Primary Care Project Manager

QUALIFICATIONS PROFILE

Collaborative and motivational team player, with outstanding ability to communicate and partner with colleagues and supervisors while simultaneously managing numerous independent projects successfully

Ability to observe, assess, and record symptoms, reactions, and progress

Able to communicate medical information to professional practitioners and/or the general public

Extensive knowledge of CPR, emergency medical procedures and of primary care principles and practices

Extremely skilled at making administrative and procedural decisions

Strong knowledge of drugs and their indications, dosing, side effects, and proper administration

Analytical approach to data and information management, reporting, and record maintenance

Strong technical proficiency with talent for quickly learning and applying new techniques and methods

Ability to acquire knowledge in different disease and therapeutic areas

Develop training protocols on technical aspects of proper clinical data collection for stroke program registry

Proven ability to maintain accurate results, ensuring full compliance and adherence to industry regulations and guidelines, including GCP and HIPPA

Excellent sense of patient relations in clinical setting and trained on Adverse Effect Reporting.

THERAPEUTIC EXPERIENCE

Cardiovascular:

Congestive Heart Failure

Pediatric Epilepsy

Devices: Alprazolam Inhaler Neurology

Type II Diabetes

Gastrointestinal Hemorrhage

Musculoskeletal:

Neurology Intracranial Hemorrhage

Neurology Epilepsy Tonic/Clonic Seizures

Psychiatric (Depression Disorder, Bipolar Disorder, Schizophrenia)

Respiratory Failure

Oncology

COVID 19 Vaccine

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REINA MALCOLM, FOREIGN MD

11741 SW 150th PL Miami FL, 33196

Cell 347-***-**** ************@*****.***

CLINICAL TRIALS PHYSICIAN

Accomplished and detail-oriented Physician poised to leverage related clinical expertise to excel within the healthcare setting. Demonstrated capacity to work both independently and within teams to facilitate and provide comprehensive clinical trial patient care. Possess special sensitivity in meeting diverse needs in varied situations, combined with exceptional planning, prioritizing, and goal-setting skills. Motivated, customer-focused Senior Project Manager with more than 20 years of experience at both CRO and pharma. Over 15 years’ experience managing global clinical trials over several therapeutic areas

11741 SW 150th PL Miami FL, 33196

Cell 347-***-**** ************@*****.***

PROFESSIONAL EXPERIENCE

General Administrative

• Act as primary contact with Customer throughout study. Up to delivery of final project product(s).

• Plan and implement, to achieve anticipated and unexpected project deliverables.

• Analyze and oversee cost, personnel hours and project needs to determine the most cost effective and efficient means to run and complete projects successfully on time, to agreed quality standards and within budget while meeting the Customer’s needs and adhering to the contract.

• Delegate assigned responsibilities to project team members.

• Have regular and proactive liaisons with Department Heads to optimize performance and utilization of the project members.

• Anticipate potential issues and escalate appropriately/pro-actively to their Franchise Director/Associate Director

• KPI Tracker

• Create Metrics for the studies

• Manage Concerns for the sponsor, including extra travel expenses

• Participation and attendance in bid defense process

• Provide feedback on project team members’ performance to respective line-managers

• Analysis and projections of project timelines

• Maintains adequate inventory of study supplies.

• Retains all study records in accordance with sponsor requirements and University of Miami policies and procedures.

• Maintains effective and ongoing communication with sponsor, research participants and PI during the study.

• Vendor and Agencies Management

• Primary liaison with sponsor providing oversight and accountability for clinical studies, managing budgets and timelines, resource planning, risk mitigation and adherence to SOPs and ICH/GCP guidelines

MARKEN LLC HEALTH MANAGEMENT (JOHNSON & JOHNSON VACCINE COVID19 TRIAL) SENIOR COORDINATOR LEAD FOR LATINO AMERICA-US - SEPT2020-JUNE 2022 General Administrative

• Coordinates with Sponsor JnJ, and central administration to help ensure that clinical research and related activities are performed in accordance with Federal regulations and Centers and sponsoring agency policies and procedures.

• Argentina, Mexico, Peru, Brazil and Colombia-US Lead Manager for Vaccine Covid 19 Trial .

• Coordinates and facilitates monitoring and auditing visits. Notifies appropriate institutional officials of external audits by sponsor.

