Physician Liaison Resume Example
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PHYSICIAN LIAISON
Professional Summary
Competent Physician Liaison & Clinical Research Monitor with Five years experience in Clinical Research and Healthcare Management. Well-developed professional skills in complex problem resolution involving synthesis, formulation, processes, testing and root cause. Articulate communicator with the ability to explain complex topics to peers and management relating to testing, research and development tasks. Credentialed Electronic Health Record Specialist experienced in paying great attention to details while managing projects related to software tools installation and end user computing.
Clinical Research Therapeutic Knowledge
- Endocrinology (5Yrs) - Diabetes (Phase I, II, III & IV).
- Infectious Diseases (2Yrs) - Hepatitis C (Phase I & IV), Influenza (Phase II).
- Oncology (5yrs) - Glioblastoma (Phase I & III - Device), Hodgkin\'s Lymphoma (Phase II), Lung (Phase III), Multiple Myeloma (Phase II).
- CNS (5Yrs) - Depression (Phase III), Schizophrenia (Phase II), Bipolar (Phase II).
- Musculoskeletal (3Yrs) - Back Pain/Pain Management (Phase III), Rheumatoid Arthritis (Phase II).
- Women\'s Health (2Yrs) - Contraception (Phase III).
Skills
|
Work History & Experience
Physician Liaison01/2017
to Current
Ascension Health – Shelby , MI
Ascension Health – Shelby , MI
- Effectively served as primary liaison for HMS and client, provider, lobbyists and partners.
- Maintained and monitored the server room, the wireless network and other server infrastructure.
Physician Liaison/CPOE Support Specialist05/2016
to 12/2016
St. Jude Children's Research Hospital – Memphis , TN
St. Jude Children's Research Hospital – Memphis , TN
- Guided Physicians on the Admission, Transfer, and Discharge patient workflow.
- Educated physicians on how to effectively use CPOE -Order Entry and Order Sets, setting up end-user In-basket pools, and setting up Favorite Smart-text templates.
- Work closely with the IT department troubleshooting physician technical computer issues including hardware, desktop, software, and other IT initiatives.
- Represented physician concerns related to new EMR, and relayed concerns and suggestions to assist with future EMR build.
- Assisted with Epic EMR implementation and Go Live support.
- Built relationships with physician\'s offices, hospitals, and skilled nursing facilities, and in turn facilitated communication between all facilities.
- Recommended that marketing materials be bilingual which was then implemented.
- Improved physician understanding to new hospital policies by strategically relaying expectation to physicians regarding policy development,.
- Contributed to the improvement of physician and patient satisfaction by enhancing partnership strategies with key leaders within the HealthCare system to provide quality service,.
- Assisted in the development includes lecture programs, employee engagement, and community efforts that enhanced and fostered positive relationships.
- Maintained good communication between department heads, medical staff and governing boards by attending board meetings and synchronizing interdepartmental functions.
- Routinely collaborated with department managers to correct problems and improve services.
- Investigated, provided and submitted information to Quality Department about special incidents, events and complaints.
Clinical Research Associate III06/2012
to 04/2016
Beacon Health Management
Completed project activities associated with monitoring functions of Phase I-IVclinicalresearch studies while developing an understanding of the drug development process, GoodClinicalPractices, and relevant regulations. Worked closely with Program Managers to allocate and assign appropriate clinical resources to monitor and manage studies/projects. Performed management of study site activities to ensure the integrity ofclinicaldata, in adherence to all applicable regulatory guidelines and Standard Operating Procedures (SOPs) and Project Specific Operating Procedures (PSOPs). Performed clinicaltrial initiation, monitoring and closeout activities while adhering to all applicable regulatory, Standard Operating Procedures (SOPs) and Project Specific Operating Procedures (PSOPs). Ensured proper work flow involving the proper conduct of studies in accordance with Good Clinical Practices, International Harmonization Guideline, and Standard Operating Procedures. Maintained oversight and direct supervision of CRAs assigned to clinical studies.Assisted with study start-up activities, site selection, and pre-study activities to identify and evaluate potential investigators. Assisted in submission of documents to the Ethics Committees, when required. Collects, reviews, and tracks regulatory documents when required.Oversaw and fixed all assigned studies within the clinical programs, including clinical schedule of tasks, timelines and priorities that aligns with the project plan. Effectively communicated changing priorities, within the team and other relevant parties, as studies and programs progress. Assisted in the development of study specific monitoring plan, annotated CRFs, monitoring conventions, tracking forms, and other study related documents. Assisted with the preparation and coordination of investigator meetings and attends meeting. Completes pre-study visits with study site staff. Completes initiation visits with study staff through training reviewing regulatory requirements, collecting outstanding documents, reviewing patient screening/randomization procedures, reviewing SAE reporting requirements, and reviewing drug storage and accountability procedures. Assisted in development of patient enrolment strategies with the project team and study site coordinator. Ensured proper storage, dispensation, and accountability of all investigational products and trial related materials. Completed monitoring visits to ensure the integrity ofclinicaldata and appropriate follow up procedures, including source document verification and SAE reporting in accordance with the project plan. Maintained tracking records for assigned sites such as tracking of status and source document review per patient.
