete your application, you'll be invited to create a profile, which will let you see your application status and any communications. If you already have a profile with us, you can log in to check status. Need Help? If you have a disability and need assistance with the application, you can request a reasonable accommodation. Send an email to Accessibility (accommodation requests only; other inquiries won't receive a response). Regular or Temporary: Regular Language Fluency: English (Required) Work Shift: 1st shift (United States of America) Please review the following job description: This position will sit in-office 4 days a week, locations for consideration are listed. No remote option available. No additional locations will be considered. Provide internal and external preliminary...

Truist The position is described below. If you want to apply, click the Apply Now button at the top or bottom of this page. After you click Apply Now and complete your application, you'll be invited to create a profile, which will let you see your application status and any communications. If you already have a profile with us, you can log in to check status. Need Help? If you have a disability and need assistance with the application, you can request a reasonable accommodation. Send an email to Accessibility (accommodation requests only; other inquiries won't receive a response). Regular or Temporary: Regular Language Fluency: English (Required) Work Shift: 1st shift (United States of America) Please review the following job description: This position will sit in-office 4 days a week, locations for consideration are listed. No remote option available. No additional locations will be considered. Provide internal and external preliminary...

Truist The position is described below. If you want to apply, click the Apply Now button at the top or bottom of this page. After you click Apply Now and complete your application, you'll be invited to create a profile, which will let you see your application status and any communications. If you already have a profile with us, you can log in to check status. Need Help? If you have a disability and need assistance with the application, you can request a reasonable accommodation. Send an email to Accessibility (accommodation requests only; other inquiries won't receive a response). Regular or Temporary: Regular Language Fluency: English (Required) Work Shift: 1st shift (United States of America) Please review the following job description: This position will sit in-office 4 days a week, locations for consideration are listed. No remote option available. No additional locations will be considered. Provide internal and external preliminary...

Truist The position is described below. If you want to apply, click the Apply Now button at the top or bottom of this page. After you click Apply Now and complete your application, you'll be invited to create a profile, which will let you see your application status and any communications. If you already have a profile with us, you can log in to check status. Need Help? If you have a disability and need assistance with the application, you can request a reasonable accommodation. Send an email to Accessibility (accommodation requests only; other inquiries won't receive a response). Regular or Temporary: Regular Language Fluency: English (Required) Work Shift: 1st shift (United States of America) Please review the following job description: This position will sit in-office 4 days a week, locations for consideration are listed. No remote option available. No additional locations will be considered. Provide internal and external preliminary...

Truist The position is described below. If you want to apply, click the Apply Now button at the top or bottom of this page. After you click Apply Now and complete your application, you'll be invited to create a profile, which will let you see your application status and any communications. If you already have a profile with us, you can log in to check status. Need Help? If you have a disability and need assistance with the application, you can request a reasonable accommodation. Send an email to Accessibility (accommodation requests only; other inquiries won't receive a response). Regular or Temporary: Regular Language Fluency: English (Required) Work Shift: 1st shift (United States of America) Please review the following job description: This position will sit in-office 4 days a week, locations for consideration are listed. No remote option available. No additional locations will be considered. Provide internal and external preliminary...

Truist The position is described below. If you want to apply, click the Apply Now button at the top or bottom of this page. After you click Apply Now and complete your application, you'll be invited to create a profile, which will let you see your application status and any communications. If you already have a profile with us, you can log in to check status. Need Help? If you have a disability and need assistance with the application, you can request a reasonable accommodation. Send an email to Accessibility (accommodation requests only; other inquiries won't receive a response). Regular or Temporary: Regular Language Fluency: English (Required) Work Shift: 1st shift (United States of America) Please review the following job description: This position will sit in-office 4 days a week, locations for consideration are listed. No remote option available. No additional locations will be considered. Provide internal and external preliminary...

CSL The Opportunity The CQA Manager is a global role managing Global CQA activities in the respective regions (Asia-Pacific, Americas, EMEA, Japan) and globally. Under guidance of the Head CQA Operations in the respective region, you will be responsible for planning, maintenance, and implementation of the assigned Global R&D Quality Audit Program with focus on Clinical Development (from early First in Human to late clinical phases) in your region. Under guidance of the Head CQA Operations in the respective geographical region, you are responsible for the execution and performance of the Global CQA Quality System elements in the assigned compliance area including Management of CAPAs and Deviations, Inspection Preparation and Management, Change Management, Continuous Improvement, Compliance, Governance and Reporting, 3rd Party management, Regulatory Intelligence, Clinical IT Systems and Procedural Quality Assurance. You will partner with customers to assess and support...

GSK As an Oncology Medical Science Liaison, you will be the scientific expert for a group of medicines in the Hematology therapeutic area within the assigned territory to conduct balanced, peer-to-peer, scientific dialogue with external experts. This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: Interface and provide value across a continuum of both Internal and External Stakeholders (External Experts and other healthcare professionals within assigned geography/therapy area, investigators and potential investigators, and formulary decision makers) in a non-promotional manner and be responsive to unsolicited inquires. Respond orally or by providing appropriate written materials to unsolicited requests for on- or off-label information or safety concerns that may have been asked of GSK sales staff or Medical and adhering to all policies and procedures regarding the provision of...

Merck Job Description The Clinical Research Director (CRD) is the Clinical Operations lead in a country/cluster and is responsiblefor execution of all Clinical Trials in scope for GCTO country operations. Adherence to GCP, local and global policies and procedures to conduct high-quality, inspection readystudies is essential. The position is accountable for trial quality and audit responses and completion ofCAPAs. The incumbent ensures a single point of contact for managing clinical trial execution in all itsaspects across phases in scope of GCTO within the country/cluster. The position has multiple touch points across the company which will be dependent on country/clusterand the study type and stage. CRD is the primary country/ cluster level contact for GCTO and has the following key responsibilities: Supports the regional GCTO leadership team, leading strategic development of their country /cluster to deliver clinical trials as per global clinical research...

Syneos Health Description Clinical Research Associate I Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: WORK HERE MATTERS...

University of Michigan How to Apply A cover letter is required for consideration for this position and should be attached as the first page of your resume. The cover letter should address your specific interest in the position and outline skills and experience that directly relate to this position. Job Summary The University of Michigan Medical School Office of Graduate and Postdoc Studies (OGPS) and the Office of Research foster an environment of innovation and integrity that serves the Medical School research community and supports biomedical science from insight to impact. To that end, our team is constantly striving to enhance the research enterprise, including maintaining an investigator-focused infrastructure, facilitating and diversifying investigators' avenues for funding, and streamlining research processes. The UMMS Office of Research has numerous programs to position our researchers for success. The Grant Services & Analysis Office (GS&A) in partnership...

University of Michigan How to Apply A cover letter is required for consideration for this position and should be attached as the first page of your resume. The cover letter should address your specific interest in this role and outline your skills and experience that relate to this position. Job Summary The Michigan Youth Violence Prevention Center (MI-YVPC) is seeking a highly motivated and qualified candidate to provide project management support to a Centers for Disease Control (CDC)-funded research center focused on youth gun violence prevention. The selected candidate will assist with evaluations of grassroots, youth-driven gun violence prevention programs. Working in close communication with local staff and community partners, the selected candidate will take a leadership role in coordinating data collection activities at our study site in Muskegon, MI. They will contribute to qualitative and quantitative data analyses and writing up findings. The selected candidate...

Site Name: USA - Pennsylvania - Upper Providence Posted Date: Dec 4 2024 We are seeking a highly motivated Scientific Leader with expertise in Hepatitis B Virus (HBV) to join the Infectious Disease Research group in Upper Providence, Pennsylvania. In this role, you will be responsible for writing and reviewing non-clinical virology regulatory documents and conducting non-clinical laboratory studies supporting a late-stage asset. The ideal candidate will have extensive experience in non-clinical virology and regulatory report writing, a strong background in HBV, and the ability to independently manage complex projects. Key Responsibilities : Regulatory Document Preparation Author, review, and finalize high-quality non-clinical virology regulatory documents including but not limited to Non-clinical Study Reports, Investigator Brochures, Briefing Documents, and sections of regulatory submissions (e.g., NDAs, MAAs). Laboratory Studies: Conduct laboratory studies to...

University of Michigan How to Apply A cover letter is required for consideration for this position and should be attached as the first page of your resume. The cover letter should address your specific interest in the position and outline skills and experience that directly relate to this position. Job Summary The Department of Psychiatry is seeking a Research Assistant to support several mixed-methods and randomized clinical trial studies focused on suicide prevention in adults. In this role, you'll assist with NIH and VA funded research projects conducted in inpatient psychiatric settings at Michigan Medicine and the Ann Arbor VA hospitals. You will work in an exciting environment which provides support for professional growth activities and potential opportunities to submit and present at professional conferences in collaboration with the Principal Investigator and research team. Notably, you will be doing work that has real impact on patients' lives. Why Join Michigan...

University of Michigan How to Apply A cover letter is required for consideration for this position and should be attached as the first page of your resume. The cover letter should address your specific interest in the position and outline skills and experience that directly relate to this position. Job Summary The Michigan Nanotechnology Institute for Medicine and Biological Sciences (MNIMBS) is seeking a Research Lab Specialist Associate to study the immunological mechanisms of adjuvants for the development of improved vaccines. The ideal candidate will have experience in basic cellular and molecular biology/biochemical techniques including mammalian cell culture, qPCR, protein expression and purification, and immunological techniques such as ELISA, and flow cytometry. Prior experience working with mice is highly preferred. Primary responsibilities include assisting in experimental work for ongoing projects, compiling, analyzing, and interpreting results. The candidate...

Site Name: UK - Hertfordshire - Stevenage, GSK HQ, Upper Providence, USA - Massachusetts - Waltham, Warsaw Rzymowskiego 53, Zug House Posted Date: Dec 4 2024 Are you interested in a leadership opportunity to drive the implementation of effective Clinical Oncology strategies for a multi-national pharmaceutical company? If so, this role may be for you! As Clinical Development (Oncology) Director, you will be responsible for leading GSK medium and long-term oncology development strategies for GSK’s oncology pipeline. You will work closely with the Global Oncology Research and Development and Medical Affairs to ensure that the oncology clinical team have the highest quality capabilities and expertise. You will also ensure the optimal launch of new products and appropriate optimal patient use of currently available GSK Medicines through leadership and collaboration. Responsibilities: • Provide scientific input during protocol development, oversight of study conduct, and...