Raymond Panas Email and Phone Number
Pittsburgh, PA, US
Raymond Panas's Location
Pittsburgh, Pennsylvania, United States, United States
Raymond Panas's Contact Details
Raymond Panas work email
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Raymond Panas phone numbers
About Raymond Panas
Experienced Director and Faculty with demonstrated skills in Medical Affairs, Program Leadership, Program Management, Research Operations, Health Education/Communications, and Academic Instructor with a working knowledge of pharmaceutical research, public health, and higher education. Strong education and professional skills in Electronic Data Capture (EDC), Good Clinical Practice (GCP), Clinical Monitoring, Medical Affairs, Public Health, and Pharmacovigilance. • Program Leadership – Develop new programs to support institutional and corporate efforts. Establish policies and procedures to create effective operations. Conduct analyses to ensure efficiencies. • Research Management - Extensive experience in national and international program management. Skilled in the development, implementation, and supervision of budgets, timelines, vendors and research activities. Utilized patient reported outcome measures for research methods and published reports. • Health Communications - Developed medical education materials for trainings and presentations. Worked with patient advocates and industry groups for congressional support for health issues. Provided educational sessions for physicians, employees, and students about diseases and public health issues. • Facilitator - Effective communicator with individuals, key opinion leaders, and regulators through personal and electronic interaction. Author and presenter for posters, presentations and publications.Qualified academic instructor and presenter via oral, print, and electronic methods.
Raymond Panas's Current Company Details
University Of Pittsburgh Graduate School Of Public Health
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Adjunct Assistant Professor
Pittsburgh, PA, US
- Website:
- pitt.edu/pittwire
- Employees:
- 19244
Raymond Panas Work Experience Details
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Adjunct Assistant ProfessorUniversity Of Pittsburgh Graduate School Of Public HealthPittsburgh, Pa, Us
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Senior Medical Science LiaisonInflarx N.V.Pittsburgh, Pa, Us -
Senior Medical Science LiaisonInflarx N.V. Jul 2023 - PresentJena, De• Serve as disease state and scientific expert from commercial and developmental products.• Provide scientific presentations to physicians, healthcare providers, staff, and key opinion leaders.• Establish relationships to support the scientific exchange of information and shared initiatives.• Support product launch through review of FDA filing and training for corporate scientific education.• Develop and present materials for internal medical, research, and commercial teams.• Serve as liaison for non-/government relations, legislative affairs, and foundation support.• Develop clinical white papers and publications with key opinion leaders on key scientific information. -
Adjunct Assistant ProfessorUniversity Of Pittsburgh Graduate School Of Public Health Jun 2021 - PresentPittsburgh, Pa, UsAdjunct Faculty in the Graduate School of Public Health, Department of Behavioral and Community Health Science. -
Senior Contributing FacultyWalden University Mar 2009 - PresentUs• Faculty for the Public Health and Clinical Research Administration programs.• Instruct online courses within the College of Health Sciences.• Serve as the Dissertation Advisor for over 25 doctoral students.• Facilitate the submission of materials for IRB Review, Project Review, and Dissertation Approval.• Inductee into the National Society of Leadership and Success (2019).• Promoted to Senior Contributing Faculty (Nov. 16, 2018). -
Research Health ScientistPittsburgh Va Healthcare Systems Apr 2021 - Sep 2024• Serve as Program Manager to the Principal Investigator of MIRECC Peer Resources Center• Provide administrative leadership to the research projects and manage the research teams.• Establish/track/report on programs, research activities, performance, budgets, and timelines.• Ensure research is conducted according to the protocol, SOPs, and ICH/GCP regulations and study procedures.• Prepare/review materials for grant submissions, project budget modifications, and regulatory submissions. -
Senior Director, Clinical & Research OperationsLygenesis Jun 2020 - Apr 2021Pittsburgh, Pennsylvania, Us• Program leader responsible for oversight of clinical trial operations and development of clinical program.• Provide support to the preclinical development for transition to clinical development program.• Develop/contribute to preparation of clinical protocols, amendments, informed consent forms, study guides, case report forms, clinical study reports, regulatory filings, and any other research related document.• Establish/track/report on clinical programs, research activities, site performance, budgets, and timelines.• Manage CROs, contracted vendors, and investigational sites for proper conduct of clinical studies.• Ensure research is conducted according to the protocol, SOPs, and ICH/GCP regulations and study procedures.• Prepare materials for IND submission and address questions from regulatory authorities.• Maintaining up to date listings on Clinicaltrials.gov and Trial Master Files. -
Adjunct Assistant ProfessorGeorge Washington University Aug 2009 - Aug 2020Washington, D.C., Us• Faculty for the Department of Clinical Research and Leadership programs.• Instruct online courses within the School of Medicine and Health Sciences.• Assist in the development and updating of the online course curriculum. • Review student applications for acceptance into undergraduate and graduate programs.• Received “Educator of the Year” award by the Washington Blade in 2012.• Faculty inductee into the Alpha Eta Honor Society in 2014. -
Director Of Medical AffairsRedhill Biopharma Ltd. Jul 2017 - Jun 2020Raleigh, Nc, UsDirector of Medical Affairs (9/2018 - 6/2020)Senior Medical Science Liaison (7/2017 - 9/2018)• Senior management of medical affairs, medical education, health communication and pharmacovigilance.• Serve as disease state and scientific expert from commercial and developmental products.• Provide scientific presentations to physicians, healthcare providers, staff, and key opinion leaders.• Establish relationships to support the scientific exchange of information and shared initiatives.• Support product launch through review of FDA filing and training for corporate scientific education.• Develop and present training materials for internal medical, research, and sales teams.• Provide individualized training for physicians for company speakers’ bureau.• Serve as primary liaison for non-/government relations, legislative affairs, and foundation support.• Develop clinical white papers and publications with key opinion leaders on key scientific information. -
Program DirectorChildren'S National Health System May 2016 - Jul 2017Washington, Dc, Us• Coordinate with industry sponsors, contract research organizations and other organizations to attract clinical research projects and facilitate relationships with internal/external stakeholders.• Collaborated with operational units and leadership regarding performance metrics to enhance operations.• Identify gaps and processes using data-driven Lean and Sigma Six principles to initiate corrective measures to enhance and streamline supportive activities between research operational units.• Establish onboard training program for new research staff regarding clinical research operations.• Provide advice and counsel to senior research administration and research teams to raise awareness and demonstrate the strategic and economic importance of quality standard in the conduct of research. • Respond to inquiries regarding site capabilities, investigator specialties, and trial participation.• Created educational program to support ongoing certification of research team members. -
Senior Medical Science LiaisonEntera Health Feb 2014 - May 2016Ankeny, Iowa, Us• Provide leadership in medical affairs, medical education, and health communication.• Present at scientific roundtables to physicians, medical staff, and key opinion leaders.• Serve as primary liaison for non/government relations, legislative affairs, and foundation support.• Develop clinical white papers and support publications activities on scientifically relevant information.• Support investigator sponsored research and grant requests processes. -
Dissertation AdvisorUniversity Of Liverpool Online Jan 2010 - Apr 2015• Dissertation advisor for nearly 10 students completing their Master’s degree.• Reviewer of IRB application and submission materials.• A couple of my students have received the “Dissertation of the Year” award (2013/2014).• Awarded “Honorary Recognised Teacher” in the Institute of Learning and Teaching (2013).
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Principal ConsultantShay Research Consulting, Llc Apr 2012 - Feb 2014• Provide support for Medical Affairs, Clinical Operations, and Clinical Development activities.• Medical writing support for health communication, product information and clinical trial reports.• Provide drug development guidance to small biotech and virtual pharmaceutical company activities.• Support investigator sponsored research and grant requests processes.• Develop standard operating procedures and conduct training for clinical and medical affairs.
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Director Of Medical & Scientific AffairsSucampo Pharmaceuticals, Inc. Oct 2002 - Feb 2014Rockville, Md, Us04/2012-02/2014 - Medical Affairs Consultant04/2011-04/2012 - Director of Medical & Scientific Affairs12/2010-04/2011 - Director of Global Pharmacovigilance & Safety Surveillance07/2007-12/2010 - Director of International Clinical Development10/2004-07/2007 - Therapeutic Program Director10/2002-10/2204 - Senior Clinical Trial Manager• Established Medical & Scientific Affairs department for medical information and scientific education.• Coordinated pharmacovigilance program to a globalized system incorporating company affiliates.• Created and managed investigator-initiated research grant review and approval process.• Identified, established and maintained relationships with key opinion leaders/consultants for advisory boards, brand development, outcomes research, clinical research programs and publication activities. • Served on the Management Team for US and EU operations.• Establish multiple clinical programs/protocols and coordinate research activities, budgets and timelines.• Participated in regulatory agency meetings – FDA, EMEA, and European Health Authorities.• Prepared paper and electronic submissions (IND, NDA and MAA) for regulatory agencies.• Managed CROs, contracted vendors, and investigational sites for proper study conduct.• Clinical project leader responsible for writing clinical protocols and managing clinical trials. -
Clinical Project ManagerWellstat Therapeutics Corporation Sep 2001 - Oct 2002• Project leader responsible for developing and implementing new clinical program.• Oversaw clinical studies, protocols, budgets and timelines; develop CRF and study documents.• Coordinated the selection and management of CRO and other contracted vendors; selection of study investigators; planning and conducted study meetings and training sessions.• Oversaw the clinical monitoring and safety reporting by CRAs and the quality of the data analysis.• Coordinated consultants and scientific leaders to establish clinical program. -
Senior Clinical Research Associate - Project ManagementTap Pharmaceuticals Aug 1999 - Sep 2001Us• Senior clinical team member responsible for design and conduct of Phase I-III studies. • Project Manager of multicenter clinical studies including the study planning; protocol writing; study initiation, conduct, monitoring, closeout; data management; study analysis and report writing. • Negotiated contracts with study sites, contract research organizations, and study vendors.• Conducted co-monitoring visits with internal and contract CRA teams to ensure adherence to internal company standards and policies, regulatory requirements, and clinical protocols. -
Senior Clinical Research AssociateClintrials Research, Inc Jul 1995 - Sep 1999• Project leader responsible for multinational clinical trials: monitor study budgets, review monitoring activities of project team, evaluate subject enrollment, coordinate supplies/drug.• Worked with other department leads to assure timely completion of project activities.• Planned and managed activities for site selection, investigator meeting, and enrollment.• Supervised, evaluated, and mentored CRAs and established goals for team members.• Developed informed consents, case report forms, monitoring guidelines and site materials. • Attended project management meetings to ensure the maintenance of budgets and timelines.• Conducted project team meetings to review project status, budget, timelines, and site/team issues.• Oversaw compliance of studies with FDA regulations, Good Clinical Practices, and protocols • Mentored new employees and taught department training modules for employees.• Developed inform consents, case report forms, site training materials, and monitoring tools. • Conducted project team meetings to review project status, project team issues, and site issues.• Conducted site-monitoring visits to ensure the accuracy and accountability of clinical data through the review of case report forms, source documents, and medical records.• Ensured compliance with FDA regulations, Good Clinical Practices, and study protocols.
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Aids Specialist / MicrobiologistAllegheny County Health Department Jul 1989 - Aug 1995Pittsburgh, Pa, Us• Supervised the daily activities of the HIV/AIDS screening lab and flow cytometry lab.• Established flow cytometry lab for the testing and monitoring of T-cells for monitoring immune status.• Performed EIA/ELISA tests for HIV screening, and Western Blot or IFA confirmation tests.• Trained and certified technicians on the performance of various testing methods.• Communicated and dealt with a variety of healthcare professionals and agencies.• Provided technical information assistance to outreach counselors and healthcare providers.• Provided supervision and assistance in virology, serology, and bacteriology labs as needed.
Raymond Panas Skills
Clinical Development
Pharmaceutical Industry
Clinical Research
Clinical Trials
Pharmacovigilance
Clinical Monitoring
Public Health
Medicine
Medical Affairs
Oncology
Gcp
Infectious Diseases
Biotechnology
Life Sciences
Cro
Ctms
Good Clinical Practice
Clinical Trial Management System
Cro Management
Clinical Operations
U.s. Food And Drug Administration
Clnical Research
Regulatory Affairs
Drug Development
Electronic Data Capture
Regulatory Submissions
Medical Writing
Raymond Panas Education Details
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Walden UniversityPublic Health Education & Promotion -
University Of Pittsburgh School Of Public HealthCommunity Health Services And Promotion
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University Of PittsburghBiology & Economics
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Titusville High SchoolCollege Prep
Frequently Asked Questions about Raymond Panas
What company does Raymond Panas work for?
Raymond Panas works for University Of Pittsburgh Graduate School Of Public Health
What is Raymond Panas's role at the current company?
Raymond Panas's current role is Adjunct Assistant Professor.
What is Raymond Panas's email address?
Raymond Panas's email address is ra****@****liv.onl
What is Raymond Panas's direct phone number?
Raymond Panas's direct phone number is +120232*****
What schools did Raymond Panas attend?
Raymond Panas attended Walden University, University Of Pittsburgh School Of Public Health, University Of Pittsburgh, Titusville High School.
What skills is Raymond Panas known for?
Raymond Panas has skills like Clinical Development, Pharmaceutical Industry, Clinical Research, Clinical Trials, Pharmacovigilance, Clinical Monitoring, Public Health, Medicine, Medical Affairs, Oncology, Gcp, Infectious Diseases.
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