• Collaborates with PI and institution to respond to any audit findings and implement approved recommendations.

• Create and maintain Trackers and Metrics: Nurse Stats, Master Priority Site list, HHCP Metrics

• Develop study plan outlining planning, execution, and closeout milestones. REINA MALCOLM, FOREIGN MD

MARKEN LLC HEALTH MANAGEMENT

SENIOR PROJECT MANAGER NORAM-LOGISTIC - JUNE 2022-CURRENT 2 of 10

• Develop a study management plan in conjunction with the Director of Clinical Operations, and sponsor representative(s) outlining target KPIs, risk assessment, and contingency planning.

• Lead multidisciplinary Study Management Team.

• End-to-end management of clinical studies to ensure appropriate resourcing and timely and high- quality delivery by all functional areas. Ability to identify and organize resources and services needed to accomplish tasks, set objectives, plan for contingencies, and managing time effect.

• Assist in screening, selection, and management vendors in accordance with contractual timelines, sponsor specifications, quality, budget, and GCP.

• Develop and monitor study metrics to continuously assess study progress.

• Act as the primary point of contact between and sponsor project team. Protocol Preparation & Review

• Reviews and comprehends the protocol.

• Attends investigator meetings as required or requested by the PI.

• Collaborates with the PI to prepare IRB/HRPO and any other regulatory submission documents as required by the protocol.

• Prepares other study materials as requested by the PI. These study materials include, but are not limited to, the informed consent document; case report forms (CRFs), and enrollment logs.

• Establishes and organizes study files, including but not limited to, regulatory binders, study specific source documentation and other materials.

Conduct of Research

• Reviews and develops a familiarity with the protocol, e.g., study proceedings and timelines, inclusion and exclusion criteria, confidentiality, privacy protections.

• Assists PI in communication of study requirements to all individuals involved in the study. Provides appropriate training and tools for study team members. Documents date of training and signatures of study personnel trained on study specific training log.

• Collects documents needed for HHCP to initiate the study and submit to the sponsor (e.g.,, CVs, etc.).

• Works with the PI to develop and implement recruitment strategies in accordance with HRPO (IRB) requirements and approvals.

• Conducts or participates in the informed consent process including interactions with the HRPO

(IRB) and discussions with research participants, including answering any questions related to the study. Obtains appropriate signatures and dates on forms in appropriate places. Assures that amended consent forms are appropriately implemented and signed.

• Screens subjects for eligibility using protocol specific inclusion and exclusion criteria, documenting each potential participant’s eligibility or exclusion.

• Registers each participant in the billing matrix to ensure billing of study procedures to the appropriate funding source.

• Coordinates participant tests.

• Collects data as required by the protocol. Assures timely completion of Case Report Forms.

• Maintains study timelines. And reports for study

• Maintains adequate inventory of study supplies.

• Retains all study records in accordance with sponsor requirements and University of Miami policies and procedures.

• Maintains effective and ongoing communication with sponsor, research participants and PI during the course of the study.

• Works with the PI to manage the day to day activities of the study including problem solving, communication and protocol management.

• Vendor and Agencies Management

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11741 SW 150th PL Miami FL, 33196

Cell 347-***-**** ************@*****.***

REINA MALCOLM, FOREIGN MD

UNIVERSITY OF MIAMI ( DON SUFFER CLINICAL RESEARCH CENTER)- MIAMI, FL DEPARTMENT OF NEUROLOGY- EPILEPSY

SENIOR CLINICAL RESEARCH MANAGER JUNE 2019- SEPT2020 General Administrative

• Coordinates with Principal Investigator and University of Miami, Neurology Department, and central administration to help ensure that clinical research and related activities are performed in accordance with Federal regulations and University of Miami Centers and sponsoring agency policies and procedures.

• Cooperates with University of Miami compliance and monitoring efforts related to sponsored program administration and reports instances of noncompliance to the appropriate compliance office.

• Coordinates and facilitates monitoring and auditing visits. Notifies appropriate institutional officials of external audits by sponsor.

• Collaborates with PI and institution to respond to any audit findings and implement approved recommendations.

• Cooperates with University of Miami Neurology Department and sponsoring agency compliance and monitoring efforts related to human research participant protection and reports instances of noncompliance to the appropriate compliance office. Protocol Preparation & Review

• Reviews and comprehends the protocol.

