clinical research coordinator Jobs in Boston

clinical research coordinator

clinical research coordinator i Jobs in Boston

clinical research coordinator i

clinic/practice assistant ii Jobs in Boston

clinic/practice assistant ii

clinical research coordinator ii Jobs in Boston

clinical research coordinator ii

administrative coordinator Jobs in Boston

administrative coordinator

patient coordinator group practice school of dental medicine clinical affairs

Boston University

<div><div><div>Change the hiring manager to Katie Briggs
<p>
For the job description: A Patient Coordinator administers the daily desk operations to ensure excellent customer service and front-end operations in the Specialty clinics for both patients and students while meeting educational and fiscal goals. This position strives to make each phase of treatment a very positive experience for all patients from the initial phone call on through the delivery of care to completion. Answer all incoming calls and direct as needed. Check messages and return calls. Greet all scheduled patients, checking them in as arrivals and notifying their doctors. Actively listens in the details of a patient complaint, provides feedback, recommends solutions, and reaches out to supervisors in an effort to resolve issues as needed. Scheduling appointments ensuring continuity of care. Assisting patients with coordination of department referrals. Answering treatment/billing/benefit questions. Triage emergency patients. Provides support to each student with their patient care management issues allowing them to devote their time to the delivery of patient care. Responsible to carry out the established business practices and policies and procedures set forth by the Henry M. Goldman School of Dental Medicine.</p></div></div><p></p><div><br>
<div>
</div></div><br>
<br>
Required Skills<br>
<ul><li>High School Diploma required; Associates degree preferred. events.</li>
<li>Must have previous experience (1-3 years) working in a customer service environment with heavy customer/patient interaction; prior experience in healthcare private practice office, hospital, clinic or dental practice - preferred.</li>
<li>Must have the ability to be flexible and adapt to changes in the work environment including delays and unexpected events.</li></ul><br>
<p></p>
<p>
Skills:</p>
<ul>
<li>Demonstrated ability to establish priorities, meet deadlines, and manage competing demands.</li>
<li>Ability to identify problems/issues, critically thinking through problems (gather and anaylyze information skillfully) and presenting potential solutions in a timely manner.</li>
<li>Ability to maintain confidentiality, remain open to others' ideas with willingness to try new things.</li>
<li>Must be able to successfully collaborate and work in a team environment while also being an individual contributer.</li>
<li>Excellent time management and organizational skills demonstrating the ability of accuracy and thoroughness; monitor own work to ensure quality; ability to multi-taski with the ability to work under pressure, maintain composure and meet deadlines.</li>
<li> Must have strong interpersonal skills that includes strong verbal communication skills with the ability to demonstrate courtesy, respect and professionalism at all times to patients, students, staff and faculty.</li>
<li>Must be adept and comfortable working in a systems driven environment.</li>
<li>Able to adapt to changes in the work environment, manage competing demands and is able to deal with frequent change, delays, or unexpected Consistently at work and on time, follows instructions, respond to management direction and solicits feedback to improve performance.</li></ul><p></p><div><br>
</div>
<div><p><i>We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, natural or protective hairstyle, religion, sex, age, national origin, physical or mental disability, sexual orientation, gender identity, genetic information, military service, pregnancy or pregnancy-related condition, or because of marital, parental, or veteran status. We are a VEVRAA Federal Contractor.</i></p></div></div>

PATIENT COORDINATOR, GROUP PRACTICE, School of Dental Medicine Clinical Affairs

<div><div><div>A Patient Coordinator administers the daily desk operations to ensure excellent customer service and front-end operations in the Specialty clinics for both patients and students while meeting educational and fiscal goals. This position strives to make each phase of treatment a very positive experience for all patients from the initial phone call on through the delivery of care to completion. Answer all incoming calls and direct as needed. Check messages and return calls. Greet all scheduled patients, checking them in as arrivals and notifying their doctors. Actively listens in the details of a patient complaint, provides feedback, recommends solutions, and reaches out to supervisors in an effort to resolve issues as needed. Scheduling appointments ensuring continuity of care. Assisting patients with coordination of department referrals. Answering treatment/billing/benefit questions. Triage emergency patients. Provides support to each student with their patient care management issues allowing them to devote their time to the delivery of patient care. Responsible to carry out the established business practices and policies and procedures set forth by the Henry M. Goldman School of Dental Medicine.</div></div><p></p><div><br>
<div>
</div></div><br>
<br>
Required Skills<br>
<ul><li>High School Diploma required; Associates degree preferred. events.</li>
<li>Must have previous experience (1-3 years) working in a customer service environment with heavy customer/patient interaction; prior experience in healthcare private practice office, hospital, clinic or dental practice - preferred.</li>
<li>Must have the ability to be flexible and adapt to changes in the work environment including delays and unexpected events</li></ul><br>
<p></p>
<p>
Skills:</p>
<ul>
<li>Demonstrated ability to establish priorities, meet deadlines, and manage competing demands.</li>
<li>Ability to identify problems/issues, critically thinking through problems (gather and anaylyze information skillfully) and presenting potential solutions in a timely manner.</li>
<li>Ability to maintain confidentiality, remain open to others' ideas with willingness to try new things.</li>
<li>Must be able to successfully collaborate and work in a team environment while also being an individual contributer.</li>
<li>Excellent time management and organizational skills demonstrating the ability of accuracy and thoroughness; monitor own work to ensure quality; ability to multi-taski with the ability to work under pressure, maintain composure and meet deadlines.</li>
<li>Must have strong interpersonal skills that includes strong verbal communication skills with the ability to demonstrate courtesy, respect and professionalism at all times to patients, students, staff and faculty.</li>
<li>Must be adept and comfortable working in a systems driven environment.</li>
<li>Able to adapt to changes in the work environment, manage competing demands and is able to deal with frequent change, delays, or unexpected Consistently at work and on time, follows instructions, respond to management direction and solicits feedback to improve performance.</li></ul><p></p><div><br>
</div>
<div><p><i>We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, natural or protective hairstyle, religion, sex, age, national origin, physical or mental disability, sexual orientation, gender identity, genetic information, military service, pregnancy or pregnancy-related condition, or because of marital, parental, or veteran status. We are a VEVRAA Federal Contractor.</i></p></div></div>

PATIENT COORDINATOR, School of Dental Medicine, Clinical Affairs

Optum

<div><p><b>Atrius Health, part of the Optum family of businesses, is seeking a Full Time Psychologist to join our Integrated Behavioral Health Division in Boston, MA. Optum is a clinician-led care organization that is changing the way clinicians work and live.</b></p><p></p><p><b><br>
As a member of the Optum Care Delivery team, you'll be an integral part of our vision to make healthcare better for everyone.</b></p><p></p><p><br>
At Optum, you'll have the clinical resources, data and support of a global organization behind you so you can help your patients live healthier lives. We believe you deserve an exceptional career, and will empower you to live your best life at work and at home. Experience the fulfillment of advancing the health of your community with the excitement of contributing new practice ideas and initiatives that could help improve care for millions of patients across the country. Because together, we have the power to make health care better for everyone. Join us and discover how rewarding medicine can be while<b> Caring. Connecting. Growing together.</b></p><p></p><p><b><br>
Position Highlights &amp; Primary Responsibilities:</b></p><ul><li><p>
Provides mental, behavioral, and/or psychological treatment services or therapy directly to adult patients utilizing a variety of treatment methodologies.</p></li><li><p>
Hybrid Model, 1-2 days on-site and the remaining remote, from your home.</p></li><li><p>
(Electronic equipment included.)</p></li><li><p>
Provide treatment for primary care patients for behavioral health disorders, symptoms and conditions including substance use disorders.</p></li><li><p>
Opportunity for specialty work available: OB/Gyn, women's issues, neurology, concussion team, ADHD, Diagnostic Team; Ortho, chronic pain and substance use</p></li><li><p>
Enhance patient engagement by using evidenced based tools such as cognitive behavioral therapy and motivational interviewing.</p></li><li><p>
Help implement treatment plans with site specific Integrated Clinician and regional Prescribers (Nurse Practitioners and Psychiatrists).</p></li><li><p>
Knowledge of health psychology is preferred.</p></li><li><p>
Experience with substance abuse and addiction is preferred.</p></li></ul><p></p><p><b><br>
What makes an Optum organization different?</b></p><ul><li><p>
Be part of a best-in-class employee experience that enables you to practice at the top of your license</p></li><li><p>
We believe that better care for clinicians equates to better care for patients</p></li><li><p>
We are influencing change collectively on a national scale while still maintaining the culture and community of our local care organizations</p></li><li><p>
Practice medicine autonomously, with the support, not restrictions, of a sustainable and thriving national health care organization</p></li></ul><p></p><p><b><br>
Compensation &amp; Benefits Highlights:</b></p><ul><li><p>
Competitive compensation</p></li><li><p>
Dedicated CME Time &amp; Allowance</p></li><li><p>
Excellent PTO package</p></li><li><p>
Robust retirement package including employer funded contributions</p></li></ul><p></p><p><br>
Atrius Health is a physician-led healthcare leader. We are nationally recognized for transforming healthcare through clinical innovations, quality improvement and a commitment to value-based care. Atrius Health delivers an effective system of connected care at practice locations in eastern and central Massachusetts. We recognize the importance of a team-based delivery model, where primary &amp; specialty care providers collaborate with hospital partners, community specialists and skilled nursing facilities - all working together to deliver high-quality care to every patient we serve. Together, we're making health care work better for everyone.</p><p></p><p><br>
You'll be rewarded and recognized for your performance in an environment that will challenge you and give you clear direction on what it takes to succeed in your role as well as provide development for other roles you may be interested in.</p><p><b>
Required Qualifications:</b></p><ul><li><p>
Clinical Psychologist</p></li><li><p>
Unlimited Licensure in the state of Massachusetts</p></li></ul><p></p><p><b><br>
Preferred Qualifications:</b></p><ul><li><p>
Experience working within an integrated model</p></li><li><p>
Minimum 3 years practice experience</p></li></ul><p></p><p><br>
The salary range for this role is $97,300 to $146,100 annually based on full-time employment. Pay is based on several factors including but not limited to local labor markets, education, work experience, certifications, etc. UnitedHealth Group complies with all minimum wage laws as applicable. In addition to your salary, UnitedHealth Group offers benefits such as, a comprehensive benefits package, incentive and recognition programs, equity stock purchase and 401k contribution (all benefits are subject to eligibility requirements). No matter where or when you begin a career with UnitedHealth Group, you'll find a far-reaching choice of benefits and incentives.</p><p></p><p><i><br>
OptumCare is an Equal Employment Opportunity employer under applicable law and qualified applicants will receive consideration for employment without regard to race, national origin, religion, age, color, sex, sexual orientation, gender identity, disability, or protected veteran status, or any other characteristic protected by local, state, or federal laws, rules, or regulations.</i></p><p></p><p><i><br>
OptumCare is a drug-free workplace. Candidates are required to pass a drug test before beginning employment.</i></p></div>

Clinical Psychologist (Ph.D or Psy.D) | Atrius Health

Boston Medical Center

<div><div><div><h3 class="jobSectionHeader"><b>Clinical Research Coordinator II, Hematology/Oncology</b></h3>
 <div></div><div><div><ul><li>48162
</li> </ul></div><div></div><div><ul><li>650 Albany Street, Boston, Massachusetts
</li> </ul></div><div></div><div><ul><li>Full Time</li></ul></div></div><div></div><div><div><b><br>
</b></div>
</div><div><p><b>Position:</b> Clinical Research Coordinator II, Hematology/Oncology</p><p><b>
Location</b>: Boston, MA</p><p><b>
Schedule</b>: 40 hours per week, On-site</p><p></p><p><b>
ABOUT BMC:</b></p><p></p><p>
At Boston Medical Center (BMC), our diverse staff works together for one goal &mdash; to provide exceptional and equitable care to improve the health of the people of Boston. Our bold vision to transform health care is powered by our respect for our patients and our commitment to ensure everyone who comes through our doors has a positive experience.</p><p></p><p>
You&rsquo;ll find a supportive work environment at BMC, with rich opportunities throughout your career for training, development, and growth.</p><p></p><p><b>
POSITION SUMMARY</b><b>:</b></p><p></p><p>
The Clinical Research Coordinator II will play a key role in supporting research activities within the Translational Research Laboratory and Biospecimen Repository in the Section of Hematology &amp; Medical Oncology. Primary responsibilities include obtaining informed consent for research studies and biobank enrollment, abstracting data from medical records, maintaining patient databases, and processing and managing biospecimen samples. In addition, the CRC will contribute to the generation, organization, and preliminary analysis of research data from ongoing translational studies and support the maintenance and operation of laboratory equipment to ensure high-quality and reproducible research outputs.</p><p></p><p>
Working closely with clinicians, laboratory staff, and collaborating principal investigators, the CRC will ensure all activities are conducted in accordance with institutional policies, IRB regulatory requirements, and ethical research standards. The role also involves assisting with literature reviews, preparing study data and reports, and contributing to manuscript development. <b><i>This position offers hands-on experience in translational cancer research, including biospecimen-based studies and opportunities for co-authorship on abstracts and manuscripts based on contribution.</i></b></p><p></p><p><b>
JOB RESPONSIBILITIES:</b></p><ul>
<li>
Recruit, screen, and obtain informed consent for research studies and biobank participation.</li>
<li>Process, label, store, and ship biospecimens per protocol.</li>
<li>Maintain accurate databases, research records, and regulatory documentation. Perform basic data analysis and prepare figures/tables.</li>
<li>Coordinate study activities with clinical and research teams.</li>
<li>Assist with literature reviews, data summaries, and report/manuscript preparation.</li>
<li>Operate, maintain, and troubleshoot laboratory equipment; coordinate servicing and monitor inventory.</li>
<li>Ensure compliance with all regulatory, privacy, and confidentiality requirements.</li>
</ul><p></p><p><b>
JOB REQUIREMENTS</b></p><p></p><p><b>
EDUCATION / EXPERIENCE:</b></p><p>
CRC II: Experienced Level Position</p><ul>
<li><p>
Master&rsquo;s Degree OR</p></li>
