CrawlJobs Logo

Medical Team Associate

childrenshospital.org Logo

Boston Children's Hospital

Location Icon

Location:
United States , Boston

Category Icon

Job Type Icon

Contract Type:
Not provided

Salary Icon

Salary:

44657.60 - 69773.60 USD / Year

Job Description:

The Medical Team Associate supports resident physician providers by coordinating non-clinical inpatient care, which enhances hospital efficiency and improves bed utilization through facilitating early morning discharges. They also coordinate inpatient activities during and after rounds according to approved hospital policies, functioning as an essential team member under the Pediatric Hospital Medicine Division and the Boston Combined Residency Program.

Job Responsibility:

  • Facilitating coordination and communication among team members and scheduling related activities, such as rounds and interpreter services
  • Managing and implementing patient care plans and ensuring patient records and data are obtained for effective care
  • Scheduling inpatient and outpatient tests and consultations based on care plans discussed during rounds
  • Confirming outpatient prescriptions with pharmacies and managing requests for computer and phone service support
  • Coordinating meetings for families and care teams, participating in quality improvement efforts, and collaborating with the care team.

Requirements:

  • High School diploma required
  • Bachelor’s degree in Science preferred
  • A minimum of one year of experience in a related role is preferred
  • Proficiency in use of Microsoft Windows and Office and ability to train in and use various aspects of the electronic medical record, including PowerChart and Patient Inquiry
  • Strong attention to detail, with ability to function proactively and anticipate needs of physicians and/or patients
  • Ability to establish and maintain effective working relationships with residents and the rest of the inter-professional team
  • Advanced communication skills in order to persuade and negotiate with others on important matters
  • Strong interpersonal skills, with an ability to effectively balance diverse skill sets and perspectives
  • Ability to multi-task, prioritize tasks and manage time efficiently and effectively
  • Compliance with all national and hospital regulatory guidelines such as HIPAA requirements, and the highest ethical standards, particularly related to integrity, honesty and confidentiality.
What we offer:
  • flexible schedules
  • affordable health, vision and dental insurance
  • child care and student loan subsidies
  • generous levels of time off
  • 403(b) Retirement Savings plan
  • Pension
  • Tuition and certain License and Certification Reimbursement
  • cell phone plan discounts
  • discounted rates on T-passes

Additional Information:

Job Posted:
March 21, 2026

Employment Type:
Fulltime
Work Type:
On-site work
Job Link Share:

Looking for more opportunities? Search for other job offers that match your skills and interests.

Briefcase Icon

Similar Jobs for Medical Team Associate

Associate Medical Director, Pediatrics

Provide medical leadership in pediatrics and collaborative clinical support to a...
Location
Location
United States
Salary
Salary:
180000.00 - 200000.00 USD / Year
pomelocare.com Logo
Pomelo Care
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Medical degree from an accredited US medical school
  • Successful completion of an accredited US residency program in a directly related field (Pediatrics or Family Medicine with substantial experience with pediatrics)
  • A minimum of three years of post-residency experience in pediatric primary care and/or pediatric urgent care
  • Active, unrestricted license to practice in any US state and willingness to obtain licenses in all US states via the Interstate Medical Licensure Compact
  • Experience leading successful teams, with track record of outstanding collaboration and teamwork
  • A sense of urgency to improve clinical outcomes coupled with exceptional organization and attention to detail
  • A growth mindset with the ability to approach process change and ambiguous situations with enthusiasm, creativity, and accountability
  • Facility using multiple tech platforms, with an eagerness for advising about platform improvements and adapting to new systems
  • Eager to thrive in a fast-paced, metric-driven environment
  • Phenomenal interpersonal and communication skills
Job Responsibility
Job Responsibility
  • Provide collaborative physician supervision and consultation for an experienced team of APPs, nursing leadership, and RNs in the field of pediatrics including conducting quality assurance review for Pediatric APPs
  • Serve as the pediatric medical director in regional cross-disciplinary team-based care coordination meetings and work with in-house clinical specialties to develop holistic individualized care plans
  • Own clinical content development for our Pediatrics program, serving as the subject matter expert across internal clinician-facing protocols and patient-facing content
  • Support the recruitment and training of pediatric medical providers
  • Help drive our population health programs toward healthier outcomes by partnering closely with Market Operations leads and OB Regional Medical Director to identify gaps and improvement opportunities
  • Identify and implement interventions to address cross-disciplinary or practice performance improvement needs
  • Facilitate and lead cross-disciplinary review sessions for episodic events and pediatric case reviews
  • Engage directly in patient care as a Pomelo provider
  • Actively participate in on-call schedules including overnights, weekends, and holidays
What we offer
What we offer
  • Competitive healthcare benefits
  • Generous equity compensation
  • Generous PTO policy
  • Fulltime
Read More
Arrow Right

Physician Associate Medical Director

Harrison's Hope Hospice is seeking a (Contract) PRN Physician Associate Medical ...
Location
Location
United States , Meridian
Salary
Salary:
Not provided
arcadiahomecare.com Logo
Arcadia Home Care and Staffing - an Addus family company
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Graduate of an accredited school of medicine with a current license as a Doctor of Medicine or Osteopathy in the state(s) of practice
  • Must have at least one year of demonstrated work experience in hospice or in another setting managing the care of terminally ill patients
  • Understands hospice philosophy, issues of death/dying, and palliative care principles
  • Must have admission privileges at one or more hospitals in the hospice's geographical service area
  • Must be a licensed driver with an automobile that is insured in accordance with state and/or organization requirements and is in good working order
  • Demonstrates excellent observation, problem solving, verbal and written communications
  • Shows ability to organize and prioritize workload independently
  • This position requires a minimum of 8 education hours
Job Responsibility
Job Responsibility
  • Certifies and recertifies patients' medical eligibility for hospice services in accordance with hospice program policy and Local Clinical Determination guidelines
  • Attends all Interdisciplinary Group Meetings as the physician team member
  • Provides Face to Face medical assessment of patient's eligibility for continued admission as required by CFR Section 1306.11 when requested by the hospice team
  • Provides such care to hospice patients in their personal residence, skilled nursing facility, assisted living facility or local hospital
  • Documents initial certifications, re-certifications, physician orders, and face to face assessments in a timely and complete manner utilizing the appropriate format to ensure regulatory compliance
  • Demonstrates exceptional service to patients, families, referral sources, co-workers, and other customers
Read More
Arrow Right

Associate Medical Director

Associate Medical Director, Oncology. ICON plc is a world-leading healthcare int...
Location
Location
Poland , Warsaw
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Medical degree (MD) required
  • Board certification preferred in oncology/haematology
  • Minimum of 3 years of experience in clinical research or medical affairs within the pharmaceutical or biotechnology industry
  • Strong understanding of clinical trial design, execution, and regulatory requirements
  • Experience in immune oncology
  • Excellent communication and relational skills
  • Demonstrated leadership and problem-solving abilities
Job Responsibility
Job Responsibility
  • Collaborating with cross-functional teams to design clinical development plans and study protocols
  • Providing medical oversight and guidance throughout the lifecycle of clinical trials
  • Ongoing medical review of data, supporting Safety Review Committees
  • Interpreting complex medical and clinical trial data to support decision-making and regulatory submissions
  • Contributing to the development of scientific publications, presentations, and regulatory documents
  • Building and maintaining relationships with investigators, key opinion leaders and regulatory authorities
What we offer
What we offer
  • Various annual leave entitlements
  • A range of health insurance offerings
  • Competitive retirement planning offerings
  • Global Employee Assistance Programme, LifeWorks
  • Life assurance
  • Flexible country-specific optional benefits
Read More
Arrow Right