• Attends investigator meetings as required or requested by the PI.

• Collaborates with the PI to prepare IRB/HRPO and any other regulatory submission documents as required by the protocol.

• Prepares other study materials as requested by the PI. These study materials include, but are not limited to, the informed consent document; case report forms (CRFs), and enrollment logs.

• Establishes and organizes study files, including but not limited to, regulatory binders, study specific source documentation and other materials. Conduct of Research

• Reviews and develops a familiarity with the protocol, e.g., study proceedings and timelines, inclusion and exclusion criteria, confidentiality, privacy protections.

• Assists PI in communication of study requirements to all individuals involved in the study. Provides appropriate training and tools for study team members. Documents date of training and signatures of study personnel trained on study specific training log.

• Collects documents needed to initiate the study and submit to the sponsor (e.g., W9, CVs, etc.).

• Works with the PI to develop and implement recruitment strategies in accordance with HRPO

(IRB) requirements and approvals.

• Conducts or participates in the informed consent process including interactions with the HRPO

(IRB) and discussions with research participants, including answering any questions related to the study. Obtains appropriate signatures and dates on forms in appropriate places. Assures that amended consent forms are appropriately implemented and signed.

• Screens subjects for eligibility using protocol specific inclusion and exclusion criteria, documenting each potential participant’s eligibility or exclusion.

• Registers each participant in the billing matrix to ensure billing of study procedures to the appropriate funding source.

• Coordinates participant tests.

• Collects data as required by the protocol. Assures timely completion of Case Report Forms.

• Maintains study timelines.

• Maintains adequate inventory of study supplies.

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11741 SW 150th PL Miami FL, 33196

Cell 347-***-**** ************@*****.***

REINA MALCOLM, FOREIGN MD

UNIVERSITY OF MIAMI

DEPARTMENT OF PEDIATRIC

SENIOR CLINICAL RESEARCH MANAGER JANUARY 14, 2019-MAY 31, 2019 General Administrative

• Coordinates with Principal Investigator Pediatric Department, and central administration to help ensure that clinical research and related activities are performed in accordance with Federal regulations and University of Miami Centers and sponsoring agency policies and procedures.

• Cooperates with University of Miami compliance and monitoring efforts related to sponsored program administration and reports instances of noncompliance to the appropriate compliance office.

• Collaborates with PI and Pediatric Department and institution to respond to any audit findings and implement approved recommendations.

• Administration amendments ( Reimbursements and Grants reports)

• Conduct Progress Reports

Protocol Preparation & Review

• Reviews and comprehends the protocol.

• Attends investigator meetings as required or requested by the PI.

• Prepares other study materials as requested by the Pediatric Department. These study materials include, but are not limited to, the informed consent document; case report forms (CRFs), and enrollment logs.

• Establishes and organizes study files, including but not limited to, regulatory binders, study specific source documentation and other materials as need it. Conduct of Clinical Research Trials for Pediatric Department

• Reviews and develops a familiarity with the protocol, e.g., study proceedings and timelines, inclusion and exclusion criteria, confidentiality, privacy protections.

• Assists PI in communication of study requirements to all individuals involved in the study. Provides appropriate training and tools for study team members. Documents date of training and signatures of study personnel trained on study specific training log.

• Works with the PI to develop and implement recruitment strategies in accordance with HRPO

(IRB) requirements and approvals.

• Conducts or participates in the informed consent process including interactions with the HRPO

(IRB) and discussions with research participants, including answering any questions related to the Page 5 of 10

REINA MALCOLM, FOREIGN MD

11741 SW 150th PL Miami FL, 33196

Cell 347-***-**** ************@*****.***

• Completes study documentation and maintains study files in accordance with sponsor requirements and University of Miami policies and procedures including, but not limited to, consent forms, source documentation, case report forms, and investigational material accountability forms.

• Retains all study records in accordance with sponsor requirements and University of Miami policies and procedures.

• Maintains effective and ongoing communication with sponsor, research participants and PI during the course of the study.

• Assists PI in preparation of any modifications to the scientific protocol in accordance with Federal regulations and University of Miami and sponsoring agency policies and procedures.

• Works with the PI to manage the day to day activities of the study including problem solving, communication and protocol management.

