Edc Jobs in Usa
28 positions found — Page 2
Highlights:
- Salary: $75,000 - $90,000 based on Exp
- Full Benefits
- Mon - Fri Schedule; fully on on site
- Studies in allergy, asthma, vaccines, and more!
Our Client:
We are working with an exciting clinical trial site organization with over 25 locations, dedicated to advancing innovative therapies and improving lives by making clinical research more efficient and accessible. They focus on on large-volume recruitment and retention of diverse and specialty patient populations, and have an experienced team with extensive physician partnerships help deliver high-quality data across a wide range of therapeutic areas!
The Role:
We are seeking an experienced CRC that values strong operations, thoughtful study execution, and team-based approach to clinical research!
- Coordinate all aspects of assigned clinical trials from site initiation through close-out
- Conduct subject visits and ensure accurate, timely documentation in compliance with all applicable standards
- Maintain compliance with protocols, GCP/ICH guidelines, FDA regulations, IRB requirements, and SOPs
- Manage subject recruitment, informed consent, and retention activities (There is a recruitment team to support day to day recruitment)
- Ensure timely EDC data entry and resolution of queries
- Report and follow up on AEs, SAEs, and protocol deviations
- Collaborate with investigators, sponsors/CROs, labs, and internal teams
- Prepare for and participate in monitoring visits, audits, and inspections
- Maintain regulatory documentation and ensure training compliance for amendments and systems
- Perform study procedures such as phlebotomy, ECGs, and sample processing (as trained)
- Attend investigator meetings and provide cross-functional support as needed
- Maintain working knowledge of protocols, lab manuals, equipment calibration, and inventory
Requirements:
- 3+ years exp as a CRC on sponsor backed trials
- Ability to work on site M-F (NO hybrid or remote days)
Senior Clinical Research Coordinator Opportunity in Miami, FL (33155)
Position Summary
The Clinical Research Coordinator plays an integral role in supporting the day-to-day operations of clinical trials at the investigator site. This position is responsible for planning, coordinating, and executing clinical studies in compliance with study protocols, contracted scope of work, ICH/GCP guidelines, sponsor and CRO requirements, and applicable local regulations.
Duties/Responsibilities
- Coordinate study startup activities, including site selection visits, source documentation setup, recruitment planning, and site preparation.
- Lead weekly site meetings and collaborate with site leadership to address facility and operational needs.
- Manage investigator signature processes and support subject recruitment, enrollment, and contingency planning.
- Monitor and track screening, enrollment, and study milestones, identifying barriers and implementing solutions.
- Partner with recruitment teams to improve enrollment for difficult-to-fill studies.
- Ensure timely and accurate data entry in EDC and clinical trial management systems, addressing discrepancies as needed.
- Participate in study initiation, monitoring, and close-out visits, including reviewing monitor reports and following up on action items.
- Conduct quality checks on subject visits and collaborate with compliance teams to address issues.
- Work with source documentation staff to ensure readiness for patient visits.
- Provide training, mentorship, and troubleshooting support to site staff; assist with onboarding new employees and evaluating training progress.
- Act as a liaison between site operations, financial teams, and leadership to improve workflows and communication.
- Develop and maintain strong investigator and sponsor relationships while providing progress updates.
- Participate in staff evaluations, candidate interviews, and employee development activities.
- Deliver presentations at training events and contribute to external collaborations for specialized study protocols.
- Support SOP development, special projects, business development initiatives, and team-building activities.
- Perform other duties as assigned.
Required Skills/Abilities
- Strong knowledge of medical terminology, ICH/GCP, and regulatory requirements.
- Excellent interpersonal, communication, and organizational skills.
- Proficiency with Microsoft Office, including Excel.
- Bilingual in English and Spanish, with strong written and verbal skills.
- Ability to work independently and collaboratively within a team.
- Strong problem-solving skills with the ability to maintain confidentiality and build effective working relationships.
Education/Experience
- Bachelor's Degree Required
- Minimum 4+ years of clinical research coordinator experience, preferably with industry-sponsored trials.
