- Highmark Health (Augusta, ME)
- …Coder (CPC) + Certified Outpatient Coder (COC) + Accredited Healthcare Fraud Investigator (AHFI) **SKILLS** + Must have knowledge of provider facility payment ... methodology, claims processing systems and coding and billing proficiency + Must have understanding of technical and financial aspects of the health insurance industry + Strong personal computer skills, along with the ability to use fraud/abuse data mining… more
- Meta (Augusta, ME)
- …to protect Meta users from harm. **Required Skills:** Technical Investigator , Integrity Operations Responsibilities: 1. Apply quantitative skills and incorporate ... qualitative insights to inform and influence strategy for Integrity Operations 2. Investigate complex cases to understand in granular detail how abuse is occurring and attribute the person(s) responsible. Identify and implement appropriate online and offline… more
- TD Bank (Lewiston, ME)
- …Management **Job Description:** The Senior AML Financial Crime Risk Investigator conducts complex investigations into potential money laundering, terrorist ... financing, and other financial crimes, including insider-risk matters. This role requires a deep understanding of AML regulations, strong writing and analytical skills, and the ability to work collaboratively with internal and external stakeholders. **Depth &… more
- Merck (Augusta, ME)
- …activities including our Company's sponsored trials and our Company's Independent Investigator Study Programs as prioritized and requested by our Research & ... activities including our Company's sponsored trials and our Company's Independent Investigator Study Programs as prioritized and requested by our Research &… more
- Merck (Augusta, ME)
- …for approved, in-development, and active Company-sponsored trials and/or investigator -sponsored research studies. The Regional Medical Scientific Director serves ... Enhances the comprehension of the scientific foundations and goals of investigator -sponsored research. + Identifies barriers to patient enrollment and retention… more
- Sumitomo Pharma (Augusta, ME)
- …Forms (ICF), Safety Management Plans (SMP), Clinical Study Reports (CSR), Investigator 's Brochures (IB), Investigator communications (Dear Health Care Provider ... + Participates/contributes to other activities such as literature evaluation, investigator site training, continuing education for internal staff, inspection/audit… more
- Bausch + Lomb (Augusta, ME)
- …updates on progress and changes in scope, schedule, and resources. + Organize investigator and expert meetings relevant to the indication and assist with the ... handled by the CRAs and responded to by the site/ investigator in a timely manner. May assist in the...discuss study related issues and problems with the Principal Investigator and/or site staff. + Share/present knowledge and information… more
- Otsuka America Pharmaceutical Inc. (Augusta, ME)
- …late-breaking clinical trial sessions + Sponsored symposia and educational sessions + Investigator meetings and closed sessions + Booth design and scientific content ... opinion leaders before, during, and after congresses + Organize and facilitate investigator meetings and advisory boards in conjunction with congresses + Create… more
- Otsuka America Pharmaceutical Inc. (Augusta, ME)
- …Otsuka's clinical trials program, including registrational, post-marketing and Investigator -Sponsored Trials (ISTs), health economic outcomes research, other ... specific medical collaborations; provide clinical expertise and feedback regarding operational management of clinical trials to ensure optimal site selection and performance. + Support other areas of the organization including Safety & Pharmacovigilance for… more
- Sumitomo Pharma (Augusta, ME)
- …+ Provide support for advisory boards, consultant meetings, and investigator meetings, including preparation and/or delivery of presentations. + Understand ... the competitive landscape and provide insights on strategic development pathways. + Keeps abreast of oncology treatment modalities, drug mechanism of action, approaches to drug development, and regulatory requirements. + As appropriate, coach and guide less… more
- Sumitomo Pharma (Augusta, ME)
- …intended for regulatory submission. For example, clinical study reports (CSRs), investigator brochures (IB), new drug application (NDA) common technical document ... (CTD) non-clinical drug metabolism, bioanalytic, and clinical pharmacology chapters, and alike. + Support clinical protocols and protocol execution, including lab manual authoring based on information received from bioanalytic laboratories, pharmacokinetic… more
- Pfizer (Augusta, ME)
- …populations in trials + Appropriately provide Medical support throughout the Investigator Sponsored Research (ISR) process + Cultivate research and therapeutic area ... expertise, including familiarity with latest congress data and disease state literature + Provides Asset leadership + Understand the principles of study design, methodology, data analysis, and interpretation and communicate these concepts with customers +… more
- Merck (Augusta, ME)
- …of local data generation study concepts and protocols. + Reviews Investigator -Initiated Study proposals from key countries prior to headquarters submission (ex-USA). ... + Manages programs (patient support, educational or risk management) to support appropriate and safe utilization of Our Company medicines or vaccines. **Required** **Qualifications** **, Skills & Experience:** **_Minimum:_** + MD, Ph.D., Pharm.D., or OD (MD… more
- Merck (Augusta, ME)
- …of local data generation study concepts and protocols + Reviews investigator -initiated study proposals prior to headquarters submission (ex-USA) + Manages regional ... programs (patient support, educational or risk management) to support appropriate and safe utilization of Our Company's medicines **Required** **Qualifications** **, Skills & Experience:** **_Minimum:_** + MD, PhD, PharmD or OD (MD preferred) and recognized… more
- Merck (Augusta, ME)
- …USMA's five functional pillars (1. Scientific Exchange; 2. Company Trials; 3. Investigator Sponsored Programs 4. Congresses; 5. Insights). The SDMA is an experienced ... therapeutic area leader/ subject matter expert with experience in Immunology who possesses relevant medical affairs and field medical (FM) experience to guide and direct field medical strategy and anticipate regional FM needs in alignment with US/global… more
- Sumitomo Pharma (Augusta, ME)
- …Provide strategy and oversight for the development of a supportive US Investigator Initiated Study and Collaborative Research program. + Provide detailed and ... compliant medical review and approval of external resources, communications, and publications - ensuring medical accuracy, relevance, and fair-balance. + Develops and oversees Medical Affairs annual operating budget. + Manages direct reports (if assigned). +… more
- Otsuka America Pharmaceutical Inc. (Augusta, ME)
- …of clinical facility and system audits at all relevant facilities, investigator sites, and vendors (including contract research organizations) and ensure that ... audit results are communicated, and appropriate corrective actions are implemented and documented on a timely basis. + In addition, this role is responsible for establishing standards and implementing procedures to ensure that the business units quality… more
- Otsuka America Pharmaceutical Inc. (Augusta, ME)
- …pharmacology** sections for regulatory filings, including annual reports, investigator 's brochure, IND/NDA/BLA applications and pediatrics development plans in ... compliance with relevant guidelines and standards. + Work with pharmacometricians, support **model-based drug development (MIDD)** strategies, and provide input to PK and PK/PD modeling analysis to support dose selection, efficacy and safety assessments. +… more