Beacon Health Management
Completed project activities associated with monitoring functions of Phase I-IVclinicalresearch studies while developing an understanding of the drug development process, GoodClinicalPractices, and relevant regulations. Worked closely with Program Managers to allocate and assign appropriate clinical resources to monitor and manage studies/projects. Performed management of study site activities to ensure the integrity ofclinicaldata, in adherence to all applicable regulatory guidelines and Standard Operating Procedures (SOPs) and Project Specific Operating Procedures (PSOPs). Performed clinicaltrial initiation, monitoring and closeout activities while adhering to all applicable regulatory, Standard Operating Procedures (SOPs) and Project Specific Operating Procedures (PSOPs). Ensured proper work flow involving the proper conduct of studies in accordance with Good Clinical Practices, International Harmonization Guideline, and Standard Operating Procedures. Maintained oversight and direct supervision of CRAs assigned to clinical studies.Assisted with study start-up activities, site selection, and pre-study activities to identify and evaluate potential investigators. Assisted in submission of documents to the Ethics Committees, when required. Collects, reviews, and tracks regulatory documents when required.Oversaw and fixed all assigned studies within the clinical programs, including clinical schedule of tasks, timelines and priorities that aligns with the project plan. Effectively communicated changing priorities, within the team and other relevant parties, as studies and programs progress. Assisted in the development of study specific monitoring plan, annotated CRFs, monitoring conventions, tracking forms, and other study related documents. Assisted with the preparation and coordination of investigator meetings and attends meeting. Completes pre-study visits with study site staff. Completes initiation visits with study staff through training reviewing regulatory requirements, collecting outstanding documents, reviewing patient screening/randomization procedures, reviewing SAE reporting requirements, and reviewing drug storage and accountability procedures. Assisted in development of patient enrolment strategies with the project team and study site coordinator. Ensured proper storage, dispensation, and accountability of all investigational products and trial related materials. Completed monitoring visits to ensure the integrity ofclinicaldata and appropriate follow up procedures, including source document verification and SAE reporting in accordance with the project plan. Maintained tracking records for assigned sites such as tracking of status and source document review per patient.
Clinical Rotation-Medical Student Clinical Research Assistant (Unpaid)01/2011
to 05/2012
Atlanta Medical Center
Assisted in the management of daily activities of a clinical team consisting of physician, nurses and support staff. Experience in explaining treatment procedures to patients, preparing patients for examination, assisting the physician during exams, and instructing patients about medication and special diets. Investigated and reported issues relating to patient conditions that might hinder patient well-being whiled enrolled in research study. Coordinated the allocation of research study equipment and supplies within the facility and established guidelines for efficient and economical use. Interpreted and communicated new or revised policies to staff. Assisted in accurate completion of forms/reports for each study subject.
Participated in clinical trial
activities as a medical student research assistant at Investigative sites
and Hospitals.Experience in maintaining a safe
and clean working environment by complying with procedures, rules, and
regulations. Complied with federal, state,
and local legal and professional requirements by studying and abiding to existing
and new legislation such as Good Clinical Practices, and advising management on
needed actions.
Experienced
in patient interview, vital signs, including weight, blood pressure,
pulse, temperature, and documentation of information in patient\'s chart.
Experienced
in ensuring related reports, labs and information files are available in
patients\' medical records.
Participated inclinical monitoring and activities
while adhering to all applicable regulatory authorities, and Standard
Operating Procedures.
Participated in the development of study specific monitoring
plan, annotated CRFs, monitoring conventions, tracking forms, and other
study related documents.
·
Atlanta Medical Center
Medical Student Clinical Rotation01/2011
to 05/2012
Atlanta Medical Center – Estherville , STATE
Atlanta Medical Center – Estherville , STATE
Medical Student Clinical Rotation01/2010
to 12/2010
St. Joseph Hospital – City , STATE
St. Joseph Hospital – City , STATE
Emergency Room Volunteer01/2006
to 05/2006
Jesse Brown VA Medical Center – City , STATE
Jesse Brown VA Medical Center – City , STATE
Pharmacy Technician Assistant03/2005
to 01/2006
Walgreen Pharmacy – City , STATE
Walgreen Pharmacy – City , STATE
Certified Nursing Assistant 11/2003
to 05/2004
Loving Care Svc Inc – City , STATE
Loving Care Svc Inc – City , STATE
Education
Master of Public Health: Public HealthMay 2016Walden University-
City,
State
MBA: HealthCare AdministrationDec 2012Walden University-
City,
State
Doctor of Medicine degree: May 2012Avalon University School of Medicine-
City,
State
- Graduated Magna Cum Laude (Doctor of Medicine)
Bachelors degree: Biological SciencesMay 2007University Of Illinois at Chicago-
City,
State
Affiliations
American Public Health Association
Certifications
Doctor of Medicine CertificationAdvanced Cardiac Life Support CertificationCredential Electronic Medical Record Specialist
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Resume Overview
School Attended
- Walden University
- Avalon University School of Medicine
- University Of Illinois at Chicago
Job Titles Held:
- Physician Liaison
- Physician Liaison/CPOE Support Specialist
- Clinical Research Associate III
- Clinical Rotation-Medical Student Clinical Research Assistant (Unpaid)
- Medical Student Clinical Rotation
- Emergency Room Volunteer
- Pharmacy Technician Assistant
- Certified Nursing Assistant
Degrees
- Master of Public Health : Public Health May 2016
MBA : HealthCare Administration Dec 2012
Doctor of Medicine degree : May 2012
Bachelors degree : Biological Sciences May 2007
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