Associate Medical Director of PACE

Join HopeWest, a non-profit healthcare organization, as their next Associate Med...
Location
Location
United States , Grand Junction
Salary
Salary:
212000.00 - 234000.00 USD / Year
besmith.com Logo
B.E. Smith
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • MD/DO is required
  • A minimum of five years of clinical experience is required
  • A minimum of five years of supervisory experience is strongly preferred
  • Previous PACE experience is strongly preferred
  • Controlled substance license with current DEA license number
  • Eligible or currently possess a Medicare/Medicaid NPI number
Job Responsibility
Job Responsibility
  • Lead clinical operations for approximately 222+ PACE participants, overseeing their primary care needs and acts as the expert in their medical care
  • Help to oversee a team of Nurse Practitioners and will work in collaboration with RNs, CNAs, PT/OT, Managers, and IDT
  • Focus on ongoing clinical initiatives including care plans, behavioral health initiatives, and case reviews
  • Foster trust through strong staff relationships, assess team dynamics, identify and remove barriers, leverage data to drive decisions, and provide recommendations for improvement and positive change
  • Clinical oversight related to workflow development, fall risks, committee reviews, finances/invoices and some pharmacy workflows
What we offer
What we offer
  • Health insurance coverage
  • Retirement benefits
  • Bonuses
  • Fulltime
Read More
Arrow Right

Medical Research Associate

Medical Research Associate (Phlebotomist/Medical Assistant)- ICON San Antonio TX...
Location
Location
United States , San Antonio
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • High School Diploma or equivalency with medical assistant training/certification or other allied health certification
  • Medical Assistant, Phlebotomy Technician, Paramedic, EMT, OR LVN preferably with two years of experience
  • Strong organizational and time management skills, with attention to detail in data collection and documentation
  • Proficiency with research software and tools for data entry, analysis, and reporting
  • Excellent communication and teamwork skills, with the ability to work collaboratively with researchers and other stakeholders
Job Responsibility
Job Responsibility
  • Assisting in the planning and execution of clinical trials and research studies, including data collection and management
  • Supporting the research team with literature reviews, data entry, and analysis to inform study protocols and findings
  • Maintaining accurate and organized research documentation, ensuring compliance with regulatory and ethical standards
  • Collaborating with cross-functional teams to ensure timely completion of research tasks and adherence to study timelines
  • Assisting with the preparation of research reports, manuscripts, and presentations for internal and external stakeholders
What we offer
What we offer
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others
  • Parttime
Read More
Arrow Right

Associate Director / Director, Medical Writing

Beam is seeking a highly talented and motivated AD/Director to join our growing ...
Location
Location
United States , Cambridge
Salary
Salary:
180000.00 - 260000.00 USD / Year
beamtx.com Logo
Beam Therapeutics
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree required
  • MS, PharmD, or PhD preferred in a life science or health discipline
  • 12+ years of clinical/regulatory medical writing experience in the pharmaceutical or biotech industry
  • A solid understanding of ICH guidelines, GxP, and relevant regulatory requirements
  • Demonstrated understanding of clinical regulatory documents (ie, protocol, IB, CSR, summaries for product filing, etc.) and experience as a lead author with such documents
  • Excellent communication skills, both oral and written
  • Ability to build strong relationships and work collaboratively across functions
  • Effective organizational and meeting skills and attention to detail
  • Experience with workflow management within standard document management systems
  • Ability to come onsite when needed such as for important meetings and team/company functions
Job Responsibility
Job Responsibility
  • Act as lead writer for clinical regulatory documents for the hematology program
  • Plan and lead the development of clinical study documents, working with cross-functional colleagues
  • Work closely with the regulatory team and other writers on regulatory document submissions
  • Assist with developing and maintaining medical writing process documents
  • Assist with evaluation and interpretation of the medical literature across several domains, such as study design, clinical development planning, statistical meaningfulness, and scientific rigor
  • Contribute to statistical output plans concerning organization and table layout for specific documents
  • Project management, strategic design, planning, team input, and reviews
  • Opportunities for management/mentorship of other writers
  • Fulltime
Read More
Arrow Right

