... formulation development, clinical pharmacology, clinical trials, and commercial product ... An excellent opportunity for a Principal Investigator/ Medical Director to join Quotient Sciences ...
... formulation development, clinical pharmacology, clinical trials, and commercial product ... An excellent opportunity for a Principal Investigator/ Medical Director to join Quotient Sciences ...
Director of Product Development Department: Product Marketing, Strategy & Innovation Position ... re-formulation opportunities. Cross-Functional Collaboration * Partner closely with: * Senior ...
Quick apply
Director of Product Development Department: Product Marketing, Strategy & Innovation Position ... re-formulation opportunities. Cross-Functional Collaboration * Partner closely with: * Senior ...
Director of Product Development Department: Product Marketing, Strategy & Innovation Position ... re-formulation opportunities. Cross-Functional Collaboration * Partner closely with: * Senior ...
Director of Product Development Department: Product Marketing, Strategy & Innovation Position ... re-formulation opportunities. Cross-Functional Collaboration * Partner closely with: * Senior ...
Director of Product Development Department: Product Marketing, Strategy & Innovation Position ... re-formulation opportunities. Cross-Functional Collaboration * Partner closely with: * Senior ...
Director of Product Development Department: Product Marketing, Strategy & Innovation Position ... re-formulation opportunities. Cross-Functional Collaboration * Partner closely with: * Senior ...
Director of Product Development Department: Product Marketing, Strategy & Innovation Position ... re-formulation opportunities. Cross-Functional Collaboration * Partner closely with: * Senior ...
Quick apply
Director of Product Development Department: Product Marketing, Strategy & Innovation Position ... re-formulation opportunities. Cross-Functional Collaboration * Partner closely with: * Senior ...
R&D Chemist
Brooksville, FL · On-site
This role is execution-driven--focused on formulation, testing, troubleshooting, and scale-up support. The Technical Director sets R&D strategy; this position drives the technical execution that ...
R&D Chemist
Brooksville, FL · On-site
This role is execution-driven--focused on formulation, testing, troubleshooting, and scale-up support. The Technical Director sets R&D strategy; this position drives the technical execution that ...
Staff Director
Jacksonville, FL · On-site
Lead employees using a performance management and development process that provides an overall ... off, telecommuting, cover for absenteeism, and overtime scheduling. * Maintain transparent ...
Staff Director
Jacksonville, FL · On-site
Lead employees using a performance management and development process that provides an overall ... off, telecommuting, cover for absenteeism, and overtime scheduling. * Maintain transparent ...
Staff Director
Jacksonville, FL · On-site
Lead employees using a performance management and development process that provides an overall ... off, telecommuting, cover for absenteeism, and overtime scheduling. * Maintain transparent ...
Staff Director
Jacksonville, FL · On-site
Lead employees using a performance management and development process that provides an overall ... off, telecommuting, cover for absenteeism, and overtime scheduling. * Maintain transparent ...
Participates as a member of the hospital's management team in planning, policy formulation, and ... Utilizes capabilities of nursing and paraprofessional personnel in the development of orientation ...
Participates as a member of the hospital's management team in planning, policy formulation, and ... Utilizes capabilities of nursing and paraprofessional personnel in the development of orientation ...
Participates as a member of the hospital's management team in planning, policy formulation, and ... Utilizes capabilities of nursing and paraprofessional personnel in the development of orientation ...
Participates as a member of the hospital's management team in planning, policy formulation, and ... Utilizes capabilities of nursing and paraprofessional personnel in the development of orientation ...
Participates as a member of the hospital's management team in planning, policy formulation, and ... Utilizes capabilities of nursing and paraprofessional personnel in the development of orientation ...
Participates as a member of the hospital's management team in planning, policy formulation, and ... Utilizes capabilities of nursing and paraprofessional personnel in the development of orientation ...
Responsible for development of digital first products supporting the needs and risks of USAA ... support formulation of product strategy and enhance competitive intelligence. * Develop and ...
Responsible for development of digital first products supporting the needs and risks of USAA ... support formulation of product strategy and enhance competitive intelligence. * Develop and ...
Director of Nursing
$90K - $95K/yr
Participates as a member of the hospital's management team in planning, policy formulation, and ... Utilizes capabilities of nursing and paraprofessional personnel in the development of orientation ...
Director of Nursing
$90K - $95K/yr
Participates as a member of the hospital's management team in planning, policy formulation, and ... Utilizes capabilities of nursing and paraprofessional personnel in the development of orientation ...
Director of Nursing
$90K - $95K/yr
Participates as a member of the hospital's management team in planning, policy formulation, and ... Utilizes capabilities of nursing and paraprofessional personnel in the development of orientation ...
Director of Nursing
$90K - $95K/yr
Participates as a member of the hospital's management team in planning, policy formulation, and ... Utilizes capabilities of nursing and paraprofessional personnel in the development of orientation ...
The Role * Responsible for conducting pre-formulation, formulation preparation, testing and ... direct pharmaceutical drug product development experience preferred or; AS in Pharmacy ...
The Role * Responsible for conducting pre-formulation, formulation preparation, testing and ... direct pharmaceutical drug product development experience preferred or; AS in Pharmacy ...
The Role * Responsible for conducting pre-formulation, formulation preparation, testing and ... direct pharmaceutical drug product development experience preferred or; AS in Pharmacy ...
The Role * Responsible for conducting pre-formulation, formulation preparation, testing and ... direct pharmaceutical drug product development experience preferred or; AS in Pharmacy ...
Lead and coordinate proposal development and negotiation efforts by partnering closely with ... Small molecule and formulation experience is advantageous. * Understanding of oral solid dose and ...
Lead and coordinate proposal development and negotiation efforts by partnering closely with ... Small molecule and formulation experience is advantageous. * Understanding of oral solid dose and ...
Screening Manager
Miami, FL · On-site
... formulation development, clinical pharmacology, clinical trials, and commercial product ... Provides encouragement, support, positive reinforcement and job enrichment opportunities to direct ...
Screening Manager
Miami, FL · On-site
... formulation development, clinical pharmacology, clinical trials, and commercial product ... Provides encouragement, support, positive reinforcement and job enrichment opportunities to direct ...
Provide direct oversight and management, and coaching and development to the business lending ... the formulation, development, implementation, and administration of Credit Union strategies ...
Provide direct oversight and management, and coaching and development to the business lending ... the formulation, development, implementation, and administration of Credit Union strategies ...
... Development & Regulatory Director. Communicate regularly with President and associated Supervisor/Manager, provide detailed up-to-date reports on current and new formulation, materials ...
... Development & Regulatory Director. Communicate regularly with President and associated Supervisor/Manager, provide detailed up-to-date reports on current and new formulation, materials ...
Telecommute Director Formulation Development information
How does a Telecommute Director of Formulation Development typically collaborate with cross-functional teams while working remotely?
A Telecommute Director of Formulation Development leverages digital collaboration tools to coordinate with R&D, regulatory, manufacturing, and quality assurance teams. Regular virtual meetings, project management platforms, and shared documentation ensure seamless communication and progress tracking. Despite working remotely, directors are expected to proactively facilitate brainstorming sessions, resolve issues in real time, and maintain clear communication channels to drive project milestones. Building strong relationships and fostering team engagement are crucial to successfully overseeing formulation projects from early development to scale-up.
What are the key skills and qualifications needed to thrive as a Telecommute Director Formulation Development, and why are they important?
To thrive as a Telecommute Director Formulation Development, you need an advanced degree in pharmaceutical sciences or chemistry, extensive experience in drug formulation, and leadership in R&D. Proficiency with formulation software, regulatory submission platforms, and familiarity with GMP/GLP guidelines or certifications are typically required. Exceptional project management, communication, and cross-functional collaboration skills help drive virtual teams and align stakeholders. These competencies ensure effective formulation development, regulatory compliance, and successful product launches in a remote environment.
What is the difference between Telecommute Director Formulation Development vs Telecommute Formulation Scientist?
| Aspect | Telecommute Director Formulation Development | Telecommute Formulation Scientist |
|---|---|---|
| Credentials | Advanced degree (PhD or MS), extensive industry experience | Bachelor's or Master's degree in Chemistry, Pharmacy, or related field |
| Work Environment | Leadership role overseeing teams and projects remotely | Hands-on research and formulation work, often collaborative but can be remote |
| Industry Usage | Used in pharmaceutical and biotech companies for strategic formulation leadership | Commonly employed in R&D labs for developing formulations |
The main difference is that the Telecommute Director Formulation Development focuses on leading formulation teams and strategic planning remotely, while the Telecommute Formulation Scientist is involved in hands-on formulation research and development. The director role requires more experience and leadership skills, whereas the scientist role emphasizes technical expertise in formulation science.
