Physician Relations Director jobs in Maryland

Physician Relations Director directs and oversees programs designed to foster positive relations between physicians and the hospital or healthcare facility. Promotes the organization among members of the medical community in order to establish partnerships and affiliations. Being a Physician Relations Director requires a bachelor's degree in area of specialty. Typically reports to top management. The Physician Relations Director manages a departmental sub-function within a broader departmental function. Creates functional strategies and specific objectives for the sub-function and develops budgets/policies/procedures to support the functional infrastructure. Deep knowledge of the managed sub-function and solid knowledge of the overall departmental function. To be a Physician Relations Director typically requires 5+ years of managerial experience. (Copyright 2024 Salary.com)

1
Global Clinical Program Lead (Physician), Late Respiratory Dev
  • 10001001 - Director Physician
  • Gaithersburg, MD FULL_TIME
  • Job Title: Global Clinical Program Lead (Physician), Late Respiratory R&D

    Location: In office with Flexibility in Gaithersburg MD

    Make a more meaningful contribution by impacting patients’ lives every day.

    Contribute to our growing pipeline. Join a place with the commitment, knowledge and backing from the business to continue expanding our pipeline. With one of the broadest and deepest pipelines, we are determined to keep contributing and pushing forward. When we get it right there’s nothing more motivating.
     

    AZ’s vision is to grow and expand the indications and assets in respiratory and or immunology to become a major player in the field.

    This Global Clinical Program Lead (GCPL) role in Late stage clinical development in R&I is designed to help deliver on that ambition.

    What you will do:

    GCPL is responsible for the design, conduct, monitoring, data interpretation and reporting of immunology clinical trials within the program to ensure clinical data collected allow to assess the benefits and risks of the compound, as aligned with overall clinical development program strategy globally, including indications. The GCPL will ensure studies are operated according to the highest scientific and ethical standards and in compliance with internal SOPs, local regulations, GCP and regulatory requirements.

    The GCPL will be able to deputize for Global Clinical Head (GCH) and lead independently on development activities of the clinical development plan.

    Typical Accountabilities:

    • Is responsible for study design concept delivery

    • Is responsible for driving clinical and scientific decisions within Global Study Team remits together with other team members

    • Is accountable for clinical, scientific, and ethical components of studies including patient safety on a study and/or program level in compliance with Good Clinical Practice

    • Is accountable for scientific medical input to all relevant study documents (including and not limited to protocol, statistical analysis plan, amendments, informed consent, case report forms, safety, and risk-based monitoring plans) to ensure consistency within clinical program and alignment with scientific rationale.

    • Is accountable for scientific medical content at international investigator meetings, and support to local Marketing Companies (MC) for country level activities

    • Is accountable for safety surveillance on a study level and/or program level including the process for Adverse Events (AE)/ Serious AE reporting.

    • Reviews (with the GCH) the Clinical Study Report and plays key role in preparation and production of relevant sections (Introduction, Results, Discussion).

    • Is accountable for induction and education of new Global Study Team members. May also contribute to clinical trial improvement workstreams on behalf of the Clinical function.

    • May be accountable to GCH (or delegate) and TA leadership for identifying risks and proposing mitigation strategies to deliver successful phase IIb, III, IV or Life Cycle Management studies

    • Delivery of clinical, scientific, and medical information/query responses to Regulatory Agencies, Ethic Committees, Marketing Companies (MCs), and investigators/sites, and provides clarifications as well as solves clinical, scientific, and medical issues in the Global Study Team

    • Clinical representative on indication in Global and Clinical Product Teams and/or sub-teams

    • Leads governance interactions in conjunction with or as delegated by the GCH such as DRACs, DRCs, PRCs

    • Co-leads the study and program strategy for publication development and approval of publications with the GCH

    • Line management of project study physicians and scientists


    Regulatory Interactions: 

    • Plays key role in development of the clinical sections of regulatory submission documents and is accountable to GCH for their content

    • Provides a leadership role in writing responses to comments/questions of Regulatory Authorities for clinical modules

    • Leads as delegated by GCH the strategy for the development of regulatory agency briefing documents (BD) and ensure BD completeness; defend BD positions during regulatory meetings as delegated by GCH


    Scientific Medical & Analytical Accountabilities:

    • Stays up to date with relevant scientific literature, and can message key impactful points, as applicable

    • Delivers analyses of clinical data in a balanced, statistically sound fashion, to drive interpretations and further idea generation

    • Scientific/medical expertise for the Product Team, in analyses and interpretation of trial data.