<li><p>
Bachelor&rsquo;s Degree by time of hire plus 2-5 years of experience</p></li>
<li><p>
Special Intermittent Project Responsibilities (2-5 per year)</p></li>
<li><p>
Experience in clinical research, patient recruitment, and biospecimen handling preferred.</p></li>
</ul><p></p><p><b>
KNOWLEDGE AND SKILLS:</b></p><ul>
<li>
Proficiency in Microsoft Office; EMR experience preferred.</li>
<li>Familiarity with data management tools (e.g., REDCap) preferred.</li>
<li>Strong organizational, communication, and multitasking skills.</li>
<li>Ability to work independently and with diverse populations.</li>
<li>Experience with laboratory equipment and SOPs a plus.</li>
</ul><p></p><p><b>
JOB BENEFITS:</b></p><ul>
<li>
Competitive pay</li>
<li>Tuition reimbursement and tuition remission programs</li>
<li>Highly subsidized medical, dental, and vision insurance options</li>
<li>Career Advancement/Professional Development: Access a wealth of ongoing training and development opportunities that will not only enhance your skills but also expand your knowledge base especially for individuals pursuing careers in medicine or biomedical research.</li>
<li>Pioneering Research: Engage in groundbreaking research projects that are driving the forefront of biomedical science.</li>
</ul><p></p><p><b>
ABOUT THE DEPARTMENT:</b></p><p></p><p>
As the primary teaching hospital for Boston University Chobanian &amp; Avedisian School of Medicine and BU schools of public health and dentistry, intellectual rigor shapes our inquiries. Our research is led by a belief that skin color, zip code, and financial circumstances shouldn&rsquo;t dictate health.</p><p></p><p>
Boston Medical Center is an Equal Opportunity/Affirmative Action Employer. If you need accommodation for any part of the application process because of a medical condition or disability, please send an e-mail to Talentacquisition@bmc.org or call 617-638-8582 to let us know the nature of your request.</p><p></p><p><b>
Compensation Range:</b></p>
$42,500.00- $59,500.00<p>
This range offers an estimate based on the minimum job qualifications. However, our approach to determining base pay is comprehensive, and a broad range of factors is considered when making an offer. This includes education, experience, skills, and certifications/licensures as they directly relate to position requirements; as well as business/organizational needs, internal equity, and market-competitiveness. In addition, BMCHS offers generous total compensation that includes, but is not limited to, benefits (medical, dental, vision, pharmacy), discretionary annual bonuses and merit increases, Flexible Spending Accounts, 403(b) savings matches, paid time off, career advancement opportunities, and resources to support employee and family well-being.</p><p><b>
NOTE</b>: This range is based on Boston-area data, and is subject to modification based on geographic location.</p><p></p><p>
Equal Opportunity Employer/Disabled/Veterans</p><p>
According to the FTC, there has been a rise in employment offer scams. Our current job openings are listed on our website and applications are received only through our website. We do not ask or require downloads of any applications, or &ldquo;apps&rdquo; job offers are not extended over text messages or social media platforms. We do not ask individuals to purchase equipment for or prior to employment.</p></div></div></div></div>

