132 jobs found in Sanford, ME

The Pharmacist, Research Specialist supports patient care by understanding the clinical trial research protocol, providing clinical trial education to the pharmacy staff, coordinating study drug inventory/supplies, and assisting sites with any operational and regulatory concerns related to the clinical trial. This position will rotate primarily across Londonderry, NH; Methuen, MA; Brighton, MA; and Weymouth, MA. Additional coverage may be required, as needed, in Foxborough, MA; Milford, MA; and Attleboro, MA. 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...

The Clinical Research Coordinator (CRC) will work within the Dana-Farber Londonderry, NH Satellite 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(s) and the DFCI disease programs. The Satellite CRC will be responsible for the primary data collection, management of patient clinical information, and regulatory documents as it pertains to participation in clinical trials across all studies open at the Satellite site(s). Ensures timely collection of protocol related samples including shipment to outside entities as required. Maintains site regulatory binders and ensures study compliance with all state, federal, and IRB requirements. May be responsible for site IRB submissions (violations, deviations, severe adverse event reports). This individual may also screen patients for protocol eligibility, obtain informed consent (minimal risk studies), and register...

When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. Responsible for screening patients for participation in clinical drug trials, enrolling patients onto these studies, monitoring protocol implementation, completing required forms and reporting results. Job Description: Primary Responsibilities: 1. Independently or in conjunction with other clinical research staff and/or research nurse, recruits and enrolls research subjects onto clinical research projects according to study protocols. May assess research subjects' eligibility for inclusion in a particular protocol based on contracts with physicians and nurses and knowledge of the protocol. (essential) 2. Checks all eligibility and ineligibility criteria with the research subjects' medical record. Verifies information with clinical research nurse and/or principal investigator. (essential) 3. Discusses informed consent with research subjects....

When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. This position will focus on research related to the Electrophysiology and Cardiac Catheterization labs. Job Description: Primary Responsibilities: 1. Independently or in conjunction with other clinical research staff and/or research nurse, recruits and enrolls research subjects onto clinical research projects according to study protocols. May assess research subjects' eligibility for inclusion in a particular protocol based on contracts with physicians and nurses and knowledge of the protocol. (essential) 2. Checks all eligibility and ineligibility criteria with the research subjects' medical record. Verifies information with clinical research nurse and/or principal investigator. (essential) 3. Discusses informed consent with research subjects. Interacts with research subjects prior to entering the study and throughout the entire treatment....

When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. Functioning independently with minimal supervision and direction, will be responsible for coordinating multiple research studies by implementing study protocols in accordance with regulatory, departmental and institutional requirements. Provides mentoring, direction, supervision and guidance to Clinical Research Coordinators. May serve as a project manager or team lead with supervisory responsibilities. Performs diverse duties requiring analysis, sound judgment and a high level of knowledge of specific protocols. Maintains interdisciplinary relationship with participating physicians and clinical departments. Interacts with study participants diagnosed with various medical conditions and diagnoses. Job Description: Minimum Qualifications: Education: Bachelor’s degree required; Master’s degree preferred. 5+ years of relative experience. In...

When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. Under general supervision and direction will be responsible for the coordination and administration of multiple research studies. Works closely with principal investigators and research staff facilitating all aspects of assigned clinical trials. Implements study protocols in accordance to regulatory and institutional requirements. Sets up administrative systems to manage the progress of each study while screening, recruiting and following study participants and collecting and reporting study data. Interacts with study participants diagnosed with various medical conditions and diagnoses. Job Description: Minimum Qualifications:     Education :   Bachelor’s degree required .     Licensure, Certification & Registration :   None required.   Experience : 0-2 years of experience in...

When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. Job Description: Responsible for screening patients for participation in clinical trials, enrolling patients onto these studies, monitoring protocol implementation, completing required forms and reporting results. This position has a flexible schedule which may require evenings and weekends as needed. Primary Responsibilities: 1. Independently or in conjunction with other clinical research staff and/or research nurse, recruits and enrolls research subjects onto clinical research projects according to study protocols. May assess research subjects' eligibility for inclusion in a particular protocol based on contracts with physicians and nurses and knowledge of the protocol. (essential) 2. Checks all eligibility and ineligibility criteria with the research subjects' medical record. Verifies information with clinical research nurse and/or principal...

When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. The Hypertrophic Cardiomyopathy (HCM) team at Lahey Hospital and Medical Center is currently seeking an experienced clinical research coordinator to join our research team. HCM is the most common inherited heart condition with a prevalence of 1:500 globally and remains the most common cause of sudden death in young patients and a major cause of heart failure in patients of all ages. The HCM center at Lahey Hospital & Medical Center is one of the most experienced and comprehensive in the world. Recognized as an international Center of Excellence, the Lahey HCM Center is at the leading edge of research on this disease. The clinical research coordinator will be responsible for the coordination and administration of multiple research studies related HCM. Implements and creates study protocols in accordance to regulatory and institutional requirements. Works...

When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. Under minimal supervision and direction will be responsible for the coordination and administration of multiple research studies. Responsible for assigned research studies and general research duties. Implements study protocols in accordance to regulatory and institutional requirements. Works closely with principal investigators, research staff and Research Administration facilitating all aspects of assigned clinical trials. Interacts with study participants diagnosed with cardiovascular disease. Job Description: 1) Possesses ongoing knowledge of FDA, OHRP and GCP regulations: Ensures adherence to regulations. Educates and mentors other study staff as applicable. 2) Responsible for coordinating different phases of research studies with varying degrees of complexity with minimal oversight: Completes and submits trial feasibility forms;...

When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. The Clinical Research Coordinator I will be responsible for the coordination and administration of multiple research studies. Works closely with principal investigators and research staff facilitating all aspects of assigned clinical trials. Implements study protocols in accordance to regulatory and institutional requirements. Sets up administrative systems to manage the progress of each study while screening, recruiting and following study participants and collecting and reporting study data. Interacts with study participants diagnosed with various medical conditions and diagnoses. Job Description: Essential Duties & Responsibilities including but not limited to:   Completes new coordinator orientation and all required trainings.   Responsible for coordinating different phases of research studies with varying degrees of complexity with moderate...

When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. CHIEF MEDICAL PHYSICIST Under the direction of the Radiology Director and the Chief of Radiation Oncology, provides professional medical physics for the Radiation Oncology service. Assumes a lead position in planning and establishing a treatment planning and dosimetry service. Evaluates and interprets medical radiation treatment prescriptions. Collaborates with radiation oncologists in the design and modification of effective radiation treatments for patients; oversees and monitors treatment plans developed by dosimetrists, and establishes an effective quality assurance program for the service. Job Description: Responsibilities: In cooperation with the Radiology Director, Radiation Oncologists, Therapist Manager, and Nurse Manager of Hematology/Oncology establishes the treatment planning service. Evaluates planning and simulation software and...

The Assistant Clinical Research Manager (ACRM) position will work within the Center of Early Detection & Intervention Blood Cancers (CEDI BC) Interventional Clinical Trials clinical research program and assist in the management of the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator. These positions, in collaboration with the program’s Clinical research Managers physicians and research nursing staff, are responsible for assisting with the design, implementation and evaluation of their program’s clinical research activities, related regulatory oversight, and will provide day to day supervision of their program’s clinical research staff as needed. This position’s work location is hybrid with two or three days per week onsite/remote. The selected candidate may only work remote days from a New England state (ME, VT, NH, MA, CT, RI). Located in Boston and the surrounding communities, Dana-Farber...

Investigators in the Division of Cancer Genetics and Prevention at the Dana-Farber Cancer Institute seek a full-time Clinical Research Coordinator to assist in clinical and non-clinical research studies related to cancer prevention, genetic testing, early identification of individuals at high-risk of cancer, and biorepository collections. 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 facilitation of trial assessments per protocol and collection of protocol related samples including shipment to outside entities as required. Will support and maintain participant/subject trial binders and may maintain regulatory binders, to ensure study compliance with all state, federal, and IRB requirements. This individual will also screen patients for protocol eligibility, obtain informed consent for non-treatment trials, and register study participants with the clinical...

Our Population Sciences team is seeking a Research Assistant I (Per Diem) to complete a study. This role supports population sciences research by helping coordinate study activities across internal and external sites, assisting with participant recruitment and enrollment, and supporting surveys, interviews, and other project-related tasks. The Research Assistant will also provide logistical, administrative, and regulatory support, including maintaining study databases and documentation, preparing for meetings, assisting with IRB materials, and conducting literature reviews. The ideal candidate will have strong organizational, communication, and interpersonal skills, along with excellent attention to detail and the ability to work effectively with diverse patient and community populations while maintaining the confidentiality of study materials and data. Please note that only candidates located in Massachusetts, New Hampshire, Connecticut, or Rhode Island will be considered....

The Research Data Specialists will support the Breast Oncology clinical research program in the areas of data collection, computing, and database organization. Duties include the examination, synthesis, and evaluation of medical records; the abstraction and recording of pertinent medical information; and the monitoring of patient status. The Clinical Research Data Specialist will be responsible for the collection, management, and quality assurance review of patient clinical data. This position’s work location is onsite, full-time on campus in Boston, MA in the Longwood Medical Area. 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...

The Pharmacy Department at the Dana-Farber Cancer Institute places emphasis on the values of reliability, professionalism, cooperation, teamwork, communication, positivity and inclusiveness. The Pharmacy Technician III, Research is responsible for providing technical support to research pharmacy operations under the supervision of a licensed pharmacist. The Pharmacy Technician III, Research responsibilities include regulatory and compliance duties such as projects, audits and process improvement initiatives. The Pharmacy Technician III, Research conducts the training and orientation processes of new pharmacy employees and may staff in other pharmacy locations/areas as required 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...

The Pharmacy Department at the Dana-Farber Cancer Institute places emphasis on the values of reliability, professionalism, cooperation, teamwork, communication, positivity and inclusiveness.  The Pharmacy Technician III, Research is responsible for providing technical support to research pharmacy operations under the supervision of a licensed pharmacist.  The Pharmacy Technician III, Research responsibilities include regulatory and compliance duties such as projects, audits and process improvement initiatives.  The Pharmacy Technician III, Research conducts the training and orientation processes of new pharmacy employees and may staff in other pharmacy locations/areas as required. 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...

The Pharmacy Department at the Dana-Farber Cancer Institute places emphasis on the values of reliability, professionalism, cooperation, teamwork, communication, positivity and inclusiveness. The Pharmacy Technician I, Research is responsible for providing technical support to research pharmacy operations under the supervision of a licensed pharmacist. 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,...

The Perini Family Survivors’ Center at Dana-Farber Cancer Institute is seeking a full-time Research Assistant II to join the team. This hybrid role includes both on-site and remote work and supports a research program focused on the psychosocial and physical health outcomes of adult and childhood cancer survivors. Ongoing projects include online interventions targeting anxiety, insomnia, and sexual health, as well as survey-based studies examining mental and physical health outcomes. The Research Assistant II will contribute to multiple active studies and play an important role in day-to-day research operations. Key responsibilities include participant recruitment, eligibility screening, enrollment, telephone interviewing, development of online surveys and study materials, support for live telehealth interventions, mailings, data entry, and database management. Additional duties include conducting literature reviews, abstracting medical records, assisting with presentations and...

The CRC (Clinical Research Coordinators) 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 and the Clinical Research Manager. 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 facilitation of trial assessments per protocol and collection of protocol related samples including shipment to outside entities as required. Will support and maintain participant/subject trial binders and may maintain regulatory binders, to ensure study compliance with all state, federal, and IRB requirements. May be responsible for pertinent IRB protocol submissions. This individual may also screen patients for protocol eligibility, obtain informed consent for non-treatment trials, and register study participants with the clinical trials...