Medical Toxicologist

ALKU; United States; Remote; USD 70,000 - 120,000; Full time

Job summary

ALKU is seeking a Clinical Trial Proposal Consultant with expertise in medical toxicology to assist with a crucial clinical trial proposal. The candidate will be responsible for budget development and creating responses for a pharmaceutical sponsor. Remote work is available for this 6-month contract position, making it an ideal opportunity for professionals with a background in CROs and trial management.

Qualifications

• Experience in CRO and medical toxicology required.
• Experience with budget development for clinical trials.
• Experience with informed consent or community consent trials.

Responsibilities

• Developing budgets and formulating responses to sponsors.
• Creating protocols for emergency treatment trials.
• Supporting the clinical trial proposal phase.

Skills

Experience working in a CRO

Medical toxicology experience

Experience with budget development

Experience with informed consent patient trials

Community consent trials experience

Job description

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Clinical Trial Proposal Consultant - Medical Toxicology

6 months + remote

Project:

Our client is a large research group. They were approached by a pharmaceutical sponsor to conduct a clinical trial for them and put together a budget. This is a study that will be done for emergency basis treatments done by ER or EMS professionals in the field. All participants in the trials are either informed consent patients, or community consent. A candidate with experience in these types of trials is preferred. The most important need is within budget development and support formulating a response to the sponsor company for this specific clinical trial, technical protocol development, and medical toxicology experience is a must. No therapeutic area preference. This study will be done by EMS units out in the field, so the ask is to take the protocol and spreadsheet of information provided by the pharmaceutical sponsor and create the budget for this trial from a CRO perspective. This is in the proposal development phase, so this person is needed to help formulate the response to the pharmaceutical sponsor and potentially stay on if the client is awarded awarded the study.

Required Skills:

-Experience working in a CRO

-Medical toxicology experience

-Experience with budget development for trials and formulating responses to sponsor companies from a CRO perspective

-Experience with informed consent patient trials OR community consent trials

Seniority level

• Seniority level

  Not Applicable

Employment type

• Employment type

  Contract

Job function

• Job function

  Consulting and Science

• Industries

  Pharmaceutical Manufacturing and Biotechnology Research

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