Clinical Research Coordinator II, Hematology/Oncology

The General Hospital Corporation

<div>Site: The General Hospital Corporation<p></p><p><br>
Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We believe that high-performing teams drive groundbreaking medical discoveries and invite all applicants to join us and experience what it means to be part of Mass General Brigham.</p><br>
<p></p>
The Advanced Practice Manager is accountable for ensuring the delivery of consistently high-quality patient care and supporting the development of the AMC Program for Substance Use and Addiction Services (PSAS) advanced practice staff. Drawing on a deep understanding of clinical addiction care and PSAS practices and policies, the advanced practice manager will continually assess clinical issues including scope of practice guidelines and practice protocols.<br>
<br>
This role works collaboratively with PSAS&rsquo;s administrative, nursing, and physician leaders, as well as, with each advanced practitioner. S/he will lead and participate in team building, scheduling, ensuring clinical coverage, quality improvement, and staff development. S/he will establish and maintain a professional practice model that supports high quality, efficient care for patients and families in an environment that fosters professional mentorship, collaboration, and support.<br>
<br>
This role reports to the APP Director for Hospital Medicine and will collaborate with the clinical and administrative leadership of PSAS, as well as receive guidance and support from the Chief APP Officer, as well as collaborate with the Associate Chief Nurse for Medicine.<p></p><p><b><br>
Job Summary</b></p>
Summary
<br>
Provides direct management to typically a small to medium-sized team of advanced practice providers or other allied health professionals while continuing to spend the majority of time providing direct patient care as a Nurse Practitioner.<br>
Does this position require Patient Care? Yes<br>
Essential Functions Performs all essential functions of a Nurse Practitioner, providing direct patient care.<br>
<ul><li>Directly oversees and is accountable for the performance of a team of APPs and/or other direct reports.</li><li>Hires, performance manages, and completes performance appraisals for a team of APPs and/or other direct reports.
</li><li>Orients, trains, and schedules staff.
</li><li>Assists with quality assurance programs as needed to help implement quality improvement efforts.
</li><li>Ensures continuing education and teaching for APPs.</li><li>Acts as liaison between the hospital, physician and nursing staff, and other APPs.</li><li>Ensures APPs are following proper billing compliance rules and methodology.</li></ul><p></p><div><div><div><div><div><div><div><p><b><br>
Qualifications</b></p></div></div></div></div></div></div></div><div>
Education<br>
Master's Degree Nursing or Physician Assistant Studies required<br>
<br>
Can this role accept experience in lieu of a degree?<br>
No<br>
<br>
Licenses and Credentials<br>
<ul><li>Currently licensed as a Nurse practitioner or Physician Assistant</li></ul></div><ul><li>Current Federal &amp; Massachusetts licensures to dispense controlled substances</li><li>For nurse practitioners, certification as an Addiction Registered Nurse Advanced Practice, or agreement to get certified within 12 months of hiring is required</li></ul><p><br>
Experience</p><ul><li>5 years&rsquo; experience providing advanced practice level medicine care.</li><li>Effective at leading change, building and leading teams.</li><li>Expertise in executing new programs and clinical operations.</li><li>Ability to mentor, manage and lead within all levels of the organization.</li><li>Effective communicator with the ability to transfer knowledge, orally and in writing.</li><li>Computer skills to support administrative and clinical tasks, to include EHR &amp; Microsoft Office applications.</li></ul><div><br>
Knowledge, Skills and Abilities<br>
<ul><li>Strong clinical knowledge as a Nurse Practitioner.</li><li>Strong managerial presence and ability to provide &amp; direct feedback and guidance to staff.</li><li>Strong interpersonal communication skills.</li><li>Ability to function effectively in a fast-paced environment.</li><li>Results-oriented and exhibits a strong attention to detail.</li></ul></div><p>
Principle Duties and Responsibilities</p><p>
Patient Care Responsibilities:</p><ul><li>Maintains direct patient care weekly in PSAS clinical services.</li><li>Performs duties and responsibilities of an advanced practice nurse or certified physician assistant with expertise in Addiction care.</li></ul><p></p><p>
Supervises and coordinates the work of inpatient and outpatient advance practitioners in PSAS to provide the highest quality of care to patients and meet the goals/needs of the program:</p><ul><li>Interviews and hires new staff in collaboration with PSAS administrative and physician leaders.</li><li>Ensures all advanced practitioners are appropriately credentialed and licensed.</li><li>Establishes and/or maintains orientation and training materials appropriate for each role group and in accordance with regulatory requirements. Provides competency-based orientation for all new staff.</li><li>Provides coaching and evaluates performance, completes annual evaluations, and ensures competency and ongoing compliance with job requirements and standards. Develops and implements remediation and corrective action plans when needed.</li><li>Develops APP staffing patterns, required personnel complements to meet the needs of the patient population, and APP scheduling.</li><li>Is accountable for ensuring coverage plans for scheduled and unscheduled leaves of absence and vacation.</li><li>Directs the development and implementation of professional development programs for advanced practice staff, using established and newly created mechanisms.</li><li>Leads regular advanced practice staff meetings to ensure priorities &amp; goals, regulatory requirements, new policies &amp; procedures, and training are communicated and shared.</li><li>Attends team rounds regularly.</li></ul><p></p><p>
Collaborates and communicates with physician, nursing, and administrative leadership:</p><ul><li>Participates in strategic planning, priority-setting, decision-making, fiscal planning, and process improvement efforts related to PSAS.</li><li>Participates and leads development/enhancement of existing and future clinical programs and implementation of process improvements.</li><li>Plans, directs, and participates in regularly scheduled meetings to share information and problem solve with PSAS personnel.</li><li>Collaborates with nursing and hospital educational resources to facilitate learning experiences for staff.</li></ul><p></p><p>
Contributes to management/leadership discussions/efforts:</p><ul><li>Participates in the planning of PSAS, including but not limited to operational, clinical, and fiscal design with a particular focus on clinical operations and workflow for advanced practice staff.</li><li>Participates in Operational problem-solving regarding staffing models, support structures, coverage models, and needs assessment.</li><li>Meets regularly with physician, nursing, and administrative leaders regarding specific patient populations/needs, and innovations.</li><li>Participates in manager meetings and institutional committees as appropriate.</li><li>Acts as a liaison for communication of APP specific topics to unit and departmental physician and administrative leadership.</li><li>Participates in departmental operations meetings for planning, innovation, and coverage model considerations moving forward as needed.</li><li>Manages all APP staff to enhance and progress the goals of the program, the division and the department.</li><li>Attend relevant multidisciplinary rounds at MGH as needed to advance addiction care.</li><li>Serve as a local subject matter expert, including delivering educational content and training as needed.</li><li>Assist with scheduling and ensure supervision for APP trainees.</li><li>Attend system HRO rounds when SUD goals are on the scorecard at MGH, and other sites as needed based on direction from the Director or Associate Director of PSAS.</li><li>Assist with implementation of quality improvement interventions at MGH to meet MGB goals, including managing patient surveillance workflows as needed.</li><li>Assist with other PSAS clinical leadership needs as requested.</li></ul><p></p><p>
Provides effective patient-focused advanced practice care.</p><ul><li>Sets standards for clinical care provided by Nurse Practitioners and Physicians Assistants; monitors, measures and advances patient care; serves as an exemplary provider handling the most complex cases and advising staff as needed.</li><li>Assists the staff in the provision of care using, but not limited to, the philosophy of PSAS, MGH, the Division of General and Internal Medicine, and Joint Commission standards of care.</li><li>Maintains competence in Addiction advanced practice care, serving as a clinical role model to staff.</li><li>Provides direct patient care to assigned patient population</li><li>Promotes an environment that is sensitive to the culturally diverse needs of patients and staff.</li></ul><p></p><p>
Hospital Resource</p><ul><li>Participates as an active member of the MGH APP Leadership Council</li><li>Increases PSAS footprint through system wide committee and leadership opportunities</li><li>Participates in problem solving and innovative opportunities for growth of the APP community, recognition of staff.</li></ul><p></p><div><div><div><div><div><div><div><p><b><br>
Additional Job Details (if applicable)</b></p></div></div></div></div></div></div></div><p>
Working conditions:</p><ul><li>Local travel to Mass General Brigham sites may be required.</li><li>This role is hybrid but requires the ability to be in person for administrative time as needed.</li><li>Work is performed in an acute care hospital setting. The work may require the lifting of heavy objects and patients, as well as exposure to potentially infective material. Work requires contact with needles and other sharp instruments, monitoring devices, and other state-of-the-art</li></ul><p>
equipment. Prolonged standing can be expected. Walking to and from the patient care units can be expected.</p><p></p><div><div><div><div><div><div><div><p><b><br>
Remote Type</b></p></div></div></div></div></div></div></div>
Hybrid<p></p><div><div><div><div><div><div><div><p><b><br>
Work Location</b></p></div></div></div></div></div></div></div>
55 Fruit Street<p></p><div><div><div><div><div><div><div><p><b><br>
Scheduled Weekly Hours</b></p></div></div></div></div></div></div></div>
40<p></p><div><div><div><div><div><div><div><p><b><br>
Employee Type</b></p></div></div></div></div></div></div></div>
Regular<p></p><div><div><div><div><div><div><div><p><b><br>
Work Shift</b></p></div></div></div></div></div></div></div>
Day (United States of America)<p></p><p><b><br>
Pay Range</b></p>
$130,249.60 - $190,278.40/Annual<p></p><p><b><br>
Grade</b></p>
8<br>
<p></p>
At Mass General Brigham, we believe in recognizing and rewarding the unique value each team member brings to our organization. Our approach to determining base pay is comprehensive, and any offer extended will take into account your skills, relevant experience if applicable, education, certifications and other essential factors. The base pay information provided offers an estimate based on the minimum job qualifications; however, it does not encompass all elements contributing to your total compensation package. In addition to competitive base pay, we offer comprehensive benefits, career advancement opportunities, differentials, premiums and bonuses as applicable and recognition programs designed to celebrate your contributions and support your professional growth. We invite you to apply, and our Talent Acquisition team will provide an overview of your potential compensation and benefits package.<p></p><div><div><div><div><div><div><div><p><b><br>
EEO Statement:</b></p></div></div></div></div></div></div></div>
1200 The General Hospital Corporation is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law. We will ensure that all individuals with a disability are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. To ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veteran&rsquo;s Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact Human Resources at (857)-282-7642.<p></p><h2 class="jobSectionHeader"><b><br>
Mass General Brigham Competency Framework</b></h2><div><div><p>
At Mass General Brigham, our competency framework defines what effective leadership &ldquo;looks like&rdquo; by specifying which behaviors are most critical for successful performance at each job level. The framework is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success. These competencies are used to evaluate performance, make hiring decisions, identify development needs, mobilize employees across our system, and establish a strong talent pipeline.</p></div></div></div>

APP Manager - PSAS - MGH

Dana-Farber Cancer Institute

<div><div><div><div>Job Ref:</div><div>
JR-3478</div></div><br>
<div><div>Location:</div><div>
450 Brookline Ave, BOSTON, MA 02215</div><br>
</div>
<div><div>Category:</div><div>
Clinical Research</div></div><br>
<div><div>Employment Type:</div><div>
Full time</div></div><br>
<div><div>Work Location:</div><div>
Onsite: occasional remote</div></div><br>
<div></div><div><div>Salary/Pay Rate:</div><div>
$48,100.00 - $54,400.00 per year</div>
</div></div><p><b>Overview</b></p>
<p></p><div><div>The Gastrointestinal (GI) Oncology Clinical Research Program at Dana-Farber Cancer Institute is seeking a Clinical Research Coordinator (CRC) to join our program. The GI Oncology Clinical Research Program supports PI initiated, industry sponsored, and cooperative group phase I - IV clinical trials across multiple GI cancers, including esophageal, stomach, liver, pancreas, colon, and neuroendocrine.<br>
<br>
The Clinical Research Coordinator work within the clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator. The CRC will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials. Ensures timely collection of protocol related samples including shipment to outside entities as required. Maintains regulatory binders and ensures study compliance with all state, federal, and IRB requirements. May be responsible for IRB protocol submissions (amendments, continuing reviews, and minimal risk protocols). This individual may also screen patients for protocol eligibility, obtain informed consent, and register study participants with the Quality Assurance Office for Clinical Trials (QACT). Some travel may be required.<p>
Located in Boston and the surrounding communities, Dana-Farber Cancer Institute is a leader in life changing breakthroughs in cancer research and patient care. We are united in our mission of conquering cancer, HIV/AIDS, and related diseases. We strive to create an inclusive, diverse, and equitable environment where we provide compassionate and comprehensive care to patients of all backgrounds, and design programs to promote public health particularly among high-risk and underserved populations. We conduct groundbreaking research that advances treatment, we educate tomorrow's physician/researchers, and we work with amazing partners, including other Harvard Medical School-affiliated hospitals.</p><br>
<ul><li>
Oversight of the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities.</li><li>
Responsible for data reporting and management, collection of source documents, use and development of case report forms, adverse events reporting, filing, and archiving of study records, and resolution of data queries.</li><li>
May prepare and or complete regulatory related reports and IRB submissions. Maintain and organize study participant/subject trial binder and regulatory binders, enter all required study data on an ongoing basis and as applicable.</li><li>
Ensure all study related samples are collected, properly prepared, and shipped according to the protocol requirements and IATA/DOT regulations.</li><li>
Collaborate with other departments such as Protocol Scheduling, Materials Management, the Clinical Research Laboratory, Pharmacy, Research Nursing, and other departments, as needed per the requirements of the clinical trial.</li><li>
Responsible for organizing and preparing for both internal and external auditing and study monitoring visits.</li><li>
Coordination and management of clinical trials throughout the trial life cycle, including communication with sponsors and regulatory authorities.</li><li>
Close-out of clinical trials, including contributing to research articles, audit preparation, and communication with regulatory agencies and other disciplines involved.</li><li>
Interact with study participants as directed/required by the protocol and/or study team.</li><li>
May be responsible for tissue sample collection per trial requirements.</li><li>
Responsible for data entry of Subject Visit Tracking information into Clinical Trial Management System contemporaneously with medical visits, assessments, and other subject-specific information.</li><li>
Responsible for data entry of time and effort spent on study-specific activities and other administrative tasks into Clinical Trial Management System contemporaneously with work completed.</li><li>
Responsible for data entry of study-specific activity, including but not limited to monitor visits, external site enrollment, amendments, receipt of Safety Reports, etc. into Clinical Trial Management System contemporaneously with activity completed.</li></ul><p><b>
KNOWLEDGE, SKILLS, AND ABILITIES REQUIRED:</b></p><ul><li>
Excellent organization and communications skills required.</li><li>
Strong interpersonal skills &ndash; ability to effectively interact with all levels of staff and externals contacts.</li><li>
Must be detail oriented and have the ability to follow-through.</li><li>
Ability to effectively manage time and prioritize workload.
</li><li>Must practice discretion and adhere to hospital confidentiality guidelines at all times.</li><li>
Must have computer skills including the use of Microsoft Office.</li></ul><p><b>
MINIMUM JOB QUALIFICATIONS:
</b></p><ul><li>Bachelor&rsquo;s Degree or 1 year of Dana-Farber Associate Clinical Research Coordinator experience required. 0-1 years of experience working in a medical or scientific research setting or comparable technology orientated business environment preferred.
</li></ul><p><b>SUPERVISORY RESPONSIBILITIES: None</b></p><p><b>
PATIENT CONTACT:
</b></p><p><b>All positions: </b>May have contact with Adult and Pediatric patients of all ages and populations. May distribute protocol schedules, quality of life surveys or other study-related questionnaires, subject diaries, and/or conduct follow-up communication with patients</p><p>
At Dana-Farber Cancer Institute, we work every day to create an innovative, caring, and inclusive environment where every patient, family, and staff member feels they belong. As relentless as we are in our mission to reduce the burden of cancer for all, we are committed to having faculty and staff who offer multifaceted experiences. Cancer knows no boundaries and when it comes to hiring the most dedicated and compassionate professionals, neither do we. If working in this kind of organization inspires you, we encourage you to .</p><p>
Dana-Farber Cancer Institute is an equal opportunity employer and affirms the right of every qualified applicant to receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, national origin, sexual orientation, genetic information, disability, age, ancestry, military service, protected veteran status, or other characteristics protected by law.
</p><h3 class="jobSectionHeader"><b>EEO Poster</b></h3>
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Pay Transparency Statement</p><p>
The hiring range is based on market pay structures, with individual salaries determined by factors such as business needs, market conditions, internal equity, and based on the candidate&rsquo;s relevant experience, skills and qualifications.</p><p>
For union positions, the pay range is determined by the Collective Bargaining Agreement (CBA).</p>
$48,100.00 - $54,400.00</div></div></div><p></p>

