Skip to content
CV Rocket
Get started
How it worksThe enginePricingBlogContactSign in

Open nowPosted 4 days ago

Clinical Pharmacology Consultant

Entrada Therapeutics8 open roles

Where
US
Work mode
Remote
Get the CV for this job

From $25 per CV, paid once. No subscription.

Your applicationOpen nowClinical Pharmacology ConsultantEntrada Therapeutics · US

  1. YouYes, apply to this one.

  2. CV RocketCV written for this posting.

  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

  4. CV RocketApplied on Entrada Therapeutics's own form.

The reply lands in your private mailbox

3×more interviews than doing it yourself with ChatGPT.

The clock on this job

Early applications get read.

12.3% of postings close within 7 days. Measured by our own scanner across the market. Entrada Therapeutics postings stay open a median of 26 days.

Share of postings closed within
  1. 2.1%1 day
  2. 4.5%3 days
  3. 12.3%7 days
  4. 19.3%14 days
  5. 35.6%30 days
  6. 58.1%60 days
This job: posted 4 days ago

Entrada Therapeutics median: 26 days open

The posting

This position is listed on behalf of a partner company, which manages all applications and next steps. Our partner is looking for a Clinical Pharmacology Consultant based in the United States.

We are seeking an experienced Clinical Pharmacology Consultant to support the development of innovative therapies for patients with rare and inherited diseases. In this remote contract role, you will bring specialized expertise in clinical pharmacology to clinical-stage drug development programs, helping translate complex scientific data into meaningful insights that inform clinical and regulatory decisions. You will play a key role in study design, pharmacokinetic and pharmacodynamic data analysis, and the preparation of clinical and regulatory documentation. Working closely with multidisciplinary teams, you will contribute to advancing development programs from early clinical exploration through later-stage studies. This opportunity is ideal for a scientifically rigorous professional who enjoys solving complex problems, collaborating across functions, and making a tangible contribution to the development of potentially life-changing medicines.

Accountabilities

  • Provide clinical pharmacology expertise and input for regulatory submissions and other development documentation.
  • Contribute to clinical study design and the preparation and review of study documents, including laboratory manuals, clinical protocols, and statistical analysis plans (SAPs).
  • Independently lead and oversee the analysis, interpretation, integration, and reporting of clinical pharmacokinetic (PK) and pharmacodynamic (PD) data for assigned projects.
  • Collaborate with cross-functional stakeholders across Clinical Development, Biostatistics, Non-Clinical Product Development, Clinical Operations, and Regulatory Affairs to support project milestones and broader organizational objectives.
  • Oversee work performed by contract research organizations (CROs) and external vendors, ensuring alignment with approved protocols, quality standards, and project timelines.
  • Apply scientific judgment and analytical expertise to help guide clinical development decisions and strengthen the evidence supporting investigational therapies.
  • Master’s degree with at least 8 years of relevant experience, Ph.D. with at least 3 years of relevant experience, or Pharm.D. or M.D. with applicable experience in pharmaceutical sciences, pharmacology, pharmacometrics, pharmacokinetics, or a related discipline.
  • Demonstrated experience in clinical pharmacology and clinical study design within the biotechnology or pharmaceutical industry.
  • Strong understanding of clinical PK/PD data analysis, interpretation, integration, and reporting.
  • Experience with pharmacokinetic analysis and modeling software, such as Phoenix WinNonlin, R, NONMEM, MATLAB, or comparable tools.
  • Strong mathematical modeling, quantitative analysis, problem-solving, and scientific communication skills.
  • Experience spanning early exploratory clinical trials through Phase 2 or Phase 3 programs is preferred, along with a relevant publication record.
  • Experience with compartmental PK/PD modeling is an advantage.
  • Ability to work independently, manage assigned project responsibilities, and collaborate effectively with multidisciplinary teams and external partners.
  • A curious, creative, and persistent approach to scientific challenges, with a strong commitment to collaboration and patient-focused drug development.
  • Remote flexibility: Work remotely from within the United States.
  • Contract engagement: A flexible consulting opportunity offering approximately 30–40 hours per week.
  • Scientific impact: Contribute to clinical-stage development programs targeting rare and inherited diseases.
  • Cross-functional collaboration: Partner with experts across clinical development, biostatistics, non-clinical development, clinical operations, and regulatory functions.
  • Professional contribution: Apply advanced clinical pharmacology and quantitative modeling expertise to support evidence-based development decisions.
  • Compensation and additional benefits: Salary or hourly rate, healthcare coverage, paid time off, and other benefits were not specified in the original posting.

How Jobgether works:

We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team.

We appreciate your interest and wish you the best!

Why Apply Through Jobgether?

Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time.

#LI-CL1

From $25, paid onceGet the CV for this job

What happens when you press

One press. We do the rest.

  1. A CV for this posting

    Written against Entrada Therapeutics's own wording, from every piece of relevant proof in your profile.

  2. 25 readers review it

    Recruiter, hiring manager, skeptic and more read every draft, round after round. You get the best round.

    The review screen in CV Rocket: how each CV was read, round by round.

  3. We apply on Entrada Therapeutics's form

    Our application engine gets through the hardest forms there are. Where a question needs you, AI suggests the best answer. Don't want us applying from our IP addresses? Use our Chrome extension: we apply straight from your own browser.

    An application in CV Rocket: every answer filled in on the employer's form.

  4. Every reply, sorted

    Entrada Therapeutics's answer lands in your private mailbox, and we classify it on arrival: interview, question, rejection.

    The CV Rocket inbox: each employer reply classified as an interview, an action or a rejection.

  5. Reply with AI

    AI helps you write the email, checks it and sends it. We show you whether the recruiter read it.

  6. The interview in your calendar

    Full integration with your calendar. The invitation goes straight in.

    An interview invitation in the CV Rocket inbox, added to the candidate's calendar.
Get the CV for this job

From $25 per CV, paid once. No subscription.

Why it works

3×

more interviews than doing it yourself with ChatGPT.

ChatGPT writes a CV and never learns what happened to it. We see every reply. For each CV we know:

  • How it was written, and how the review scored it
  • When we applied, and how long after the posting went up
  • Which posting, which company, which city
  • Who got the interview, and who heard nothing

That is how we know which CVs get called.

Get the CV for this job

From $25 per CV, paid once. No subscription.

The numbers game

More applications. More interviews.

Every application goes out with its own CV, written for that posting and paid once. Send enough of them and the law of large numbers finds you the job.

Get the CV for this job
By hand5–10
With CV Rocket100
applications a day

Nearby

Live postings like this one

Same employer first, then the same role elsewhere.

Before you press

Straight answers

Get the CV for this job

From $25 per CV, paid once. No subscription.

What if my background isn't good enough?

We make the most of the background you have. The CV uses every piece of relevant proof your profile holds, and one of the 25 readers reads your whole profile and flags what the CV left out.

Do you really apply for me?

Yes, on the employer's own form, the hardest ones included. Where a question needs you, you answer it right there and AI suggests the best answer. Don't want us applying from our IP addresses? Use our Chrome extension: we apply straight from your own browser.

Is it a subscription?

No. You pay once per CV, from $25. Every application goes out with its own CV, written for that posting.

One job. One CV.
Paid once.

Pick the posting you want. We write for it, apply for you and catch the reply.

Get the CV for this job

From $25 per CV, paid once. No subscription.