    Messaging and external impact accountabilities

    • Maintains high degree of understanding and awareness on new and emerging medical development advances in the relevant therapeutic area globally.

    • Builds trustworthy relationships with steering committees/executive committees, academic research organizations and clinical research organizations as applicable

    • Works with international colleagues and with external Alliance partners on development initiatives and regulatory issues

    • Provides guidance for externally sponsored trials in cooperation with regional MCs


    People Management:

    • 5-8 direct reports

    Essential Education, Skills and Experience Required for this Role:

    • Medical degree (e.g. MD, with specialist training or significant experience in either allergy/immunology/autoimmune diseases and  extensive experience from clinical development in pharmaceutical industry

    • Experience in matrix team environment with interplay between clinical, commercial, drug safety and regulatory

    • Minimum of 5 yrs and ideally more than 8 yrs experience in pharma industry, with experience in leading late phase clinical trials to support approval

    • Knowledge of biostatistics, global regulatory environment, and pharmacovigilance relevant to the role

    • Experience in leading a clinical program to support an indication: design, clinical development plan and Target Product Profile

    • Experience in writing clinical aspects of briefing documents for regulatory interactions

    • Plays a critical role in writing sections of a submission dossier

    • Good presentation skills and effective communication with internal and external collaborators

    • Knowledge and experience working across projects, with a fast-learning curve when moving into new disease areas

    • Line management experience

     

    Behaviors Required of this Role:

    • Demonstrated leadership qualities with focus on collaborative working skills, trust, and openness, irrespective of cultural setting

    • Proven teamwork and collaboration skills

    • Demonstrates AstraZeneca Values and Behaviors

    AstraZeneca an Employer of Choice:

    AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be! AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law. AstraZeneca only employs individuals with the right to work in the country/ies where the role is advertised.

    We offer a competitive Total Reward program including a market driven base salary, bonus and long term incentive. We also provide a generous paid time off program and a comprehensive benefits package!  If you have what it takes to create a culture of courageous leadership, creativity and collaboration, please apply today!

    When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working give us the platform we need to connect, work at pace and challenge perceptions. That’s why we work, on average, a minimum of four days per week from the office. But that doesn’t mean we’re not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. 

    AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.

    AstraZeneca requires all US employees to be fully vaccinated for COVID-19 but will consider requests for reasonable accommodations as required by applicable law.

  • 10 Days Ago

1
Senior Medical Director, Early R&I, Rheumatology/Immunology
  • 10001001 - Director Physician
  • Gaithersburg, MD FULL_TIME
  • Job Title - Senior Medical Director, Early Clinical Research, Rheumatology/Clinical ImmunologyLocation - Office based role in Gaithersburg MD OR Boston MA OR Barcelona Spain OR Gothenburg Sweden - (al...
  • 7 Days Ago

U
Director, Corporate and Foundation Relations
  • USNA Alumni Association & Foundation
  • Annapolis, MD FULL_TIME
  • The United States Naval Academy Alumni Association and Foundation in Annapolis, Maryland is looking to hire a full-time Director, Corporate and Foundation Relations to join the Donor Engagement & Stra...
  • 14 Days Ago

M
DIRECTOR HUMAN RELATIONS (HYBRID)
  • mccormickt3.valhalla.stage
  • HUNT VALLEY, MD FULL_TIME
  • You may know McCormick as a leader in herbs, spices, seasonings, and condiments – and we’re only getting started. At McCormick, we’re always looking for new people to bring their unique flavor to our ...
  • Just Posted