Clinical Research Coordinator - GI Oncology

Tufts Medical Center

<div><div><p><b>General Summary:</b></p><p>
The CardioVascular Center (CVC) integrates the clinical services of Cardiology,<br>
Cardiac Surgery, Vascular Surgery, Interventional Radiology and Anesthesiology<br>
under a single, collaborative, inter-disciplinary organizational umbrella and it has<br>
an academic mission centered in its CardioVascular Center Research Institute<br>
(CVCRI). It offers a full range of primary-through-quaternary cardiovascular<br>
services, with over 3,300 cardiovascular hospital discharges and over 16,000<br>
ambulatory visits annually. The CVC has the infrastructure needed to support its<br>
highly robust and productive clinical research efforts in vascular diseases, heart<br>
failure and transplant, mechanical circulatory support, interventional cardiology,<br>
cardiac arrhythmia, hypertrophic cardiomyopathy, cardiac imaging, cardiovascular surgery, and preventive cardiology.</p><p><br>
This position will support the research of Dr. Margaret Infeld. As a Clinical<br>
Research Coordinator, this role will manage clinical research projects funded by<br>
industry as well as investigator led trials. The candidate will be responsible for<br>
managing and assisting the Principal Investigator and research team in the<br>
coordination of all activities of studies as required for successful implementation of the study protocol(s) and interpretation of study findings.</p><p></p><p><b>
Job Overview</b></p><p>
This position will assist the Principal Investigator (PI) in planning and implementing clinical research studies as assigned.</p><p></p><p><b>
Job Description</b></p><p><b>
Minimum Qualifications:</b></p><p>
1. Bachelor&rsquo;s degree OR High School Diploma or equivalent <b>AND</b> Four (4) years of related experience.</p><p>
2. Basic Life Support (BLS) certification may be required based on specific role requirements.</p><p></p><p><b>
Preferred Qualifications:</b></p><p>
1. Two (2) years in research related activities.</p><p>
2. IATA Hazardous Good Shipping certification.</p><p>
3. CITI Human Research Protection certification.</p><p></p><p><b>
Duties and Responsibilities:</b> The duties and responsibilities listed below are intended to describe the general nature of work and are not intended to be an all-inclusive list. Other duties and responsibilities may be assigned.</p><p></p><p>
1. Assists in the recruitment of study participants.
</p><p>2. Completes follow up with study participants in prescribed settings as required.</p><p>
3. Completes record abstraction of source documents, conducting required study measurements and completing study Case Report Forms in accordance with best practice methods.
</p><p>4. Complies with all institutional policies and government regulations pertaining to human subjects protections. Maintains regulatory binders, case report forms, source documents, and other study documents. Monitors the occurrence of clinical adverse events, reporting any to the (PI), the study sponsor and Institutional Review Board.</p><p>
5. Assists with Institutional Review Board (IRB) requirements for each study including meeting institutional educational requirements, submitting documents for review such as amendments, adverse event reporting and annual reviews.</p><p>
6. Performs basic laboratory activities as needed.</p><p>
7. Maintains patient confidentiality per HIPAA regulations and keeps study information in a safe and secure location. Adheres to FDA Good Clinical Practice Guidelines.</p><p>
8. Identifies and resolves problems with protocol compliance by notifying investigator and as necessary with the protocol sponsor.</p><p>
9. Arranges necessary tests and procedures in accordance with protocol requirements and reports results to the investigator.</p><p>
10. Participates in site visits with the study sponsor to review completeness and accuracy of study documentation.
</p><p>11. Maintains inventory of all study supplies.</p><p>
12. Assesses potential patients and eligibility for inclusion in a particular protocol based on protocol requirements.</p><p>
13. Reviews all eligibility and ineligibility criteria in the patient&rsquo;s record.</p><p>
14. Verifies information with the physician.</p><p>
15. Interviews patients to obtain information for eligibility assessment, explain the study, and obtains signature for the informed consent form.</p><p>
16. Conducts a QC check of completed CRFs prior to submission for data entry.</p><p>
17. Coordinates resolution of all data queries.</p><p>
18. Completes data entry as warranted.</p><p>
19. Performs necessary tests as needed and as appropriate to level of training such as EKGs, Walk tests, etc.</p><p></p><p><b>
Physical Requirements:</b></p><p>
1. Typical clinical and administrative office setting.</p><p></p><p><b>
Skills &amp; Abilities:</b></p><p>
1. High degree of organizational talents, data collection, and analysis skills.</p><p>
2. Requires meticulous attention to detail.</p><p>
3. Excellent computer skills including word processing.</p><p>
4. Ability to prioritize quickly and appropriately.</p><p>
5. Excellent communication and interpersonal skills.</p><p>
6. Systematic record-keeping.</p></div><p></p><p><br>
At Tufts Medicine, we want every individual to feel valued for the skills and experience they bring. Our compensation philosophy is designed to offer fair, competitive pay that attracts, retains, and motivates highly talented individuals, while rewarding the important work you do every day.</p><p></p><p>
The base pay ranges reflect the minimum qualifications for the role. Individual offers are determined using a comprehensive approach that considers relevant experience, certifications, education, skills, and internal equity to ensure compensation is fair, consistent, and aligned with our business goals.</p><p></p><p>
Beyond base pay, Tufts Medicine provides a comprehensive Total Rewards package that supports your health, financial security, and career growth&mdash;one of the many ways we invest in you so you can thrive both at work and outside of it.</p><p></p><p><b><br>
Pay Range</b><b>:</b></p><br>
<p></p>
$44,778.55 - $55,978.47</div>

Clinical Research Coordinator I - CardioVascular, Electrophysiology

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