CLINICAL TRIAL: A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO INVESTIGATE THE EFFICACY AND SAFETY OF CANNABIDIOL (GWP42003-P; CBD) AS ADJUNCTIVE TREATMENT FOR SEIZURES ASSOCIATED WITH LENNOX-GASTAUT SYNDROME IN CHILDREN AND ADULTS.

Mount Sinai Researchers Identify Brain Mechanism for Resilience in People with High Risk of Bipolar Disorder

Psychotic disorders, like schizophrenia and bipolar disorder, disturb particularly human aspects of perception and cognition. General Administrative

• Coordinates with Principal Investigator Pediatric- Neurology Department, and central administration to help ensure that clinical research and related activities are performed in accordance with Federal regulations and Mount Sinai Beth Israel Hospital Centers and sponsoring agency policies and procedures.

• Cooperates with Mount Sinai Hospital Centers compliance and monitoring efforts related to sponsored program administration and reports instances of noncompliance to the appropriate compliance office.

• Coordinates and facilitates monitoring and auditing visits. Notifies appropriate institutional officials of external audits by sponsor.

• Collaborates with PI and institution to respond to any audit findings and implement approved recommendations.

• Cooperates with Mount Sinai Hospital Centers and sponsoring agency compliance and monitoring efforts related to human research participant protection and reports instances of noncompliance to the appropriate compliance office.

Protocol Preparation & Review

• Reviews and comprehends the protocol.

• Attends investigator meetings as required or requested by the PI.

• Collaborates with the PI to prepare IRB/HRPO and any other regulatory submission documents as required by the protocol.

• Prepares other study materials as requested by the PI. These study materials include, but are not limited to, the informed consent document; case report forms (CRFs), and enrollment logs. REINA MALCOLM, FOREIGN MD

11741 SW 150th PL Miami FL, 33196

Cell 347-***-**** ************@*****.***

study. Obtains appropriate signatures and dates on forms in appropriate places. Assures that amended consent forms are appropriately implemented and signed.

• Help to Screens subjects for eligibility using protocol specific inclusion and exclusion criteria, documenting each potential participant’s eligibility or exclusion.

• Maintains study timelines.

• Completes study documentation and maintains study files in accordance with sponsor requirements and Mount Sinai Beth Israel Hospital policies and procedures including, but not limited to, consent forms, source documentation, case report forms, and investigational material accountability forms.

• Retains all study records in accordance with sponsor requirements and maintains effective and ongoing communication with sponsor, research participants and PI during the course of the study.

• Works with the PI to manage the day to day activities of the study including problem solving, communication and protocol management.

PROFESSIONAL EXPERIENCE

MOUNT SINAI BETH ISRAEL - New York, NY

DEPARTMENT OF NEUROLOGY-PEDIATRIC-EPILEPSY-BIOLAR DISORDER-SCHIZOPHRENIA PEDIATRIC SENIOR CLINICAL RESEARCH MANAGER - AUGUST 2015-2019 Page 6 of 10

11741 SW 150th PL Miami FL, 33196

Cell 347-***-**** ************@*****.***

• Establishes and organizes study files, including but not limited to, regulatory binders, study specific source documentation and other materials.

Conduct of Research

• Reviews and develops a familiarity with the protocol, e.g., study proceedings and timelines, inclusion and exclusion criteria, confidentiality, privacy protections.

• Assists PI in communication of study requirements to all individuals involved in the study. Provides appropriate training and tools for study team members. Documents date of training and signatures of study personnel trained on study specific training log.

• Collects documents needed to initiate the study and submit to the sponsor (e.g., W9, CVs, etc.).

• Works with the PI to develop and implement recruitment strategies in accordance with HRPO

(IRB) requirements and approvals.

• Conducts or participates in the informed consent process including interactions with the HRPO

(IRB) and discussions with research participants, including answering any questions related to the study. Obtains appropriate signatures and dates on forms in appropriate places. Assures that amended consent forms are appropriately implemented and signed.

• Screens subjects for eligibility using protocol specific inclusion and exclusion criteria, documenting each potential participant’s eligibility or exclusion.

• Registers each participant in the billing matrix to ensure billing of study procedures to the appropriate funding source.

• Coordinates participant tests.

• Collects data as required by the protocol. Assures timely completion of Case Report Forms.

• Maintains study timelines.