R
Associate Director, Investor Relations
  • Regenxbio
  • Rockville, MD FULL_TIME
  • Who we areREGENXBIO is an exceptional place to work. You'll have the opportunity to collaborate with some of the best and the brightest people, touch amazing science, and be a part of extraordinary pl...
  • Just Posted

C
Director of Public Relations
  • CommuniCare Family of Companies
  • Hagerstown, MD FULL_TIME
  • Hagerstown Healthcare Center, a member of the CommuniCare Health Services, is seeking an experienced health care professional with sales and marketing abilities for the position of Director of Public ...
  • 2 Days Ago

C
Medical Doctor
  • Center For New Medicine & Cancer Center for Healing
  • Irvine, CA
  • The Center For New Medicine and Cancer Center For Healing, located in (Irvine) Southern California, is expanding and in ...
  • 4/18/2024 12:00:00 AM

P
Medical Doctor
  • Pivotal Placement Services, Inc
  • Atlanta, GA
  • Would you be willing to serve your local community? At our clinic, we provide the most thorough care for our patients. W...
  • 4/18/2024 12:00:00 AM

H
Medical Doctor -Physician
  • HireTalent - Diversity Staffing & Recruiting Firm
  • Anderson, SC
  • Are you a passionate and experienced Primary Care Physician seeking a challenging yet rewarding opportunity? Look no fur...
  • 4/17/2024 12:00:00 AM

N
Medical Doctor
  • Next Level Medical
  • San Antonio, TX
  • Job Title: Physician Department: Clinical Reports To: Regional Vice President FLSA Status: Exempt Job Summary Provides p...
  • 4/17/2024 12:00:00 AM

1
Urgent Care Physician - Doctor of Medicine/Doctor of Osteopathic
  • 1973
  • Los Angeles, CA
  • Job Description Job Description We are looking to hire a part time physician with either a Doctor of Medicine License or...
  • 4/17/2024 12:00:00 AM

C
Medical Doctor
  • Center For New Medicine & Cancer Center For Healing
  • Irvine, CA
  • The Center For New Medicine and Cancer Center For Healing, located in (Irvine) Southern California, is expanding and in ...
  • 4/16/2024 12:00:00 AM

P
Medical Doctor
  • Pivotal Placement Services Inc
  • Atlanta, GA
  • Would you be willing to serve your local community? At our clinic, we provide the most thorough care for our patients. W...
  • 4/16/2024 12:00:00 AM

A
Medical Doctor
  • Associatesmd Medical Group
  • Hollywood, FL
  • General Summary of Duties: Responsible for providing consultative Non-Invasive General Cardiology medical services withi...
  • 4/16/2024 12:00:00 AM

Maryland (US: /ˈmɛrələnd/ (listen) MERR-əl-ənd) is a state in the Mid-Atlantic region of the United States, bordering Virginia, West Virginia, and the District of Columbia to its south and west; Pennsylvania to its north; and Delaware to its east. The state's largest city is Baltimore, and its capital is Annapolis. Among its occasional nicknames are Old Line State, the Free State, and the Chesapeake Bay State. It is named after the English queen Henrietta Maria, known in England as Queen Mary. Sixteen of Maryland's twenty-three counties border the tidal waters of the Chesapeake Bay estuary and...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Physician Relations Director jobs
$126,610 to $219,909

Physician Relations Director in Augusta, GA
Reporting to the VP of Sales, the Physician Relations Manager will establish relationships with physicians to build referral relationships.
February 13, 2020
Physician Relations Director in Casper, WY
Training and building a successful physician relations marketing program can prove to be challenging for physicians or clinical managers.
December 03, 2019
Physician Relations Director in Rock Island, IL
The Physician Relations Manager (PRM) will be very familiar with hospital operations, language, and roles within the organization and the community.
December 30, 2019