Clinical Research Lead Assistant Job at iconplc (CHICAGO, IL, SEATTLE, WA, HOUSTON, TX, KANSAS CITY, MO, LAS VEGAS, NV)

New

Assistant Clinical Lead – Prosthetics – Roehampton

We have an exciting opportunity for an ambitious Prosthetist to take the next st...

Location

United Kingdom , Roehampton

Salary:

Not provided

AM Healthcare Group

Expiration Date

Until further notice

Requirements

Strong clinical experience within prosthetics and commitment to the highest standard of patient care, with experience in MDT environments.
Excellent communication, interpersonal and leadership skills.
Ability to prioritise, plan, and manage multiple priorities.
Proven experience of working effectively within a team environment with the ability to coach, mentor, and motivate team members.
Evidence of involvement in service development or improvement projects and implementation.
Skilled in communicating complex information to diverse patient groups, including children and individuals with learning disabilities.
Ability to work flexibly, balancing clinical and assigned operational priorities.
Fully proficient with Outlook, Excel, Word and PowerPoint.
BSc (Hons) in Prosthetics and Orthotics or equivalent
HCPC registration

Job Responsibility

Support the Clinical Lead and Operations Manager in the delivery, development, and continuous improvement of clinical services, ensuring high standards of patient care.
Supervise clinical colleagues, and students, and provide coaching, mentorship, and constructive feedback to support professional development.
Support the Clinical Lead and Operations Manager with workforce and service planning by providing clinical insight that informs strategic priorities, ensuring that staffing, resources, and service models align with both patient needs and organisational objectives.
Exercise sound judgement in day-to-day decision-making, balancing individual patient care with service delivery requirements and organisational targets, and adapting quickly when urgent reprioritisation is required.
Support the Clinical Lead and Operations Manager with operational planning, rostering, and resource allocation to maximise efficiency and meet KPIs both individually and as a team.
Deliver high-level clinical care while supporting the team to maintain and develop practical skills in line with prescription guidelines.
Assist with financial planning, forecasting, budget awareness, and cost-effectiveness, including stock monitoring, audits, and waste reduction initiatives.
Provides clinically effective, evidence-based care while supporting the team to maintain quality standards by following prescription guidelines and supporting the Clinical Lead and Operations Manager to embed these within the team.
Proactively lead and support research, audit, and service improvement projects, promoting innovation and evidence-based practice.
Support the Clinical Lead and Operations Manager in overseeing data quality, clinical governance compliance, and effective communication across the team and with external partners.

What we offer

Competitive market salary
Incremental holiday allowance stating at 35 days, increasing to 41 days with length of service (inclusive of bank holidays)
Refer a Friend incentive scheme
Enhanced Family Leave/Pay
Death in Service benefit
Cycle to Work Scheme
Recognition schemes
Continuing professional development

Fulltime

New

Assistant Clinical Lead – Orthotics

We have an exciting opportunity for an ambitious Orthotist to take the next step...

Location

United Kingdom , Roehampton

Salary:

Not provided

AM Healthcare Group

Expiration Date

Until further notice

Requirements

Strong clinical experience within Orthotics and commitment to the highest standard of patient care, with experience in MDT environments
Excellent communication, interpersonal and leadership skills
Ability to prioritise, plan, and manage multiple priorities
Proven experience of working effectively within a team environment with the ability to coach, mentor, and motivate team members
Evidence of involvement in service development or improvement projects and implementation
Skilled in communicating complex information to diverse patient groups, including children and individuals with learning disabilities
Ability to work flexibly, balancing clinical and assigned operational priorities
Fully proficient with Outlook, Excel, Word and PowerPoint
BSc (Hons) in Prosthetics and Orthotics or equivalent
HCPC registration