Additional Details
- Location: Miami, FL (33155)
- Position: Senior Clinical Research Coordinator
- Employment: ~6 month (1,040 Hours) contracted probationary period into direct hire / permanent position
- Hours: Monday-Friday; 8:30AM-5PM; Onsite 5 Days a Week
- Pay Range: $66,000-$89,000 Annual Salary (Dependent on background and years of experience)
- Requirements: 4+ Years of Clinical Research Coordinating Experience; Bachelor's Degree Required
Location: Onsite – Pennington, NJ Hybrid
Step into a high-impact role where your work directly shapes the future of innovative therapies for rare and serious diseases. My client is advancing a cutting-edge clinical pipeline, and this role sits at the center of translating bold science into meaningful patient outcomes. You’ll lead complex global trials while influencing how clinical operations scale and evolve.
Why You Should Apply
- Drive end-to-end clinical trials that can redefine standards of care
- Play a visible role partnering with senior leadership and key stakeholders
- Lead CROs, vendors, and cross-functional teams with real decision-making authority
- Contribute to building systems, SOPs, and operational excellence from the ground up
- Competitive salary range and bonus!
- Comprehensive benefits and growth-focused environment
- Lead clinical trials from protocol development through closeout
- Own project plans, timelines, budgets, and risk mitigation strategies
- Manage CROs, vendors, sites, and investigator relationships
- Ensure inspection readiness, regulatory compliance, and data integrity
- Optimize patient recruitment, retention, and operational performance
- Provide mentorship and leadership across clinical teams
- Bachelor’s degree in life sciences, pharmacy, nursing, or related field (advanced degree preferred)
- Strong knowledge of GCP, ICH, FDA, and EMA requirements
- Expertise with CTMS, EDC, and clinical trial systems
- Financial and vendor management acumen
- Confident leader in fast-paced, multi-study environments
We’d love to see your resume, but we don’t need it to have a conversation. Send us an email to and tell me why you’re interested. Or, feel free to email your resume. Please include Job#19719.
With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders.
Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society.
Job Summary The Clinical Study Manager is responsible for the delivery and execution of global clinical studies under the direction of a Study Delivery Lead.
This role is primarily focused on tactical study delivery and reports to a Director or higher-level position.
The position requires excellent written and verbal communication, project management skills, and attention to detail.
The Clinical Study Manager will have routine interaction with key internal and external stakeholders to communicate project status, resolve issues, and troubleshoot routine inquiries.
This position may require the Clinical Study Manager to take on a dual role of both operational strategy and study execution.
Job Description Responsibilities Clinical Operations Study Management(Global) has primary accountability for operational execution and delivery of assigned clinical trials, including study level time, cost and quality deliverables.
In a CRO outsourcing model, responsibilities also include: Study Oversight: Lead the clinical study operational aspects of planning, execution, and management of one or more Phase 1-3 clinical trials.
May provide support as back-up to the Study Delivery Lead as needed.
Cross-Functional Leadership: Participate and provide expertise as a cross-functional study team member, including vendors, and liaise with other departments.
Provide mentorship of more junior Operations team members.
Vendor Management: Lead vendor selection, contracting, and management to maintain study quality and compliance and adherence to scope of work within timelines and budget.
Oversee complex vendors (i.e., eCOA).
CRO Oversight: Responsible for the oversight, performance, and management of CRO(s) and 3rd party vendors (sub-contracted by CRO) to ensure compliance with Daiichi Sankyo’s quality measures and adherence to scope of work within timelines and budget at a task level.
Coordinate and develop materials for CRO KOMs and Investigator meetings.
Compliance and Regulatory: Ensure compliance with GCP/ICH guidelines and other regulatory requirements (FDA, MHRA, etc.).
Timeline and Budget Management: Create and coordinate clinical study timelines and budgets with Global Project Management and R&D Finance to meet critical milestones and manage budgets.
Responsible for continual review of study timelines and study budget.
Risk Management: Identify, mitigate, and escalate risks per process throughout the study lifecycle.
Ensure risks are appropriately logged in the risk management system.
Study Material Development: Co-develop and manage study materials, including training materials, protocols, CRFs, and study operational plans.
Ensure all necessary operational materials are in place.
Data Cleaning: Oversee site and monitor data cleaning metrics including EDC data entry, query resolution timeliness, and protocol deviation review.
Site Management: Oversee site selection, start-up, monitoring, and closeout for the trial.