Regional Medical Advisor Manager - Migraine

Maximize the value of Pfizer products to Chinese patients and health care profes...
Location
Location
China , Beijing
Salary
Salary:
Not provided
pfizer.de Logo
Pfizer
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Master degree major in clinical medicine, Medical doctoral degree or PHD in medical is preferred
  • Master of Business Administration is a plus
  • 3 years clinical practice in Tier 3 hospitals (corresponding specialty is preferred)
  • MD or PHD with 3+ years medical affairs experience in multinational pharmaceutical companies experience, or Master with 5+ years’ experience
  • Therapeutic area knowledge: familiar with the disease knowledge and clinical practice of the therapeutic area
  • Language: Proficiency in oral and written English
  • Good understanding about pharmaceutical business
  • In-depth Clinical trial knowledge
  • Computer: Good at Microsoft Office software
  • Strong business acumen with farsighted view
Job Responsibility
Job Responsibility
  • Maximize the value of Pfizer products to Chinese patients and health care professional within Pfizer’s vision and mission
  • Responsible for promoting strategic collaboration and implementation of regional medical affairs with the government, academic associates and medical institutions and exploring innovative chronic disease management models in the new environment, graded diagnosis and treatment models, efficient doctor education models, and patient-centered disease management models
  • Develop promoting strategy from field based medical perspective to maximize products and medical value and long term development
  • Develop effective medical plan for the defined portfolio therapeutic area(s) aligning with products development strategy, maximize the value of field based medical and ensure its timely execution
  • Identify medical opportunity in collaboration with government, academic associations and medical institutions for business initiative and decisions
  • Exploring innovative chronic disease management models, diagnosis and treatment models to adapt to new environments and challenges
  • Develop and execute publication plan, provide input to the publication plan, provide ideas for generating manuscripts of scientific interest, and actively review manuscripts and abstracts to ensure medical and scientific accuracy
  • Work with BU sale leaders on portfolio therapeutic strategies and key issues resolution from medical point of view
  • Synergy available resources internally and externally to promote the development and execution of field based medical team
  • Develop sale team medical capability through medical training ,lecture delivery and medical knowledge update through various channel
  • Fulltime
Read More
Arrow Right

Field Service Associate

The ideal candidate for our Field Service Associate position is an individual wh...
Location
Location
Salary
Salary:
50000.00 - 70000.00 USD / Year
canfieldsci.com Logo
canfield scientific
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Associate’s degree or equivalent and minimum 3 years in a professional corporate setting
  • Proficiency with Microsoft Office
  • Willingness to travel up to 40-50%, at times on short notice, with the ability to lift, move, and carry equipment up to 50 lbs regularly
  • Adaptability and problem-solving skills to troubleshoot issues in a fast-paced environment as well as provide guidance on how to best leverage software tools
  • Experienced with utilizing all aspects of computer technology as well as utilizing basic hardware tools
  • Strong time management, organizational, and critical thinking skills in order to meet deadlines, willingness to learn, and adhere to travel and training schedules
Job Responsibility
Job Responsibility
  • Coordinate and deliver online and onsite hands-on product training for clients ranging from 2-4 hours
  • Perform onsite installations of photographic hardware equipment and Canfield computer software
  • Assist technical support teams and distributor partner field teams with troubleshooting regarding installation, operation, and calibration of medical photography systems and software
  • Post-sale customer account management, including scheduling additional trainings and periodic check-ins
  • Provide feedback to product management and development teams continually
  • Document customer activity and training notes in thorough service reports
What we offer
What we offer
  • paid days off
  • medical, dental, and vision insurance
  • may be eligible for a discretionary bonus
  • a 401(k) plan with employer match (currently set at 50%)
  • Fulltime
Read More
Arrow Right