- Ability to understand and follow institutional SOPs.
- Review and assess protocol (including amendments) for clarity, logistical feasibility
- Ensure that all training and study requirements are met prior to trial conduct.
- Discuss study medication, required procedures, eligibility criteria and impact on office flow with Investigator and site staff.
- Assist with planning and creation of appropriate recruitment materials.
- Assist in development of recruitment plan and obtain listing of potential candidates to contact from subject database.
- Actively work with recruitment team in calling and recruiting subjects
- Attend Investigator meetings as required.
- Coordinate and attend pre-study site visits, site initiation visits, and monitor visits with clinical staff and Sponsor/CRO representatives.
- Assist in the creation and review of source documents.
- Prioritize activities with specific regard to protocol timelines
- Maintain adherence to FDA regulations and ICH guidelines in all aspects of conducting clinical trials.
- Maintain effective relationships with study participants and other care Access Research personnel.
- Interact in a positive, professional manner with patients, sponsor representatives, investigators and Care Access Research personnel and management.
- Communicate clearly verbally and in writing
- Prescreen study candidates
- Obtain informed consent per Care Access Research SOP .
- Complete visit procedures in accordance with protocol.
- Train others and complete basic clinical procedures, such as blood draws, vital signs, ECGs, etc.
- Review laboratory results, ECGs, and other test results (e.g., MRIs) for completeness and alert values, ensuring investigator review in a timely fashion.
- Record data legibly and enter in real time on paper or e-source documents
- Accurately record study medication inventory, medication dispensation, and patient compliance.
- Resolve data management queries and correct source data within sponsor provided timelines
- Assist regulatory personnel with completion and filing of regulatory documents.
- This is an on-site position with regional commute requirements. Regularly planned travel within the region will be required as part of the role.
- Excellent working knowledge of medical and research terminology
- Excellent working knowledge of federal regulations, good clinical practices (GCP)
- Ability to communicate and work effectively with a diverse team of professionals.
- Strong organizational, prioritization and leadership skills and capabilities with a strong attention to detail
- Strong computer skills with demonstrated abilities using clinical trials database, IVR systems, electronic data capture, MS word and excel.
- Critical thinker and problem solver
- Friendly, outgoing personality; maintain a positive attitude under pressure.
- High level of self-motivation and energy
- Excellent professional writing and communication skills
- Ability to work independently in a fast-paced environment with minimal supervision
- Bachelor's Degree preferred, or equivalent combination of education, training and experience.
- A minimum of 3 years prior Clinical Research Coordinator experience required
- Prefer 1 year of experience as a Care Access Research Clinical Research Coordinator
- Recent phlebotomy experience requiredBenefits (US Full-Time Employees Only)
- PTO/vacation days, sick days, holidays.
- 100% paid medical, dental, and vision Insurance. 75% for dependents.
- HSA plan
- Short-term disability, long-term disability, and life Insurance.
- Culture of growth and equality
- 401k retirement planDiversity & InclusionWe serve patients and researchers from diverse cultures and communities around the world. We are stronger and better when we build a team representing the people we aim to support. We maintain an inclusive culture where people from a broad range of backgrounds feel valued and respected as they contribute to our mission. We value diversity and believe that unique contributions drive our success. We do not discriminate based on race, sex, religion, color, national origin, gender identity, age, marital status, veteran status, or disability status.
-
Clinical Research Coordinator
2 weeks ago
Articularis Healthcare Summerville, United StatesJob Description · Job DescriptionSalary: · Articularis Healthcare Group (AHG) is currently seeking a full-time Clinical Research Coordinator in our Summerville, SC location. · Our Benefits: · 4-day work week · Benefits package that includes group medical, dental, vision, short ...
-
Clinical Research Coordinator-Dorchester, MA
3 weeks ago
Care Access Dorchester, United StatesWhat We Do · Care Access is delivering the future of medicine today Care Access has a revolutionary model that breaks down traditional barriers to clinical trials that limit participation among physicians and patients to 3%. By removing this bottleneck, Care Access is helping ac ...
-
Coordinator Clinical Research RN
5 days ago
MUSC Charleston, SC, United States Full timeMedical University Hospital Authority (MUHA) · CC000728 CHS - Transplant - Kidney Adult (Main) · Hourly · Health-29 · Work Shift · Under general supervision, the Clinical Transplant Coordinator II develops and uses advanced clinical management, consultation, education and resea ...
-
Coordinator Clinical Research RN
5 days ago
MUSC Charleston, SC, United States Full timeUnder general supervision, the Transplant RN Coordinator develops and uses advanced clinical management, consultation, education and research to promote quality care for the specific transplant patient populations. Provides growth in clinical knowledge through research-based prac ...
-
Coordinator Clinical Research RN
5 days ago
MUSC Charleston, SC, United StatesUnder general supervision, the Transplant RN Coordinator develops and uses advanced clinical management, consultation, education and research to promote quality care for the specific transplant patient populations. Provides growth in clinical knowledge through research-based prac ...
-
Dialysis LPN
3 weeks ago
FRESENIUS MEDICAL CENTER Dorchester, United StatesPOSITION FEATURES: · Location: 2100 Dorchester Avenue, Suite 1S, Boston, MA · Clinic hours: MWF - 5AM-9PM and TTS- 5AM-4PM ( no Sundays) · 2021 and 2022 America's 'Most Loved Workplaces' by Newsweek · Outpatient offers NO: Overnight, Sunday or on-call shifts, major holidays off ...
-
Communications Coordinator
3 weeks ago
Zoo New England Dorchester, United StatesJob Description · Job DescriptionSalary: $24/hour · The Communications Coordinator is responsible for working on a wide variety of communication materials and initiatives to advance the visibility of Zoo New England's Franklin Park Zoo and Stone Zoo through impactful storytelling ...
-
RN - RSFH Oncology, Infusion - Summerville
3 weeks ago
Roper St. Francis Summerville, United StatesThank you for considering a career atRoper St. Francis Healthcare · Schedule: Monday-Friday; 8:00 AM - 5:00 PM · Summary of Primary Function · Delivers patient care utilizing the nursing process through data collection and assessment, identifies and determines the priority of pa ...
-
Corporate Sponsorship Coordinator
2 weeks ago
Zoo New England Dorchester, United StatesJob Description · Job DescriptionSalary: $60,000/annually · Reporting to the Director of Corporate Partnerships, this position is responsible for securing and expanding sponsorships/corporate partnerships and managing partner benefits and fulfillment. The Sponsorship Coordinator ...
-
Senior Foundation Relations Manager
2 weeks ago
Zoo New England Dorchester, United StatesJob Description · Job DescriptionSalary: Responsible for all aspects of raising support from foundations, corporate foundations, and government sources. · Responsible for securing grant support for unrestricted funding and restricted program support. · Establish long-term partne ...
-
School Psychologist
2 weeks ago
Dorchester School Summerville, United StatesPosition Type: · High School-Certified/High School Psychologist · Date Posted: · 5/15/2024 · Location: · East Edisto Middle School · Date Available: · July 25, 2024 · Closing Date: · Until Filled · TITLE: · School-Based Psychologist · SALARY: · As determined by DD2 Certifie ...
-
Behavior Intervention Specialist
2 weeks ago
Dorchester School District 2 Summerville, United StatesPosition Type: · High School-Certified · Date Posted: · 3/18/2024 · Location: · RISE Academy · Date Available: · August 2024 · Closing Date: · Open Until FilledTITLE: · Behavior Intervention Specialist · SALARY: · As determined by DD2 Teacher Salary Schedule · DEPARTMENT: · The R ...
-
Civil Engineering Project Manager
1 day ago
SeamonWhiteside Summerville, United StatesPosition Summary · SeamonWhiteside is in search of an ambitious and talented professional to serve as a Civil Engineering Project Manager in our growing Summerville, SC office. · The Civil Engineering - Project Manager will continue growing in their role while focusing to further ...