What does a Telecommute Director of Formulation Development do?
A Telecommute Director of Formulation Development oversees the design and improvement of pharmaceutical or chemical formulations while working remotely. This leadership role involves managing teams, coordinating cross-functional projects, ensuring regulatory compliance, and driving innovation in product development. They work closely with research, quality, and manufacturing departments to ensure products meet safety, efficacy, and quality standards, all while leveraging remote collaboration tools.
What are popular job titles related to Telecommute Director Formulation Development jobs in Florida? For Telecommute Director Formulation Development jobs in Florida, the most frequently searched job titles are:
What job categories do people searching Telecommute Director Formulation Development jobs in Florida look for? The top searched job categories for Telecommute Director Formulation Development jobs in Florida are:
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Full-time
Posted 3 days ago
Job description
Quotient Sciences: Molecule to Cure. Fast.
Quotient Sciences is a leading drug development and manufacturing accelerator, helping biotech and pharma companies bring new medicines to patients faster. With over 35 years of experience and a track record of success, we provide Drug Product (CDMO) and Clinical (CRO) services across the entire development pathway, including formulation development, clinical pharmacology, clinical trials, and commercial product manufacturing.
Our proprietary and disruptive platform - "Translational Pharmaceutics®" - integrates Drug Product Manufacturing and Clinical Testing to eliminate silos in the drug development process. This in turn reduces costs, improves outcomes, and significantly accelerates drug development times.
Why join us:
Because every day counts when bringing new medicines to patients. Our 1,000+ experts across the US, UK, and beyond are united by science, agility, and a culture that turns ideas into impact-fast.
An excellent opportunity for a Principal Investigator/ Medical Director to join Quotient Sciences - Miami, a dedicated, state-of-the-art, clinical pharmacology facility.
The Miami site specializes in phase I clinical pharmacology studies with a proven track record of almost a thousand studies over the past 25 years. With 144 beds and a large recruitment database of 20,000 healthy volunteers, we're known for being able to rapidly start up new studies in record time and complete studies quickly with full cohorts of subjects.
Join us as a Principal Investigator/ Medical Director and help us to develop new medicines and get them to patients faster.
The Role:
Main Tasks and Responsibilities:
Additional Tasks and Responsibilities:
The Candidate:
Job Demands:
Application Requirements
When applying for a position with Quotient Sciences to be able to work in our organization you must be aged 18 years or over and not have been debarred by the FDA. If you indicate you are under the age of 18 or have been debarred then your application will be automatically declined.
Our Commitment to Diversity, Equity and Inclusion
Quotient Sciences are advocates for positive change and conscious inclusion. We strive to create a diverse Quotient workforce and develop a workplace culture that provides a sense of acceptance for every person within our organization. As a global employer, we recognize the value in having an organization that is a true reflection and representation of our society today.
Specifically we will not discriminate on the basis of race, color, creed, religion, gender, gender identity, pregnancy, marital status, partnership status, domestic violence victim status, sexual orientation, age, national origin, alienage or citizenship status, veteran or military status, disability, medical condition, genetic information, caregiver status, unemployment status or any other characteristic prohibited by federal, state and/or local laws.
This applies to all aspects of employment, including hiring, promotion, demotion, compensation, training, working conditions, transfer, job assignments, benefits, layoff, and termination.
Quotient Sciences is a leading drug development and manufacturing accelerator, helping biotech and pharma companies bring new medicines to patients faster. With over 35 years of experience and a track record of success, we provide Drug Product (CDMO) and Clinical (CRO) services across the entire development pathway, including formulation development, clinical pharmacology, clinical trials, and commercial product manufacturing.
Our proprietary and disruptive platform - "Translational Pharmaceutics®" - integrates Drug Product Manufacturing and Clinical Testing to eliminate silos in the drug development process. This in turn reduces costs, improves outcomes, and significantly accelerates drug development times.
Why join us:
Because every day counts when bringing new medicines to patients. Our 1,000+ experts across the US, UK, and beyond are united by science, agility, and a culture that turns ideas into impact-fast.
