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

Open nowPosted 65 days ago

Regional Scientific Director, Mid-Atlantic

intelliatx15 open roles

Pay
$216,000 – $264,000 a year
Where
Cambridge, MA
Get the CV for this job

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

Your applicationOpen nowRegional Scientific Director, Mid-Atlanticintelliatx · Cambridge, MA

  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 intelliatx'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.

9.8% of postings close within 7 days. Measured by our own scanner across the market. intelliatx postings stay open a median of 9 days.

Share of postings closed within
  1. 1.9%1 day
  2. 3.9%3 days
  3. 9.8%7 days
  4. 15.5%14 days
  5. 33.7%30 days
This job: posted 65 days ago

intelliatx median: 9 days open

The posting

Why Join Intellia?

Our mission is to develop curative genome editing treatments that can positively transform the lives of people living with severe and life-threatening diseases.

Beyond our science, we live our four core values: One, Explore, Disrupt, Deliver and feel strongly that you can achieve more at Intellia. We have a single-minded determination to excel and succeed together. We believe in the power of curiosity and pushing boundaries. We welcome challenging thoughts and imagination to develop innovative solutions. And we know that patients are counting on us to make the promise a reality, so we must maintain high standards and get it done.

We want all of our people to go beyond what is possible. We aren’t constrained by typical end rails, and we aren’t out to just “treat” people. We’re all in this for something more. We’re driven to cure and motivated for change. Just imagine the possibilities of what we can do together.

How You Will Achieve More:

The Regional Scientific Director (Associate Director level) serves in a customer-facing medical role to establish trusted partnerships within the healthcare community covering Intellia’s CRISPR-based, first-in-class gene editing programs. Key responsibilities include scientific exchange, medical education and insight identification with PIs, KOLs, healthcare multidisciplinary teams and referral HCPs. RSDs will support both the nex-z and lonvo-z programs.

Mid-Atlantic Region will include: Maryland, Washington, D.C., Delaware, Virginia, West Virginia, North Carolina, South Carolina

Responsibilities:

The RSDs will focus their engagement efforts to KOLs and trial sites providing the following:

Scientific Engagement Activities

  • Engagement with KOLs across ATTR amyloidosis and HAE within territory to provide education on our CRISPR gene editing platform and reactively educate on the MoA and clinical data on nex-z and lonvo-z.
  • Understanding of patient journey at key centers and identification of site capabilities and preferences regarding gene editing.
  • Development of individualized scientific engagement plans for key KOLs aligned with scientific narrative and medical strategy.
  • Identify external insights and knowledge gaps through listening for key intelligence topics of interest and timely reporting via CRM
  • Medical Congress attendance to enable KOL engagement, medical booth staffing, scientific session coverage, insights gathering and reporting
  • Institutional presentations on Intellia scientific evidence, as appropriate.

Clinical Trial Awareness and Enrollment Focused Activities

  • Provide scientific support for Phase 3 clinical trials during site start up, activation and recruitment through scientific education and operational insights
  • Establish, cultivate, and maintain scientific relationships with Investigators and study site teams
  • Identify barriers to site activation and/or patient recruitment, and discuss solutions with Investigators, study site teams, and institutional administrative team members to address and remove these barriers.
  • Escalate site feedback or concerns to Intellia clinical teams
  • Develop a robust understanding of clinical practice and referral associated with gene editing therapies.
  • Ensure compliance and high level of scientific integrity in all interactions, including completion of trainings on time and adherence to policies

About You:

  • Demonstrated success working in a highly matrixed, cross-functional environment.
  • Ability to critically assess situations to prioritize the importance, urgency and risks, and present leadership with recommendations.
  • Ability to anticipate change and to flexibly adapt to changing business needs.
  • Self-starter and team player with a collaborative spirit and results orientation.
  • Organized, able to multi-task to meet timelines in a fast-paced environment with strong attention to accuracy and detail.
  • Excellent presentation, communication, and project management skills across a variety of interaction mediums including in person, digital, email, phone, etc.
  • Ability to understand and clearly and effectively communicate complex scientific and medical information to both internal and external stakeholders.
  • Excellent written and oral communication skills are imperative; strong interpersonal skills commensurate with the need to collaborate closely with partners, investigators, contractors, consultants, and team members across functions.
  • Established track record of effective and influential oral presentations to both large and small audiences within the healthcare profession.
  • Ability to complete required training, documentation, expense reporting, and other administrative tasks.
  • Willingness and ability to travel 50-70% including overnight stays.
  • Ability to manage a geographically assigned territory from a home-based office.
  • Computer skills including Excel, Word, Power Point, Outlook, and programs such as Zoom are expected.
  • Valid driver’s license
  • Doctorate level or terminal degree (Pharm.D., Ph.D., M.D. or D.O.)
  • 3+ years industry or related field experience.
  • Extensive clinical trial experience including Phase 3 trials
  • Prior pharmaceutical industry experience as a MSL/RSD with solid understanding of scientific exchange in the context of compliance/ regulated environment and robust experience supporting execution of clinical trial.
  • Therapeutic knowledge in allergy/immunology/HAE, cardiology/ATTR-CM/-PN, or genetic medicine highly preferred.
  • New product launch experience highly preferred.
  • Ability to sit or stand for multiple hours at a computer
  • Manual dexterity for keyboarding; may include repetitive movements

#LI-Remote

EEOC Statement: Intellia believes in a diverse environment, and is committed to equal employment opportunity for all its employees and qualified applicants. We do not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Intellia will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

Applications are accepted on a rolling basis, and will continue to be accepted until the position is filled at which point the position will be taken down.

The base salary for this position is expected to range between $216,000.00 - $264,000.00 USD per year.

The salary offered is determined based on a range of factors including, but not limited to, relevant education and training, overall related experience, specialized, rare or in-demand skill sets, internal comparators and other business needs. Upon joining Intellia, your salary will be reviewed periodically and additional factors such as time in role and performance will be considered. Intellia may change the published salary range based on company and market factors.

Additional compensation includes a performance-based annual cash bonus, a new hire equity grant, and eligibility to be considered for annual equity awards the value of which are determined annually at the Company’s discretion.

For more information about Intellia’s benefits, please click here.

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 intelliatx'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 intelliatx'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

    intelliatx'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.