Job Responsibility

Provide clinical leadership within the paediatric service at St George's Hospital as the lead clinician for Ponseti, Neurodisability, Spina Bifida, and Pectus clinics, undertaking assessment, treatment planning, and patient management
Supervise clinical colleagues, and students, and provide coaching, mentorship, and constructive feedback to support professional development
Work within multidisciplinary teams alongside consultants, surgeons, therapists, nurses, patients, and families to deliver coordinated care
Exercise sound judgement in day-to-day decision-making, balancing individual patient care with service delivery requirements and organisational targets, and adapting quickly when urgent reprioritisation is required
Support the Clinical Lead and Operations Manager with operational planning, rostering, and resource allocation to maximise efficiency and meet KPIs both individually and as a team
Attend surgical planning meetings and case discussions, providing orthotic input and supporting patient care throughout the surgical and rehabilitation pathway
Manage and attend orthotics theatre lists, including providing post-operative casting and orthotic management following surgical procedures
Assist with financial planning, forecasting, budget awareness, and cost-effectiveness, including stock monitoring, audits, and waste reduction initiatives
Provides clinically effective, evidence-based care while supporting the team to maintain quality standards and supporting the Clinical Lead and Operations Manager to embed these within the team
Proactively lead and support research, audit, and service improvement projects, promoting innovation and evidence-based practice

What we offer

Competitive market salary
Incremental holiday allowance stating at 35 days, increasing to 41 days with length of service (inclusive of bank holidays)
Refer a Friend incentive scheme
Enhanced Family Leave/Pay
Death in Service benefit
Cycle to Work Scheme
Recognition schemes
Continuing professional development

Fulltime

Clinical Assistant Lead

The Clinical Assistant is responsible for direct care provided to patients and f...

Location

United States , Chestnut Hill

Salary:

50000.00 - 62853.73 USD / Year

Dana-Farber Cancer Institute

Expiration Date

Until further notice

Requirements

High School Diploma or GED required
college coursework preferred
2 years of equivalent experience in a medical setting
Phlebotomy certification may be preferred based on location (Yawkey 2, Satellites)
BLS Certification required within 60 days of hire

Job Responsibility

Ensures proper patient identification and maintains patient safety, privacy, confidentiality and follows guidelines under HIPAA
Obtains and records vital signs, pain screens, weights and heights accurately into Electronic Medical Records (EMR)
Obtains specimens (urine, stool, sputum, etc.) and ensures accurate labeling in presence of patient
Performs phlebotomy and EKG as applicable and is competent in the two patient identifier practice
May precept with specific training
Assists with disease center specific procedural needs as applicable
Transports patients, medical records, specimens, blood components, equipment and supplies in accordance with Institute policy
Ensures that all patients on schedule are accounted for and communicate with providers/patients and colleagues as to approximate wait times
May be required to assist with research specific patient data entry as required
Assures that all clinical areas have an adequate stock of medical supplies, equipment, and forms

Fulltime

Clinical Assistant Lead

The Clinical Assistant is responsible for direct care provided to patients and f...

Location

United States , Chestnut Hill

Salary:

54772.00 - 68971.50 USD / Year

Dana-Farber Cancer Institute

Expiration Date

Until further notice

Requirements

High School Diploma or GED required
college coursework preferred
Completion of an accredited Medical Assistant Program inclusive of an externship
OR 1 year of experience in a Medical Assistant, Clinical Assistant, Certified Nursing Assistant or related clinical role
OR Nurse Students in an accredited Bachelor’s program with at least 2 completed clinical rotations may be considered
Phlebotomy certification may be preferred based on location
3 years of equivalent experience in a medical setting
BLS Certification required within 60 days of hire

Job Responsibility

Ensures proper patient identification and maintains patient safety, privacy, confidentiality and follows guidelines under HIPAA
Obtains and records vital signs, pain screens, weights and heights accurately into Electronic Medical Records (EMR)
Obtains specimens and ensures accurate labeling
Performs phlebotomy and EKG as applicable
May precept with specific training
Assists with disease center specific procedural needs
Transports patients, medical records, specimens, blood components, equipment and supplies
Ensures that all patients on schedule are accounted for and communicate with providers/patients and colleagues as to approximate wait times
May be required to assist with research specific patient data entry
Assures that all clinical areas have an adequate stock of medical supplies, equipment, and forms

Fulltime

Clinical Research Assistant – MCD Scholar Program

At Boston Children’s Hospital, the quality of our care – and our inclusive hospi...