• Maintains adequate inventory of study supplies.

• Completes study documentation and maintains study files in accordance with sponsor requirements and Mount Sinai Beth Israel Hospital policies and procedures including, but not limited to, consent forms, source documentation, case report forms, and investigational material accountability forms.

• Retains all study records in accordance with sponsor requirements and St. Luke’s Roosevelt Hospital Centers policies and procedures.

• Maintains effective and ongoing communication with sponsor, research participants and PI during the course of the study.

• Assists PI in preparation of any modifications to the scientific protocol in accordance with Federal regulations and Beth Israel Hospital Centers and sponsoring agency policies and procedures.

• Works with the PI to manage the day to day activities of the study including problem solving, communication and protocol management.

MOUNT SINAI ST. LUKE’S ROOSEVELT HOSPITAL - New York, NY DEPARTMENT OF NEUROLOGY- STROKE-PSYCHIATRIC

CLINICAL RESEARCH COORDINATOR - FEB 2012-AUGUST 2015 Clinical Trial: ERICH Ethnic/Racial Variations of Intracerebral Hemorrhage (ERICH) Identify differences in risk factor distribution by race, ethnicity and location of intracerebral hemorrhage

(ICH) using a case-control design. Determine differences in imaging characteristics among AAs and Hispanic ICH Cases compared to Whites using a case-only comparison. Determine differences in outcomes Page 7 of 10

REINA MALCOLM, FOREIGN MD

of ICH based on race/ethnicity compared to non-Hispanic whites using a case-only comparison. Determine level of population admixture between centers, ethnicity and race using a control-only analysis. Clinical Trial: Schizophrenia-Bipolar Disorder: Conducting studies from Phase II-IV for the Psychiatric and Psychology

General Administrative

• Coordinates with Principal Investigator and St. Luke’s Roosevelt Hospital Centers, Neurology Department, and central administration to help ensure that clinical research and related activities are performed in accordance with Federal regulations and St. Luke’s Roosevelt Hospital Centers and sponsoring agency policies and procedures.

• Cooperates with St. Luke’s Roosevelt Hospital Centers compliance and monitoring efforts related to sponsored program administration and reports instances of noncompliance to the appropriate compliance office.

• Coordinates and facilitates monitoring and auditing visits. Notifies appropriate institutional officials of external audits by sponsor.

• Collaborates with PI and institution to respond to any audit findings and implement approved recommendations.

• Cooperates with St. Luke’s Roosevelt Hospital Centers and sponsoring agency compliance and monitoring efforts related to human research participant protection and reports instances of noncompliance to the appropriate compliance office. Protocol Preparation & Review

• Reviews and comprehends the protocol.

• Attends investigator meetings as required or requested by the PI.

• Collaborates with the PI to prepare IRB/HRPO and any other regulatory submission documents as required by the protocol.

• Prepares other study materials as requested by the PI. These study materials include, but are not limited to, the informed consent document; case report forms (CRFs), and enrollment logs.

• Establishes and organizes study files, including but not limited to, regulatory binders, study specific source documentation and other materials.

Conduct of Research

• Reviews and develops a familiarity with the protocol, e.g., study proceedings and timelines, inclusion and exclusion criteria, confidentiality, privacy protections.

• Assists PI in communication of study requirements to all individuals involved in the study. Provides appropriate training and tools for study team members. Documents date of training and signatures of study personnel trained on study specific training log.

• Collects documents needed to initiate the study and submit to the sponsor (e.g., W9, CVs, etc.).

• Works with the PI to develop and implement recruitment strategies in accordance with HRPO (IRB) requirements and approvals.

• Conducts or participates in the informed consent process including interactions with the HRPO

(IRB) and discussions with research participants, including answering any questions related to the study. Obtains appropriate signatures and dates on forms in appropriate places. Assures that amended consent forms are appropriately implemented and signed.

• Screens subjects for eligibility using protocol specific inclusion and exclusion criteria, documenting each potential participant’s eligibility or exclusion.

• Registers each participant in the billing matrix to ensure billing of study procedures to the appropriate funding source.

• Coordinates participant tests.

• Collects data as required by the protocol. Assures timely completion of Case Report Forms.

• Maintains study timelines.

• Maintains adequate inventory of study supplies.