An excellent opportunity for a Principal Investigator/ Medical Director to join Quotient Sciences - Miami, a dedicated, state-of-the-art, clinical pharmacology facility.
The Miami site specializes in phase I clinical pharmacology studies with a proven track record of almost a thousand studies over the past 25 years. With 144 beds and a large recruitment database of 20,000 healthy volunteers, we're known for being able to rapidly start up new studies in record time and complete studies quickly with full cohorts of subjects.
Join us as a Principal Investigator/ Medical Director and help us to develop new medicines and get them to patients faster.
The Role:
- Serve as Principal Investigator or Sub-Investigator on protocols undertaken by Quotient Sciences-Miami and is responsible for overseeing medical services and licensed professional staff
- Comply & adhere to GCP guidelines and regulations
- Ensure study data is collected in accordance with Good Clinical Practice (GCP) standards
- Ensure subject safety at all times
Main Tasks and Responsibilities:
- Serve as Principal Investigator or Sub-Investigator on FDA form 1572 for protocols conducted.
- Satisfactorily perform and comply with all responsibilities of a clinical investigator including, but not limited to those specified in the ICH Guidelines for Good Clinical Practice, FDA form1572, FDA Rules and Regulations and other Investigator's obligations specified in pharmaceutical company protocols and contracts
- Supervise morning drug administration at the overnight facility on those days when pharmacokinetic profiles are obtained or Physician presence is required for safety purposes
- Directly supervise the final selection of study participants from the time of clinic admission until actual drug exposure takes place
- Attends to adverse medical events
- Perform physical exams, read ECG's and review laboratory data for protocols conducted
- Review screening results as necessary to assemble qualified research participant cohorts according to protocol stipulations
- Work in concert with site and Clinical Operations to provide supervision and organization of physician, sub-Investigators, nurses and clinical staff
- Maintain familiarity with crash cart and emergency resuscitation procedures
- Participate in on-call rotation
- Review completed data entry and sign-off of completed study documentation in a timely manner including a careful review and sign-off of adverse assessments, study interim summaries, as well as clinical study reports
- Participate in writing and editing of protocols and informed consents for clinical studies
- Be available and participate in communications with sponsor in regard to study progress
- Be available for FDA inspections and Pharmaceutical Sponsor Audits
Additional Tasks and Responsibilities:
- Review SOPs and assist with SOP revisions when applicable
- Assist in drafting Notes to File
- Identify quality issues and help draft and implement CAPAs
- Attend department and sponsor meetings
- Assist in training new staff (other MDs and/or ARNPs/PAs) as necessary
- Give educational lectures and participates in Mock Code training as necessary
The Candidate:
- Active Medical Doctor or Doctor of Osteopathy License, State of Florida
- Minimum of five years of clinical research experience preferred
- Board Certified in a medical specialty
- Must not be debarred, disqualified, or restricted by the FDA or State of Florida
- Maintains BLS and ACLS certification
- Maintains CITI Program certification
Job Demands:
- The job may involve the following:
- Very high concentration of work
- Strict and tight deadlines
- Having to juggle a range of tasks/issues simultaneously
- Working in a hazardous environment with high requirement to follow safety procedures
- Working outside normal working hours
- Needing to respond to client demands
Application Requirements
When applying for a position with Quotient Sciences to be able to work in our organization you must be aged 18 years or over and not have been debarred by the FDA. If you indicate you are under the age of 18 or have been debarred then your application will be automatically declined.
Our Commitment to Diversity, Equity and Inclusion
Quotient Sciences are advocates for positive change and conscious inclusion. We strive to create a diverse Quotient workforce and develop a workplace culture that provides a sense of acceptance for every person within our organization. As a global employer, we recognize the value in having an organization that is a true reflection and representation of our society today.
Specifically we will not discriminate on the basis of race, color, creed, religion, gender, gender identity, pregnancy, marital status, partnership status, domestic violence victim status, sexual orientation, age, national origin, alienage or citizenship status, veteran or military status, disability, medical condition, genetic information, caregiver status, unemployment status or any other characteristic prohibited by federal, state and/or local laws.
This applies to all aspects of employment, including hiring, promotion, demotion, compensation, training, working conditions, transfer, job assignments, benefits, layoff, and termination.