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

Open nowPosted 5 days ago

PRN Investigational Drug (IND) Specialist

The US Oncology Network849 open roles

Where
Nashville, Tennessee, United States
Get the CV for this job

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

Your applicationOpen nowPRN Investigational Drug (IND) SpecialistThe US Oncology Network · Nashville, Tennessee, United States

  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 The US Oncology Network'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. The US Oncology Network postings stay open a median of 1 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 5 days ago

The US Oncology Network median: 1 days open

The posting

Overview

SCRI Oncology Partners, located in Nashville, Tenn., is a dedicated cancer treatment practice led by globally recognized oncologists with disease expertise in cancer care and clinical research. This practice offers patients state-of-the art personalized cancer care and opportunities to participate in clinical trials with innovative treatments. The practice conducts clinical trials through their affiliation with Sarah Cannon Research Institute (SCRI), a global leader in oncology research that has been offering and managing clinical trials in the community for over 30 years. Since its inception, SCRI-OP has contributed to pivotal research that has helped advance the majority of new cancer therapies approved by the FDA today.

Scope

Under minimal supervision, provides consultative support and training related to Investigational Drug (IND) for the SCRI Oncology Partners pharmacy program. Serves as a subject matter expert for investigational product accountability, disposition, reconciliation, and regulatory compliance following study completion. Collaborates with pharmacy staff, research personnel, sponsors, and investigators to ensure proper handling and documentation of investigational medications in accordance with Good Clinical Practice (GCP), FDA regulations, sponsor requirements, and organizational policies. Supports ongoing pharmacy staff education and competency development related to investigational drug processes.

Responsibilities

Key Responsibilities

  • Provides expertise regarding investigational drug (IND) accountability, inventory reconciliation, disposition, and destruction processes upon study closure.
  • Reviews and reconciles investigational drug records, accountability logs, temperature monitoring documentation, and sponsor-required closeout documentation.
  • Assists pharmacy leadership and research staff in identifying and resolving discrepancies related to investigational product inventory and documentation.
  • Coordinates and supports sponsor, monitor, and audit-related investigational drug closeout activities.
  • Ensures investigational products are managed and documented in accordance with protocol requirements, sponsor instructions, FDA regulations, GCP guidelines, and organizational policies.
  • Develops and delivers training programs for pharmacists, and pharmacy technicians on investigational drug management and closeout procedures.
  • Creates educational materials, standard work documents, job aids, and competency assessments related to investigational drug processes.
  • Evaluates existing workflows and recommends process improvements to enhance compliance, efficiency, and operational readiness.
  • Assists with preparation for internal audits and regulatory inspections involving investigational drug management.
  • Serves as a resource for pharmacy staff regarding investigational drug regulations, sponsor expectations, and best practices.
  • Collaborates with pharmacy leadership on quality assurance initiatives related to investigational drug services.
  • Maintains current knowledge of applicable FDA regulations, USP standards, GCP requirements, and investigational drug management practices.

Qualifications

Minimum Job Qualifications (Knowledge, Skills, & Abilities)

Education/Training

  • Minimum of High School Diploma in combination with required experience

Business Experience

  • Minimum 5 years of experience in oncology pharmacy, investigational drug services, research pharmacy, or clinical trial operations required.

Specialized Knowledge/Skills

  • Extensive knowledge of FDA regulations governing investigational drug management.
  • Strong understanding of GCP guidelines, sponsor requirements, and research compliance standards.
  • Experience with investigational drug accountability systems and documentation requirements.
  • Knowledge of oncology clinical trials and investigational oncology agents preferred.
  • Excellent communication, presentation, and training skills.
  • Strong organizational and project management abilities.
  • High attention to detail and accuracy.
  • Ability to function independently while collaborating effectively with multidisciplinary teams.
  • Proficient in Microsoft Office applications and electronic research systems.

Working Conditions

Environment

  • Traditional outpatient oncology clinic, pharmacy, and office environment.
  • May require occasional on-site support during audits, monitor visits, or staff training sessions.
  • Exposure to conditions common to an oncology practice and research environment.

Physical Requirements

  • Extended periods of computer-based work.
  • Ability to review and organize investigational drug records and documentation.
  • Occasional standing, walking, and lifting of study-related materials weighing up to 25 pounds.

Employment Status

PRN (As Needed)

This position is intended to provide intermittent expertise and operational support for investigational drug study closeout activities, pharmacy compliance reviews, staff education, competency validation, and process improvement initiatives. Hours will vary based on organizational needs, study volume, audit preparation activities, and training requirements.

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 The US Oncology Network'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 The US Oncology Network'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

    The US Oncology Network'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.