Study Communication: Triage, resolve or escalate study issues /risk mitigations to the Study Delivery Lead.
Support all inspection readiness and quality initiatives pertaining to assigned stud(ies).).
oSupports risk Management initiatives oSupports audit/inspection activities as needed oEnsures trial master file is complete and accurate for assigned stud(ies) Communication and Reporting: Provide regular updates on study progress to key stakeholders.
Training: Identify training needs for key stakeholders as needed, e.g., study team members, vendors and ensure training is carried out.
Develop training materials as necessary.
Responsibilities Continued Qualifications Education Qualifications Bachelor's Degree preferred in Life Sciences required Experience Qualifications 3 or more years required and Relevant experience is required with a BSc required and Experience in oversight of global clinical trials (all phases) in all stages of delivery with requisite industry training and experience required and Experience considered relevant includes clinical or basic research in a Pharmaceutical company, a Medical device/Diagnostic company, Academic Research Organization (ARO) or Contract Research Organization (CRO).
preferred CRA experience preferred Time spent directly in a medical environment (e.g.
as a Study Site Coordinator) preferred Familiarity to a Japan-based organization preferred Travel Requirements Ability to travel up to 10% of the time.
In-house office position that may require occasional travel (domestic or global).
Additional Information Daiichi Sankyo, Inc.
is an equal opportunity/affirmative action employer.
Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.
Salary Range: USD$133,600.00
- USD$200,400.00 Download Our Benefits Summary PDF
Position Summary:
The Plumber installs and repairs plumbing fixtures, equipment and systems in accordance with regulations and safety standards.
Essential Duties:
- Installs and repairs equipment and fixtures, including toilets, sinks, drains, gas/water lines, dishwashers, water coolers and water heaters.
- Routes and cuts openings to accommodate installation or repair of equipment and fixtures and ease of maintenance.
- Performs preventative maintenance by inspecting fixtures and making necessary repairs.
- Repairs and maintains water supply, irrigation and sewage systems.
- Certifies backflow devices and repair or install as required by code or standards.
- Works rom building plans, blueprints and sketches to plan and layout routing and placement.
- Organizes the job site ensuring it is properly staffed and has the necessary equipment.
- Coordinates with other tradespersons completing projects when necessary.
- Required to have prompt, regular attendance in-person and be available to work on-site, in-person during regular business hours and as needed.
- Performs other duties as assigned by an appropriate administrator or their representative.
Knowledge, Skills, & Abilities:
- Written and oral communication.
- Computer skills.
- Proficient in the installation and repair of all infrastructure plumbing lines and associated equipment such as, but not limited to, water and sewer lines, water fountains, lavatories, urinals.
- Ability to correctly and safely operate all tools.
Minimum Requirements:
EDUCATION:
• High School Diploma or GED required.
CERTIFICATION/LICENSE:
• Valid Georgia driver’s license.
• Must comply with Transportation Regulation EDC-R.
• Valid Plumber’s License.
• Requirements within 1 year of employment date: Must obtain backflow certification within one year of employment.
WORK EXPERIENCE:
• 3 years of related work experience.
Salary Grade: 121
Salary Range: Salary Schedules - Atlanta Public Schools
Work Year: Annual
Physical Abilities and Working Conditions
The physical abilities, working conditions and other conditions of employment listed in this document are representative of, but are not intended to provide an exhaustive list of the requirements for positions in this classification. In the event of an emergency or situation requiring guidance from Federal, State, or local or school district authorities, the requirements of this position may change temporarily or for the school year to best serve the needs of our students.
Vision: Ability to read small print and view a computer screen for prolonged periods.
Hearing: Ability to tolerate exposure to noisy conditions.
Speech: Ability to be understood in face-to-face communications, to speak with a level of proficiency and volume to be understood over a telephone or computer.
Upper Body Mobility: Ability to use hands to grasp, and manipulate small objects; manipulate fingers, twist and bend at wrist and elbow; extend arms to reach outward and upward; use hands and arms to lift objects; turn, raise, and lower head. Strength: Ability to lift, push, pull and/or carry objects which weigh as much as 5 or more pounds on a frequent basis. Incumbent may be required to physically restrain parties involved in a conflict.