Location

United States , Boston

Salary:

41246.40 - 61339.20 USD / Year

Boston Children's Hospital

Expiration Date

Until further notice

Requirements

A Bachelor’s Degree is required
Analytical skills to gather and interpret data
Excellent organizational skills and attention to detail
Effective communication and writing skills to provide critical information to team members, patients, and families with ability to triage and escalate concerns to appropriate leadership
Problem-solving, troubleshooting abilities and resourcefulness

Job Responsibility

Clinical Research: Involves subject recruitment, IRB submissions, data analysis, and manuscript preparation
Study Design & Analytics: Exposure to research methodology, statistics, and clinical science study design
Research Ethics: Training in human subjects, protections and management of multicenter registries
Clinical Exposure Scribe Role: Participate in patient visits, documentation, and learn clinical decision-making and physical exam techniques
Shadowing & Mentorship: Collaborate with leading orthopedic surgeons
attend lectures, case reviews, and conferences
Educational Opportunities Daily Lecture Series: Covers orthopedic topics and research skills
Weekly & Quarterly Events: Includes case reviews, journal clubs, and visiting professor seminars
Research Engagement: Opportunities for co-authorship on publications and presentations at regional/national conferences
Mentorship and Scholar Support Mentorship: One-on-one guidance from top faculty, with regular career coaching and project feedback

What we offer

Flexible schedules
Affordable health, vision and dental insurance
Child care and student loan subsidies
Generous levels of time off
403(b) Retirement Savings plan
Pension
Tuition and certain License and Certification Reimbursement
Cell phone plan discounts
Discounted rates on T-passes

Fulltime

New

Clinical Research Coordinator II

Job Description Must have RN licensure to qualify. PURPOSE AND SCOPE: Responsi...

Location

United States , Tupelo

Salary:

Not provided

Fresenius Kidney Care Eupora

Expiration Date

Until further notice

Requirements

Graduate of a technical program in healthcare, specifically as a Registered Nurse
2 to 4 years of nursing experience, specifically as a Registered Nurse
Has successfully performed in the role of Clinical Research Coordinator I for a minimum of 3 years and demonstrated outstanding performance through performance evaluations, certification and other job performance measures
Research experience preferred
Critical care, nephrology and/ or cardiac nursing experience desirable
Willing to pursue CCRC or CCRP certification when eligible
Current state licensure, if applicable
Good computer skills: Microsoft Office minimally
Excellent communication and organizational skills
Ability to work independently, and exhibit diplomacy and problem solving skills in the performance of this role

Job Responsibility

Assists with the determination of the guidelines for the collection of clinical data and coordinates and implements procedures and processes for data collection
Coordinates all aspects of study subject care from pre-screening through study completion as defined by the protocol and Principal Investigator (PI) delegation
Protect the rights and the well-being of subjects enrolled in studies
Ensures thorough, individualized, protocol-based study subject education on all study process requirements including but not limited to: informed consent, study participation obligations, appropriate use of investigational product, safety, privacy, rights and responsibilities
Develops processes for methodically monitoring the status of study subjects as they progress through the study's timeline of activities
Regularly evaluates the study subjects' condition and communicates/documents concerns to PI to ensure subject safety
Accurately documents study subject activities as outlined by the protocol
Maintains documents according to applicable HIPAA and regulatory requirements
Implements study-specific quality goals and practices
Acts as the point of contact or lead person in a facility/practice to oversee protocol compliance

What we offer

Healthcare
Continuing Education
Paid Time Off
Collaborative Environment
Additional Perks
401(k) Retirement Saving

Clinical Research Coordinator II

Responsible for the collection, accuracy and validity of clinical research data ...

