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

Open nowPosted 8 hours ago

PV Regulatory Intelligence & Partner Alliance Manager (12 months FTC)

Clinigen

Where
Burton upon Trent, England, United Kingdom
Get the CV for this job

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

Your applicationOpen nowPV Regulatory Intelligence & Partner Alliance Manager (12 months FTC)Clinigen · Burton upon Trent, England, United Kingdom

  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 Clinigen'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.

13.7% of postings close within 7 days. Measured by our own scanner across the market.

Share of postings closed within
  1. 2.3%1 day
  2. 4.8%3 days
  3. 13.7%7 days
  4. 22.1%14 days
  5. 37.6%30 days
  6. 59.1%60 days
This job: posted 8 hours ago

The posting

The Pharmacovigilance Regulatory Intelligence & Partner Alliance Manager is responsible for overseeing the lifecycle of pharmacovigilance agreements and partnerships, ensuring compliance with global pharmacovigilance requirements and supporting the safe and effective management of medicinal products across international markets.

The role acts as a subject matter expert in pharmacovigilance regulatory intelligence, monitoring evolving regulatory requirements and ensuring that company processes, procedures and partner agreements remain compliant with applicable legislation and client expectations. Working collaboratively with internal stakeholders, clients and external partners, the role plays a key part in maintaining an effective global pharmacovigilance framework and supporting Clinigen's commitment to patient safety.

Key Responsibilities

  • Lead the development, negotiation, implementation and maintenance of pharmacovigilance agreements and partnerships.
  • Serve as the subject matter expert for global pharmacovigilance regulatory requirements and regulatory intelligence activities.
  • Monitor and assess evolving pharmacovigilance legislation and guidance, identifying impacts to business processes and compliance obligations.
  • Coordinate cross-functional implementation of regulatory changes and monitor ongoing compliance.
  • Develop and maintain a global network of pharmacovigilance partners and consultants to support local pharmacovigilance activities.
  • Provide oversight of partner compliance, including participation in audits, governance meetings and corrective action management.
  • Support clients and internal stakeholders with expert advice on pharmacovigilance requirements, including early access and unlicensed medicine programmes.
  • Build and maintain effective relationships with clients, alliance partners, industry associations and regulatory authorities.

Requirements

Essential

  • Bachelor's degree in Life Sciences, Pharmacy, Medicine or a related scientific discipline.
  • Significant experience within pharmacovigilance, including knowledge of global pharmacovigilance regulations and requirements.
  • Experience negotiating and managing pharmacovigilance agreements and external partnerships.
  • Strong understanding of pharmacovigilance legislation and regulatory compliance requirements.
  • Experience conducting regulatory impact assessments and implementing regulatory changes.
  • Excellent project management, organisational and stakeholder management skills.
  • Strong communication, negotiation and influencing abilities.
  • Ability to work effectively across global, cross-functional teams.
  • Proficiency with Microsoft Office applications and relevant pharmacovigilance systems.

Desirable

  • Experience within early access, compassionate use or unlicensed medicines programmes.
  • Experience working within a commercial pharmaceutical environment.
  • Experience supporting alliance management, partner governance or international vendor management activities.
  • Knowledge of pharmacovigilance regulatory intelligence processes and tools.
  • Experience working in a global or multicultural environment.

What We're Looking For

  • A proactive and solutions-focused approach.
  • Strong attention to detail and commitment to quality and compliance.
  • Ability to manage multiple priorities in a fast-paced and evolving environment.
  • A collaborative team player with the confidence to influence and engage stakeholders at all levels.
  • Passion for patient safety and maintaining high standards of pharmacovigilance compliance.
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 Clinigen'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 Clinigen'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

    Clinigen'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

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.