Environmental Requirements: Ability to encounter constant work interruptions; work cooperatively with others; work independently; work indoors.
Mental Requirements: Ability to read, write, understand, interpret and apply information at a moderately complex level essential for successful job performance; math skills at a high school proficiency level; judgement and the ability to process information quickly; learn quickly and follow verbal procedures and standards; give verbal instruction; rank tasks in order of importance; copy, compare, compile and coordinate information and records. Understand how to manage stress.
Remote Work Requirements:
Additional Work Conditions & Physical Abilities: Ability to be flexible and adapt as needed between various in-person working environments.
The Atlanta Public School System does not discriminate on the basis of race, color, religion, sex,citizenship, ethnic or national origin, age, disability, medical status, military status, veteran status, marital status, sexual orientation, gender identity or expression, genetic information, ancestry, or any legally protected status in any of its employment practices, educational programs, services or activities. Reasonable accommodations may be made to enable individuals with disabilities to perform essential duties.
This job description is intended to accurately reflect the duties, responsibilities and requirements of the position. It is not intended to be and should not be construed as an all-inclusive list of all the responsibilities, skills, or working conditions associated with the position. Management and administration reserves the right to modify, add, or remove duties and assign other duties as necessary.
Group Therapist
EDC - Pennsylvania
Villanova, PA
Monte Nido Philadelphia Day Treatment, located in Villanova, PA is a primary eating disorder day treatment program for adults and adolescents seeking treatment for Anorexia Nervosa, Bulimia Nervosa, Binge Eating Disorder, or Exercise Addiction. Through partial hospitalization and intensive outpatient programming, clients participate in group and individual therapy, benefit from Monte Nido’s clinical, medical, psychiatric and nutritional expertise and experience real life challenges.
We are seeking a Group Therapist to join our Clinical Team.
#LI-ONSITE
Total Rewards::
Discover a rewarding career with us and enjoy an array of comprehensive benefits! We prioritize your success and well-being, providing:
- Competitive compensation
- Medical, dental, and vision insurance coverage (Benefits At a Glance)
- Retirement
- Company-paid life insurance, AD&D, and short-term disability
- Employee Assistance Program (EAP)
- Flexible Spending Account (FSA)
- Health Savings Account (HSA)
- Paid time off
- Professional development
- And many more!
We are committed to creating a diverse environment and are proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.
Responsibilities Include::Facilitate therapy groups
Provides some individual or family therapy
Model normalized eating habits by eating meals to completion when working during mealtimes
Contribute to maintaining a safe and recovery-minded milieu
Participate as needed in discharge and after-care planning
Provides safe, empathetic, and affirming care for each client and their unique circumstance based on the clients' intersecting identities
Master’s degree, at minimum, in clinical counseling or related discipline.
Licensed (or license-eligible) in a counseling field (e.g., Psychologist, LMFT, LCSW, etc.).
Prior experience treating those with eating disorders in a residential or inpatient setting is very helpful.
Knowledge of diversity, equity and inclusion practices
#montenido
Join a Growing Clinical Research Team in Miami
We are seeking an experienced and driven Clinical Research Coordinator (CRC) who is passionate about advancing medicine and providing exceptional patient care. If you thrive in a fast-paced research environment, understand regulatory compliance, and enjoy working directly with patients, this opportunity is for you.
As a key member of our research team, you will play an essential role in ensuring clinical trials are conducted efficiently, ethically, and in full compliance with regulatory standards.
What You'll Do
- Coordinate and oversee daily clinical trial operations
- Recruit, screen, and enroll study participants
- Obtain informed consent and maintain accurate source documentation
- Ensure compliance with study protocols, GCP, and FDA regulations
- Ensure protocol comprehension and adherence
- Schedule and conduct study visits
- Perform phlebotomy and process laboratory specimens as required
- Enter and manage data in EDC systems with accuracy and timeliness
- Communicate effectively with sponsors, CROs, and investigators
- Prepare for and support monitoring visits and audits
What We're Looking For
Required:
- Prior experience as a Clinical Research Coordinator
- Bilingual (English/Spanish) — required
- Phlebotomy skills
- Strong understanding of GCP and FDA regulations
- Excellent organizational and communication skills
- Ability to manage multiple studies simultaneously
- Experience in EDC systems
Preferred:
- Bachelor’s degree in Biology, Nursing, Health Sciences, or related field.
