OBJECTIVE The Clinical Supervisor will be able to use knowledge of clinical interventions and ... Provide disciplinary action as needed for supervisees. * Assist in the development of staff ...
Quick apply
OBJECTIVE The Clinical Supervisor will be able to use knowledge of clinical interventions and ... Provide disciplinary action as needed for supervisees. * Assist in the development of staff ...
Quick apply
OBJECTIVE The Clinical Supervisor will be able to use knowledge of clinical interventions and ... Provide disciplinary action as needed for supervisees. * Assist in the development of staff ...
OBJECTIVE The Clinical Supervisor will be able to use knowledge of clinical interventions and ... Provide disciplinary action as needed for supervisees. * Assist in the development of staff ...
Quick apply
OBJECTIVE The Clinical Supervisor will be able to use knowledge of clinical interventions and ... Provide disciplinary action as needed for supervisees. * Assist in the development of staff ...
Indianapolis, IN · On-site
What we do helps make lives better by advancing novel technologies and medicines, speeding up clinical development timelines and reducing costs. Within PRD, Synthetic Molecule Design and Development ...
Indianapolis, IN · On-site
What we do helps make lives better by advancing novel technologies and medicines, speeding up clinical development timelines and reducing costs. Within PRD, Synthetic Molecule Design and Development ...
Indianapolis, IN · On-site
What we do helps make lives better by advancing novel technologies and medicines, speeding up clinical development timelines and reducing costs. Within PRD, Synthetic Molecule Design and Development ...
Indianapolis, IN · On-site
What we do helps make lives better by advancing novel technologies and medicines, speeding up clinical development timelines and reducing costs. Within PRD, Synthetic Molecule Design and Development ...
Your Role: R&D Quality Assurance Auditor As an R&D Quality Assurance Auditor, you will be part of ... Plan, conduct, and report Quality oversight and audit activities for veterinary Good Clinical ...
Your Role: R&D Quality Assurance Auditor As an R&D Quality Assurance Auditor, you will be part of ... Plan, conduct, and report Quality oversight and audit activities for veterinary Good Clinical ...
Your Role: R&D Quality Assurance Auditor As an R&D Quality Assurance Auditor, you will be part of ... Plan, conduct, and report Quality oversight and audit activities for veterinary Good Clinical ...
Your Role: R&D Quality Assurance Auditor As an R&D Quality Assurance Auditor, you will be part of ... Plan, conduct, and report Quality oversight and audit activities for veterinary Good Clinical ...
Indianapolis, IN · On-site +1
$250/hr
This role is ideal for supervisors who can provide clear feedback, ethical guidance, and practical support in day-to-day clinical development. Gotham's Find a Supervisor feature helps clinicians ...
Indianapolis, IN · On-site +1
$250/hr
This role is ideal for supervisors who can provide clear feedback, ethical guidance, and practical support in day-to-day clinical development. Gotham's Find a Supervisor feature helps clinicians ...
Indianapolis, IN · On-site
$250/hr
This role is ideal for supervisors who can provide clear feedback, ethical guidance, and practical support in day-to-day clinical development. Gotham's Find a Supervisor feature helps clinicians ...
Indianapolis, IN · On-site
$250/hr
This role is ideal for supervisors who can provide clear feedback, ethical guidance, and practical support in day-to-day clinical development. Gotham's Find a Supervisor feature helps clinicians ...
The Translational Sciences group within Lilly Oncology is responsible for bridging mechanistic discovery and clinical development, driving biomarker strategy, combination rationale, resistance ...
The Translational Sciences group within Lilly Oncology is responsible for bridging mechanistic discovery and clinical development, driving biomarker strategy, combination rationale, resistance ...
The Translational Sciences group within Lilly Oncology is responsible for bridging mechanistic discovery and clinical development, driving biomarker strategy, combination rationale, resistance ...
The Translational Sciences group within Lilly Oncology is responsible for bridging mechanistic discovery and clinical development, driving biomarker strategy, combination rationale, resistance ...
Partner with senior leaders across Clinical Development, Regulatory Affairs, Manufacturing & Quality, Patient Safety, Commercial, Policy, and Legal to shape regulatory strategies for the vaccines and ...
Partner with senior leaders across Clinical Development, Regulatory Affairs, Manufacturing & Quality, Patient Safety, Commercial, Policy, and Legal to shape regulatory strategies for the vaccines and ...
Indianapolis, IN · On-site
$133K - $181K/yr
Partner with senior leaders across Clinical Development, Regulatory Affairs, Manufacturing & Quality, Patient Safety, Commercial, Policy, and Legal to shape regulatory strategies for the vaccines and ...
Indianapolis, IN · On-site
$133K - $181K/yr
Partner with senior leaders across Clinical Development, Regulatory Affairs, Manufacturing & Quality, Patient Safety, Commercial, Policy, and Legal to shape regulatory strategies for the vaccines and ...