11741 SW 150th PL Miami FL, 33196

Cell 347-***-**** ************@*****.***

REINA MALCOLM, FOREIGN MD

Page 8 of 10

• Completes study documentation and maintains study files in accordance with sponsor requirements and St. Luke’s Roosevelt Hospital Centers policies and procedures including, but not limited to, consent forms, source documentation, case report forms, and investigational material accountability forms.

• Retains all study records in accordance with sponsor requirements and St. Luke’s Roosevelt Hospital Centers policies and procedures.

• Maintains effective and ongoing communication with sponsor, research participants and PI during the course of the study.

• Assists PI in preparation of any modifications to the scientific protocol in accordance with Federal regulations and St. Luke’s Roosevelt Hospital Centers and sponsoring agency policies and procedures.

• Works with the PI to manage the day-to-day activities of the study including problem solving, communication and protocol management.

COLUMBIA-PRESBYTERIAN MEDICAL CENTER - New York, NY DEPARTMENT OF

CLINICAL RESEARCH COORDINATOR - 2011-FEB 2012

Clinical Trial: Multi-Ethnic Study of Atherosclerosis (MESA) MESA is a longitudinal study of the characteristics of subclinical cardiovascular disease (disease detected non-invasively before it has produced clinical signs and symptoms) and risk factors that predict progression from subclinical to clinically cardiovascular disease, in a diverse population-based sample of 6,814 men and women aged 45-84.

Patient Identification

o Identify possible candidates for protocols by maintaining a high profile as the contact for information regarding clinical trial protocols

o Communicating directly with the PI, co-investigators, and other consult services at the institution o Educate potential patient/subjects on clinical trial protocols Protocol Eligibility

o Confirmation of patient eligibility for protocol and determining eligibility as specified by the protocol

o Review the patient’s medical records

o Assure that pre-study evaluations have been completed within the time specified in the study parameters of the protocol

o Inform the investigators of any required studies that must be ordered to comply with the study parameters

o Complete the eligibility checklist

o Ensure that informed consent has been obtained in compliance with federal, state, and IRB guidelines, as well as HIPAA authorization

o Ensure and document that the patient has given informed consent before administering any study-related tests, treatments, procedures, and/or questionnaires Patient/Subject Management

o Coordinate care of patient/subject

o Develop recruitment plan in collaboration with clinical teams o Review protocols to determine recruitment needs

o Identifies patient profiles, patient dynamics, potential recruitment barriers o Administered EKG, Phlebotomy, Anthropometry Test, Elasticity Test o Collected vitals (BP, Oximetry)

o Performed DLCO Pulmonary Test

o Administered Cognitive Neurology Test

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11741 SW 150th PL Miami FL, 33196

Cell 347-***-**** ************@*****.***

REINA MALCOLM, FOREIGN MD

11741 SW 150th PL Miami FL, 33196

Cell 347-***-**** ************@*****.***

Pontificia Universidad Catolica Madre y Maestra(PUCMM) Efectividad del Tinidazol vs Albendazole n el tratamiento de la Giardiasis Intestinal en Ninos de 2-10 anos Diagnosticados por Aspirado de Jugo Gastrico en el Centro Medico Cibao Santiago( Marzo- Agosto 1999) Pontificia Universidad Catolica Madre y Maestra (PUCMM) Behavioral Research Dominican Republic, 2001-2003.

TECHNICAL SKILLS

Software:

• Microsoft Word • Microsoft Excel • Microsoft Power Point

• Microsoft Outlook • EMSTAT • PACS

• PRISM • NCBI: PubMed • IQ Registry

• Inmedidata -Rave

COURSES

Genes and the Human Condition (From Behavior to Biotechnology): University of Maryland, College Park.(Coursera)

Medical Neuroscience: Duke University (Coursera)

Nutrition for Health Promotion and Disease Prevention (Coursera) EDUCATION/CERTIFICATIONS

DOCTOR IN MEDICINE, MD

Pontificia Universidad Catolica Madre y Maestra

Dominican Republic, 2000

CITI Training Certifications

RAVE EDC Certifications (2016)

AHA Certification in NIH Stroke Scale, 2012

Blood borne Pathogen Training,

Phlebotomy Certification,

EKG Certification,

AFFILIATIONS

American Heart-Stroke Society

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REINA MALCOLM, FOREIGN MD

Contact this candidate