Why Join Us:
- Competitive pay: $23–$28/hour
- Collaborative and supportive team environment
- Opportunity to contribute to meaningful clinical research
- Professional growth within a dynamic research setting
Ready to Play:
If you meet the qualifications and are ready to make an impact in clinical research, we encourage you to apply today. We are looking to hire promptly and will be reviewing applications on a rolling basis.
Physician Assistant ? Clinical Research (Sub-Investigator)
Location: Brooklyn, NY
About Brooklyn Clinical Research:
Brooklyn Clinical Research was founded to increase access to clinical trials for underrepresented populations. Clinical-trial enrollment should accurately represent the broader population. In meeting this objective, we help improve therapeutic efficacy and safety for all individuals.
Position Overview:
We are seeking a clinically adept, highly motivated Physician Assistant to join our growing research team as a Sub-Investigator. This is a hands-on clinical research role, working alongside our full-time Principal Investigator (MD) to conduct industry-sponsored clinical trials.
The ideal candidate will thrive in a fast-paced, dynamic environment where flexibility, strong clinical decision-making, and attention to detail are essential. You will receive full training in clinical research and GCP, and you will play a key role in the daily conduct of clinical trials ? performing protocol-specific assessments, managing study visits, and ensuring participant safety and regulatory compliance.
Key Responsibilities:
- Serve as a Sub-Investigator on assigned clinical trials under supervision of the Principal Investigator.
- Perform protocol-required medical evaluations, including detailed histories, physical exams, safety assessments, and medical oversight of study participants.
- Administer investigational products (e.g., vaccines, injectables) according to protocol.
- Perform and oversee clinical procedures including phlebotomy, vital signs, ECGs, and other protocol-specified tests.
- Assess and document adverse events and serious adverse events according to FDA and Sponsor guidelines.
- Maintain thorough, timely, and accurate source documentation and electronic data entry (EDC, eSource, CTMS).
- Collaborate closely with clinical coordinators, regulatory staff, sponsors, and CROs.
- Participate in monitoring visits, audits, and inspections.
- Maintain comprehensive knowledge of study protocols, informed consent documents, and regulatory requirements.
- Participate actively in team meetings, contributing to ongoing process improvement as our site grows.
Qualifications:
- Graduate of an accredited Physician Assistant program (required).
- Active Physician Assistant license in New York State (required).
- Prior clinical research experience is a strong plus but not required ? training will be provided.
- Current BLS/CPR certification.
Key Attributes for Success:
- Excited to work in a fast-paced clinical environment where protocols and patient needs can vary daily.
- Strong clinical acumen and independent judgment.
- Detail-oriented with excellent documentation skills.
- Highly organized with the ability to manage multiple protocols simultaneously.
- Excellent communication and teamwork skills.
- Commitment to patient safety, protocol adherence, and research integrity.
- Spanish fluency or medical Spanish is a plus but not required.
Position Details:
- Full-time, salaried position, Monday?Friday. Occasional weekend work may be required during high-volume vaccine periods.
- Anticipated Start Date: Late July or Early August 2025
- Salary Range: $140,000 to $170,000 depending on experience.
Why Join Us:
This is an excellent opportunity for a PA who is interested in advancing their career into clinical research while maintaining direct patient interaction. You will be a key member of a high-performing, mission-driven team with meaningful opportunities for professional growth as our research site expands.
Job Type: Full-time
Pay: $140,000.00 - $170,000.00 per year
Benefits:
- 401(k)
- 401(k) matching
- Dental insurance
- Health insurance
- Paid time off
- Vision insurance
Medical Specialty:
- Addiction Medicine
- Emergency Medicine
- Endocrinology
- Hospital Medicine
- Infectious Disease
- Internal Medicine
- Interventional Cardiology
- Neurology
- Pain Medicine
- Primary Care
- Urgent Care
Schedule:
- Monday to Friday
- No nights
License/Certification:
- New York State Physician Assistant License? (Required)
Ability to Commute:
- Brooklyn, NY 11226 (Required)
Work Location: In person