Location

United States , Denver

Salary:

59000.00 - 100000.00 USD / Year

Fresenius Kidney Care Eupora

Expiration Date

Until further notice

Requirements

Graduate of a technical program in healthcare, AA in Life Sciences or other health related field
2 to 4 years of clinical research experience, or has successfully performed in the role of Clinical Research Coordinator I for a minimum of 3 years and demonstrated outstanding performance through performance evaluations, certification and other job performance measures
Critical care, nephrology and/ or cardiac nursing experience desirable
Willing to pursue CCRC or CCRP certification when eligible
Current state licensure, if applicable
Good computer skills: Microsoft Office minimally
Excellent communication and organizational skills
Ability to work independently, and exhibit diplomacy and problem solving skills in the performance of this role

Job Responsibility

Assists with the determination of the guidelines for the collection of clinical data and coordinates and implements procedures and processes for data collection
Coordinates all aspects of study subject care from pre-screening through study completion as defined by the protocol and Principal Investigator (PI) delegation
Protect the rights and the well-being of subjects enrolled in studies
Ensures thorough, individualized, protocol-based study subject education on all study process requirements including but not limited to: informed consent, study participation obligations, appropriate use of investigational product, safety, privacy, rights and responsibilities
Develops processes for methodically monitoring the status of study subjects as they progress through the study’s timeline of activities
Regularly evaluates the study subjects’ condition and communicates/documents concerns to PI to ensure subject safety
Accurately documents study subject activities as outlined by the protocol
Maintains documents according to applicable HIPAA and regulatory requirements
Implements study-specific quality goals and practices
Acts as the point of contact or lead person in a facility/practice to oversee protocol compliance

What we offer

Medical insurance
Dental insurance
Vision insurance
401(k) with company match
Paid time off
Parental leave

Fulltime

Animal Health Clinical Research Associate III

At Argenta, we’re more than a company — we’re a global team, dedicated to health...

Location

United States , Shawnee

Salary:

Not provided

Argenta

Expiration Date

Until further notice

Requirements

8+ years clinical trial monitor experience within a Clinical Research Organization or major Animal Health pharmaceutical company
proven experience in GCP late phase clinical trials in animal health
attention to detail and analytically driven
dependability, flexibility and ability to multitask and manage time effectively
Minimum of 8 years’ experience in an animal health research role, Monitor and Clinical Research Associate positions preferred
Experience in Good Clinical Practice (GCP) data management, quality control, and/or quality assurance preferred
Collaborative working style. Lead and motivate people through influence across all levels and functions of the organization
Ability to look for creative solutions to resolve complex issues
Strong technical writing ability
Results oriented and driven

Job Responsibility

Coordinates and conducts GCP and study protocol training at study sites and assures training is documented
Builds rapport with study site staff to assure compliance with the protocol, applicable regulatory and guidance documents, SOPs, and all study activities
Assists in reviewing the study records and all study notebooks to ensure contents are current and complete
Assists in providing tracking and Quality Control (QC) of data as required and assists with responses to QA audits
Evaluates Investigators and assists with selection of appropriate sites to conduct clinical studies
Collaborates with the study Project Manager to assure study sites selected meet the needs of the study protocol
Monitors assigned study sites through review of electronic data capture (EDC) systems, faxed, emailed, and paper documentation
Serves as the liaison between Argenta US Clinical and study site personnel
Facilitates clarifications, corrections, and data query resolution with study sites or data management personnel
Tracks adverse events (AE’s) encountered in clinical studies and ensures all serious AEs and non-serious AEs are documented and communicated appropriately to the Project Manager and Sponsor

What we offer

strong culture
great benefits
opportunity for growth

Fulltime

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Clinical Research Lead Assistant

Job Description

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