https://www.bchrs.com/advantage daily 0.75 2022-04-07 https://images.squarespace-cdn.com/content/v1/5fa83ae2b1558e3d0560381c/1606174864237-IMG1MCJ1X530LMD4ZEMN/shutterstock_68504584.jpg BCH Advantage - PROVIDE EARLY PHASE RESEARCH EXPERTISE Our in-depth knowledge of both the scientific and operational aspects of early phase trials makes BCH stand out among other clinical research service providers. We are sought after by clients for the ability to apply our knowledge of clinical pharmacology to a wide variety of projects involving program strategy, study operations, medical writing, and submission support. This knowledge base and skill-set operating together in a sleek, small company environment make us extremely efficient and enable us to deliver great value to our clients; high quality services delivered in shorter times and at a lower cost than the industry average. https://images.squarespace-cdn.com/content/v1/5fa83ae2b1558e3d0560381c/1606174785886-DR1M4SUK02L7BU71OF82/shutterstock_1508142638.jpg BCH Advantage - PROVIDE CLINICAL RESEARCH OPERATIONS AND MEDICAL WRITING SUPPORT FOR PHARMACEUTICAL COMPANIES Managing the dynamic workload in R&D continually challenges the pharmaceutical industry regardless of a company's size. BCH provides your organization with a new, more efficient, strategic resourcing solution than traditional flexible staffing arrangements. BCH is comprised of experienced pharmaceutical research professionals with expertise in early drug development, who can step in quickly and independently complete a single project or support an entire program for your business with limited use of your in-house resources. https://images.squarespace-cdn.com/content/v1/5fa83ae2b1558e3d0560381c/1606174952016-MR03M4JAAM3C6D3XOTVO/image-asset.jpeg BCH Advantage - PROVIDE CLINICAL RESEARCH UNITS WITH EXPANDED CAPABILITIES Clinical Research Units (CRUs) may be asked by sponsors to function as full-service CROs and provide end-to-end services for the implementation of clinical trials. BCH can help your CRU accomplish this by assembling a team of experts in the fields of data management, biostatistics, and site monitoring. BCH manages the administrative and operational aspects of the trial from protocol writing through authoring of the final study report, allowing CRUs to focus on what you do best - the clinical implementation of trials and the medical care and safety of patients. https://www.bchrs.com/about-us daily 0.75 2022-04-07 https://images.squarespace-cdn.com/content/v1/5fa83ae2b1558e3d0560381c/1606147642890-5SYV8LCJQQSHQJ3LCRXL/DSC_0013v2.jpg About Us - Make it stand out Whatever it is, the way you tell your story online can make all the difference. https://images.squarespace-cdn.com/content/v1/5fa83ae2b1558e3d0560381c/1622574371814-6VTEYBSECPMZFLKHCD29/P10.jpg About Us - Make it stand out Whatever it is, the way you tell your story online can make all the difference. https://images.squarespace-cdn.com/content/v1/5fa83ae2b1558e3d0560381c/1605702196744-Q5YSPWEEUDMWFKIBZ9FB/blob.png About Us https://images.squarespace-cdn.com/content/v1/5fa83ae2b1558e3d0560381c/1605701865511-PASNEUGCC8JGKFJR7XWE/eersupply%2Bco..png About Us https://www.bchrs.com/privacy-policy daily 0.75 2021-05-12 https://www.bchrs.com/home daily 1.0 2022-04-19 https://images.squarespace-cdn.com/content/v1/5fa83ae2b1558e3d0560381c/1642788816433-LX2G31ACO006AI8ZS8NL/GettyImages-1144287280.jpg Home https://images.squarespace-cdn.com/content/v1/5fa83ae2b1558e3d0560381c/1606174098712-T8OPPT5VRNBBHAE2KKTV/image-asset.jpeg Home https://images.squarespace-cdn.com/content/v1/5fa83ae2b1558e3d0560381c/1642789308424-026XZR0I447XKBGRI7HZ/GettyImages-1141464027.jpg Home https://images.squarespace-cdn.com/content/v1/5fa83ae2b1558e3d0560381c/1642789665736-5S8JLVD6TZB6H37M8M9E/GettyImages-1147384767.jpg Home https://www.bchrs.com/bch-advantage daily 0.75 2020-11-16 https://www.bchrs.com/scientific-medical-writing daily 0.75 2022-04-07 https://images.squarespace-cdn.com/content/v1/5fa83ae2b1558e3d0560381c/1605708158207-LKZ088BG8GJRF45KM4YI/image-asset.jpeg Scientific Medical Writing - SCIENTIFIC MEDICAL WRITING BCH utilizes industry-leading templates to produce ICH compliant, submission-ready documents. BCH can also author documents using your company's templates as requested. https://images.squarespace-cdn.com/content/v1/5fa83ae2b1558e3d0560381c/1606175139749-1VHSAFMFFYMWGV1CPRVW/image-asset.jpeg Scientific Medical Writing - Clinical trial documents we author include: Protocols and protocol amendments Full and abbreviated Clinical Study Reports Investigator Brochures Informed Consent Forms Development Safety Update Reports IND clinical sections CTD clinical sections Briefing Books for agency meetings https://www.bchrs.com/clinical-research-operations daily 0.75 2022-04-07 https://images.squarespace-cdn.com/content/v1/5fa83ae2b1558e3d0560381c/1606175377324-CLB25G5LO8PS7X8S1OP7/image-asset.jpeg Clinical Research Operations - CLINICAL TRIAL OPERATIONS AND CONSULTING Clinical Operations Leadership Clinical Compliance/GCP Expertise Clinical Supplies/GMP Expertise Clinical Site Monitoring Clinical Data Review Vendor selection and management Clinical Operations SOP Review and Development https://images.squarespace-cdn.com/content/v1/5fa83ae2b1558e3d0560381c/1606175314591-WBBOPLLJO4ZQ45H4PYLN/image-asset.jpeg Clinical Research Operations - THERAPEUTIC AREA EXPERIENCE Allergy/Immunology Cardiovascular Endocrinology Gastrointestinal Hematology Immunodeficiency Infectious Disease Metabolic Disorders Neurology Ophthalmology Vaccines https://www.bchrs.com/consulting daily 0.75 2022-04-19 https://images.squarespace-cdn.com/content/v1/5fa83ae2b1558e3d0560381c/1606014514469-J6C04ELS8ATL6NA2MXI8/image-asset.jpeg Consulting - BCH facilitates effective and efficient implementation of early phase clinical research programs Program-level support or individual study support Project management of in-house or outsourced activities Development of specific project processes, responsibilities, and communication plans Maintenance and reporting of timelines Support for audit preparation, responses, and action plans Clinical SOP review and development Process improvement https://images.squarespace-cdn.com/content/v1/5fa83ae2b1558e3d0560381c/1606012894478-HE2CLUYOKFVQTL1OBNFN/image-asset.jpeg Consulting BCH always keeps study participant safety at the forefront of strategy while working to meet individual trial objectives. BCH implements trial processes carefully with attention to detail resulting in accurate data sets suitable for expert analysis. https://www.bchrs.com/project-management daily 0.75 2022-04-07 https://images.squarespace-cdn.com/content/v1/5fa83ae2b1558e3d0560381c/1622568746658-MKRBAI7XBYWACAKDZOQY/shutterstock_1666851595.jpg Project Management - Project Management Sponsor program and study management: Development, maintenance, and reporting of project timelines Vendor coordination and oversight Development of specific program and project plans Process improvement/efficiency evaluation and support https://www.bchrs.com/news daily 0.75 2022-04-07 https://images.squarespace-cdn.com/content/v1/5fa83ae2b1558e3d0560381c/1606176205596-50ZRUBSGH64204OCU7YC/HBALogoGlobal_RGB_72dpi.jpg News https://images.squarespace-cdn.com/content/v1/5fa83ae2b1558e3d0560381c/1606176179630-VKRJNB0DEPBI6MHZ3SU3/eersupply%2Bco..png News https://www.bchrs.com/contact daily 0.75 2022-01-21 https://images.squarespace-cdn.com/content/v1/5fa83ae2b1558e3d0560381c/1606146790711-O4J6FACE1GBKQJQRSCJA/shutterstock_717315007.jpg Contact https://www.bchrs.com/partners daily 0.75 2021-06-01 https://images.squarespace-cdn.com/content/v1/5fa83ae2b1558e3d0560381c/1622572737311-7CWBW5WII272AF1208SW/DSC_0013v2.jpg Partners - Janet Boyle Co-founder and Compliance Officer BA Biology/Health & Human Development; Lehigh University MS Clinical Research Organization & Management; Drexel University College of Medicine 3 years experience in Merck Manufacturing Division: Biological Quality Control Inspector and Supervisor, Environmental Compliance 10 years experience with BCH and 18 years experience at Merck in Phase I-III Clinical Research including all aspects of study conduct, regulatory document writing (protocols, IBs, CSRs), data review/management, and regulatory filing activities including Integrated Summaries of Safety & Efficacy. Contributed to multiple drug development programs in several therapeutic areas. Personnel and program management resource allocation for Early Clinical Research portfolio (200+ studies), program-wide CSR and WMA planning and tracking. Initiative leader and contributor for large pharma merger roles and operations and process harmonization teams. https://images.squarespace-cdn.com/content/v1/5fa83ae2b1558e3d0560381c/1606150850596-8JOVAUFV9MG3GVVSPE6W/P10.jpg Partners - Michele Hyman Co-founder and Operations Officer BS Pharmacy/University of the Sciences Philadelphia 9 years experience in GMP, marketed and research material; manufacturing, packaging, and global clinical supplies coordination 2 years experience in clinical research process, training, and personnel development as a clinical learning development specialist 10 years experience with BCH and 14 years experience at Merck in Early Phase Clinical Research including: Protocol authoring and all aspects of study conduct and site coordination, regulatory document writing, data management, report writing, and filing activities -contributing to multiple drug development programs in several therapeutic areas. Personnel and program management, resource allocation for large early clinical research portfolio. Initiative leader and contributor to departmental company merger teams and leader for the departmental Training, Development, and Curriculum Team, as well as, multiple process and system development teams.