Indianapolis, IN · On-site
Responsible for overseeing all transactions across all stages of development (discovery, preclinical, clinical, commercial, etc.), including negotiations for business deals, licensing agreements ...
Indianapolis, IN · On-site
Responsible for overseeing all transactions across all stages of development (discovery, preclinical, clinical, commercial, etc.), including negotiations for business deals, licensing agreements ...
Indianapolis, IN · On-site
$143K - $189K/yr
Knowledge of global CMC regulatory requirements and guidelines for synthetic peptides and oligonucleotides to support clinical development, global product registrations, and lifecycle management of ...
Indianapolis, IN · On-site
$143K - $189K/yr
Knowledge of global CMC regulatory requirements and guidelines for synthetic peptides and oligonucleotides to support clinical development, global product registrations, and lifecycle management of ...
Knowledge of global CMC regulatory requirements and guidelines for synthetic peptides and oligonucleotides to support clinical development, global product registrations, and lifecycle management of ...
Knowledge of global CMC regulatory requirements and guidelines for synthetic peptides and oligonucleotides to support clinical development, global product registrations, and lifecycle management of ...
Registered Nurse Clinical Development NICU Your future role at a glance Location: Indianapolis, IN Facility: Ascension St. Vincent Indianapolis Department/Specialty: Clinical Professional Development ...
Registered Nurse Clinical Development NICU Your future role at a glance Location: Indianapolis, IN Facility: Ascension St. Vincent Indianapolis Department/Specialty: Clinical Professional Development ...
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers ... What the Early Phase Business Development Department does at Worldwide The Early Phase Business ...
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers ... What the Early Phase Business Development Department does at Worldwide The Early Phase Business ...
Director for Late Phase clinical trials, responsible for leading and executing the business development strategy focused on Phase II - IV stages of clinical trials. This role requires a strategic ...
Quick apply
Director for Late Phase clinical trials, responsible for leading and executing the business development strategy focused on Phase II - IV stages of clinical trials. This role requires a strategic ...
Director for Late Phase clinical trials, responsible for leading and executing the business development strategy focused on Phase II - IV stages of clinical trials. This role requires a strategic ...
Quick apply
Director for Late Phase clinical trials, responsible for leading and executing the business development strategy focused on Phase II - IV stages of clinical trials. This role requires a strategic ...
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers ... Development department is a group of highly dedicated individuals working as one to bring the best ...
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers ... Development department is a group of highly dedicated individuals working as one to bring the best ...
$17 is the 25th percentile. Wages below this are outliers.
$13.72 - $20.27
50% of jobs
$20.27 - $26.83
4% of jobs
$30.66 is the 75th percentile. Wages above this are outliers.
$26.83 - $33.38
36% of jobs
$33.38 - $39.93
0% of jobs
$39.93 - $46.48
0% of jobs
$46.48 - $53.03
0% of jobs
$53.03 - $59.58
0% of jobs
$59.58 - $66.13
0% of jobs
$66.13 - $72.68
0% of jobs
$72.68 - $79.23
0% of jobs
$79.23 - $85.78
10% of jobs
$13
$32
$85
| Aspect | Clinical Development | Clinical Research Coordinator |
|---|---|---|
| Required Credentials | Bachelor's degree, often advanced degrees in life sciences or related fields; certifications like CCRP or RAC | Bachelor's degree in health sciences or related field; certifications like CCRP beneficial |
| Work Environment | Pharmaceutical or biotech companies, clinical trial teams, R&D departments | Clinical trial sites, hospitals, research centers |
| Employer & Industry Usage | Used in pharmaceutical, biotech, and medical device industries during drug development phases | Used in hospitals, research institutions, and clinical trial sites for managing patient studies |
While both roles are involved in clinical trials, Clinical Development focuses on designing and managing the overall drug development process, whereas Clinical Research Coordinators handle the day-to-day operations at trial sites, ensuring protocol adherence and patient coordination.
Schererville, IN • On-site
Full-time
Re-posted 17 days ago
Individual and Family Therapy PLLC is a group private practice located in Homewood, IL and Matteson, IL. We are looking to expand our team with a Clinical Supervisor who is a self-starter, organized, and genuinely passionate about helping clients and other clinicians.
JOB DESCRIPTION
OBJECTIVE
The Clinical Supervisor will be able to use knowledge of clinical interventions and supervisory skills to aid the clinical team in meeting the company’s goal of providing quality therapeutic care to clients. This is an eclectic role with many potential growth areas, so we are looking for a Clinical Supervisor who will be able to join the team and contribute where needed.
ESSENTIAL FUNCTIONS AND RESPONSIBILITIES
Requirements: