Top 39 Clinical toxicology Jobs in Remote

Non-Clinical Regulatory Consultant
Pintail Solutions —Remote
- Part-time
- 5 years
- Bachelor's degree
- Travel
Quick Apply
2d
Senior Scientist / Engineer: Immunology, Nucleic Acid Therapeutics, Synthetic Biology, & Cell Engineering
Intertwine Associates —Remote
- $90,000 - $220,000 a year
- Full-time
- Doctor of Philosophy
- Budgeting
- Senior level
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Director, Toxicology
Certara —Remote
- Full-time
- Microsoft Word
- Writing skills
- Doctor of Philosophy
3d
Homeopathic Per Diem Consultants
Lachman Consultant Services —Remote
- Online Application
- Bachelor of Science
- Bachelor's degree
- Manufacturing
Research Fellow, Pharma Toxicology
Bausch + Lomb —Remote
- $150,000 - $200,000 a year
- 11+ years
- Doctor of Philosophy
- Team management
- Paid time off
- Retirement plan
Senior Scientist - Translational Safety & Risk Sciences (TSRS)
Amgen —San Francisco, CA
- $129,228.90 - $174,839.10 a year
- Remote
- Medicine
- 3 years
- Bachelor's degree
- Disability insurance
- Health insurance
Principal Medical Writer
AbbVie —Chicago, IL
- $109,500 - $208,500 a year
- Full-time
- Remote
- Word processing
- English
- Windows
- Paid holidays
- Health insurance
8d
Account Coordinator (Remote)
Clinical Reference Laboratory —Lenexa, KS
- $18 - $31 an hour
- Overtime
- Remote
- Microsoft Excel
- Microsoft Outlook
- Writing skills
- AD&D insurance
- Paid holidays
Clinical Trial Management Associate
Ionis Pharmaceuticals, Inc. —Carlsbad, CA
- $88,776 - $133,156 a year
- Remote
- HIPAA
- Mid-level
- Bachelor's degree
Quick Apply
2d
Research Fellow, Medical Device Toxicologist
Bausch + Lomb —Remote
- $150,000 - $200,000 a year
- 11+ years
- Doctor of Philosophy
- Mentoring
- Paid time off
- Retirement plan
Director, Business Development – Toxicology Lab Services
QPS, LLC —Newark, DE
- $120,000 - $150,000 a year
- Full-time
- Remote
- Master's degree
- Bachelor's degree
- Senior level
Quick Apply
Director, Nonclinical Safety, Pathology
Gilead Sciences —Foster City, CA
- $205,615 - $292,710 a year
- Full-time
- Remote
- 3 years
- Analysis skills
- Presentation skills
- Health insurance
- Dental insurance
Medical Director / Senior Medical Director
Neumora —Chicago, IL
- $289,800 - $367,934 a year
- Remote
- Medicine
- Psychiatry
- 3 years
- Employee stock purchase plan
- Disability insurance
Quick Apply
9d
Executive Medical Director, Neurology, Clinical Development (Remote)
Penfield Search Partners —Fairfield, CT
- Contract
- Remote
- Medicine
- 5 years
- Doctor of Philosophy
Quick Apply
8d
Medical Toxicologist TDH Poison Center (Per Diem < 20 hours/week)
UTMB Health —Remote
- Part-time
- Remote
- Medicine
- BC/BE
- US work authorization
Senior Director Nonclinical Development
Viatris —Remote
- $151,000 - $314,000 a year
- Full-time
- Remote
- 11+ years
- English
- Ability to climb stairs
Head of Strategic Alliances
Merative —Remote
- $255,569.37 - $383,354.05 a year
- Full-time
- Senior level
- Commercial
- Health insurance
- Dental insurance
Senior FIFRA Regulatory Affairs Manager (part-time) (f/m/d)
knoell —Remote
- Part-time
- Remote
- Data analysis skills
- 8 years
- Bachelor's degree
- Work from home
- Referral program
Quick Apply
Executive Director, Clinical Development - Neurology
Insmed Incorporated —Bridgewater, NJ
- $306,000 - $417,000 a year
- Full-time
- Remote
- Medicine
- 5 years
- Doctor of Philosophy
- Employee stock purchase plan
- Disability insurance
Preclinical V&V Specialist
KLS MARTIN LP —Jacksonville, FL
- Full-time
- Remote
- Bachelor of Science
- Office
- Presentation skills
- Paid parental leave
- Parental leave
1d

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clinical toxicology jobs near remote

Non-Clinical Regulatory Consultant

Pintail Solutions
Remote

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Job Details

Part-time
2 days ago

Qualifications

FDA submissions
Investigational new drug (IND) applications
Bachelor's degree
Toxicology
Video conferences (communication methods)
Pharmacokinetics

Full Job Description

Job Description

Job Title

Non-Clinical Regulatory Consultant

Position Type

Part Time Contractor

Location

Remote

Travel Required

N/A

External Posting URL

Applications Accepted By

Jason C. Bork
[email protected]
Or (317) 694-0232 (mobile)

Mail:
Jason C. Bork
Pintail Solutions
12175 Visionary Way, Suite 1040
Fishers, IN 46038

Job Description

Overview
Pintail Solutions is a trusted life science partner improving global health. We work with a variety of clients including nonprofits, biotechs and pharmaceutical companies, and academic institutions. Clients work with Pintail because of our breadth of experience, our ability to deliver outcomes, and our passion for every project we work on. We focus on the greater good of the client and are fearless about informing clients about what they need instead of what they may ask for. We expect everyone in the company to act like an owner and be insatiable about looking for ways to improve. We value excellence, integrity, and collaboration, and we believe we will make a greater difference in our work when we are having fun doing it.

A client is looking for a regulatory consult on the FDA pre-IND feedback they received ~2 yrs ago, the CRO's large animal dermal toxicology and pharmacokinetic study plans, and scientific and regulatory evaluation of the potential toxicity of the lotion excipients.

We are seeking experienced Regulatory Consultants, with dermal TK/PK experience in minipigs. This engagement is expected to start ASAP and last 1-2 months (est. 30-50 hrs of work). The review is expected to include:

Whether the proposed studies adequately address the FDA feedback;
Whether the study designs, dose levels, durations, recovery groups, animal numbers, endpoints, and application sites are appropriate;
Whether any proposed studies or endpoints appear duplicative, unnecessary, or insufficient;
Whether the irritation, sensitization, systemic exposure, and local-tissue pharmacokinetic strategies are appropriate;
Whether the excipient package raises any additional nonclinical safety concerns;
Identification of important gaps or recommended modifications; and
An overall assessment of whether the proposed package is sufficient to support the planned initial clinical study.

This individual will need to be motivated, driven, and have FDA IND-enabling experience. A a mature business presence to successfully engage with internal and external business partners is required.

The following roles and responsibilities entail most of what this role may be asked to do but will expand based on the individual’s and organization’s needs.

Roles and Responsibilities
Document Review

Review documents noted above for the purpose of answering documented questions
Complete independent research and assessment to answer the questions included above

Communication, Assessment and Write-up

Develop written summary and gap analysis with prioritized recommendations
Share perspectives and findings via video meeting
Revise written document as necessary

Qualifications and Education Requirements
Candidates should have a 4-year college degree, at least 5 yrs regulatory experience including pre-IND enabling non-clinical work, dermal TK/PD studies, and experience with testing in minipigs. Candidates should have strong writing skills and always maintain a professional presence.

Preferred Skills
Candidates need to thrive in a dynamic, service-minded, entrepreneurial environment. Business maturity and effective communication skills are required as the role will engage with key partners and executives. Candidates should desire to be part of a collaborative team of professionals and be interested in continually learning and developing. They should enjoy working with people, organizing information, supporting client success, and helping teams stay aligned. They should be comfortable operating in a healthcare technology environment where accuracy, professionalism, and clear communication matter.

Additional Notes
Travel is not expected.

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Refine Your Search

clinical toxicology jobs in remote

Non-Clinical Regulatory Consultant

Senior Scientist / Engineer: Immunology, Nucleic Acid Therapeutics, Synthetic Biology, & Cell Engineering

Director, Toxicology

Homeopathic Per Diem Consultants

Research Fellow, Pharma Toxicology

Senior Scientist - Translational Safety & Risk Sciences (TSRS)

Principal Medical Writer

Account Coordinator (Remote)

Clinical Trial Management Associate

Research Fellow, Medical Device Toxicologist

Director, Business Development – Toxicology Lab Services

Director, Nonclinical Safety, Pathology

Medical Director / Senior Medical Director

Executive Medical Director, Neurology, Clinical Development (Remote)

Medical Toxicologist TDH Poison Center (Per Diem < 20 hours/week)

Senior Director Nonclinical Development

Head of Strategic Alliances

Senior FIFRA Regulatory Affairs Manager (part-time) (f/m/d)

Executive Director, Clinical Development - Neurology

Preclinical V&V Specialist

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