-
MEDICAL DIRECTOR
2 weeks ago
UPHAMS CORNER HEALTH CENTER Dorchester, United StatesJob Details · Job Location · 415 Columbia Rd - Dorchester, MA · Position Type · Full Time 30+ hours · Education Level · Graduate Degree · Travel Percentage · Negligible · Job Shift · Day · Job Category · Health Care · Description · Title: Medical Director - Primary Care · Departm ...
-
INVENTORY CONTROL ANALYST- 1st Shift
4 weeks ago
Thorne Research Summerville, United StatesINVENTORY CONTROL ANALYST- 1st shift - 5am-3:30pm Monday-Thursday or Wednesday-Saturday Subject to change · POSITION SUMMARY: The Production Inventory Control Analyst is responsible for the daily input and monitoring of production materials inventory in accordance with the Compan ...
-
Thorne Research Inc Summerville, United StatesJob Description · Job DescriptionThe Department of Defense (DOD) manages the DOD SkillBridge Program, an opportunity for active-duty Service Members to gain civilian work experience during their last 180 days of service. DOD SkillBridge connects service members with organizations ...
-
School Psychologist
2 weeks ago
EduServe Summerville, United StatesJob Description · Job Purpose: · The School Psychologist is directly responsible for the psychological assessment of academic, social, emotional, and behavioral domains utilizing problem-solving and standardized evaluations. The School Psychologist monitors the completion of cas ...
-
School Psychologist
2 weeks ago
Charter Schools USA Summerville, United StatesJob Purpose: · The School Psychologist is directly responsible for the psychological assessment of academic, social, emotional, and behavioral domains utilizing problem-solving and standardized evaluations. The School Psychologist monitors the completion of case study evaluations ...
-
Scheduler
2 weeks ago
Thorne Summerville, United StatesAt Thorne we make products that matter - ones that make people's lives better. Each day begins with a mission to help others discover and achieve their best health. We count on our team members to challenge and push the boundaries to make that happen. You'll be joining a team of ...
-
Administrative Assistant
2 weeks ago
Preferred Appliance Sales and Repair - APS Summerville, United StatesJob Description · Job DescriptionBenefits:401(k) matching · Company parties · Competitive salary · Employee discounts · Paid time off · Training & development · **Company:** Preferred Appliance Sales and Repair · **About Us:** · Preferred Appliance Sales and Repair is a thriving ...
Clinical Research Coordinator-Dorchester, MA - Care Access
Description
What We DoCare Access is delivering the future of medicine today Care Access has a revolutionary model that breaks down traditional barriers to clinical trials that limit participation among physicians and patients to 3%.
Who We AreWe care.
Our people are the engines behind our mission:
to revolutionize access to clinical trials for the benefit of patients everywhere. We care for one another, find new ideas to accelerate medicine, and seed a long-term impact for generations.
Position OverviewThe Clinical Research Coordinator's primary responsibilities are to utilize Good Clinical Practices (GCP)s in the process of screening, enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.
What You'll Be Working OnDuties include but not limited to:Patient Coordination:
The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.
Physical and Travel RequirementsWhat You BringKnowledge, Skills, and Abilities:
Certifications/Licenses, Education, and Experience:
Our work brings life-changing therapies to those in need and paves the way for newer and greater treatments to reach the world.
We're proud to advance these breakthroughs and work with the big players while engaging with the best physicians and caring for patients.
Our team of experts is paving the way to take this vision forward through innovation and a unique technology-enabled service model.
We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.
Care Access is unable to sponsor work visas at this time.Employment StatementCare Access complies with all employment laws and regulations with respect to its employment practices, terms and conditions of employment, and pay equity and wages.
Care Access does not engage in any unfair or forced labor practice and does not tolerate, under any circumstances, the use of any form of forced or involuntary labor, child labor, or human trafficking.
This extends to suppliers, partners, or other third parties with whom Care Access does business. Care Access values and promotes the protection of human rights everywhere.