Cambridge, MA, USA
Posted: Feb 04, 2025
RemoteFull-time
Find Similar Recent Jobs
Share Job
Job Description
The Company

With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer. Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building.

The Role

Reporting to the Senior Director of Pharmacovigilance (PV) Operations, the Associate Director of PV Operations will be responsible for PV’s role in expanded & early access programs (EAP) across the portfolio and other PV-related projects as assigned (e.g., Cross-reporting of SUSAR; Support Call Center for PV-related questions). The role will expand and evolve in line with Nuvalent’s expansion as we approach potential market authorization.

Responsibilities

  • Oversight of EAP vendor, including, but not limited to, safety data exchange agreement maintenance and compliance monitoring
  • Adverse event reconciliation between databases
  • Oversight of safety reporting requirements for all EAP countries
  • Primary point of contact for PV requests within the EAPs
  • Support PV Operations team activities to ensure cross coverage across the portfolio
  • Support regulatory inspections and serve as subject matter expert on PV’s role in EAPs
  • Identify potential risks and opportunities within the EAPs, keeping PV Leadership informed for proactive decision-making

Competencies Include

  • Excellent oral and written communication skills with high emotional intelligence
  • Track record of effective decision-making and conflict management/resolution skills
  • Ability to work in a collaborative environment and build effective working relationships across the organization, and with external stakeholders/vendors
  • Detail and process orientated, with excellent project management, problem solving, and organization skills.
  • Ability to think critically with strong attention to detail, effectively communicating verbally and in writing.
  • Demonstrated project management and prioritization capabilities

Qualifications

  • Bachelor’s degree in a relevant field or related experience.
  • 8+ years of relevant experience within the biotechnology or pharmaceutical industry, including, 4+ years of experience in Pharmacovigilance operations
  • Hands-on expert knowledge of Argus or equivalent PV database.
  • Ability to interpret and follow regulatory guidelines.
  • Proven knowledge of Good Documentation Practices and cGXPs.
  • Basic knowledge of MedDRA coding.
  • Experience in ICSR case-processing and reporting.
  • Strong knowledge of current and emerging regulatory requirements including EMA GVP Modules, FDA IND and NDA reporting requirements, ICH, CIOMS
  • Expert knowledge of pharmacovigilance activities and processes, preferably in multiple PV functional areas
  • Direct experience managing relationships with service providers or external business partners

Nuvalent provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law.

Nuvalent is aware that many companies are dealing with fraudulent job postings on third-party employment search sites and/or individual(s) or entities claiming to be employees of such companies. Those involved are offering fraudulent employment opportunities to applicants, often asking for sensitive personal and financial information, and using such information for criminal activities.

Please be advised that all legitimate correspondence from a Nuvalent employee will come from "@nuvalent.com" email accounts. Automated system response emails from our Greenhouse applicant tracking system come from a “” email address. There are no variations of these email addresses and Nuvalent would not request personal and/or financial information via email. Job opportunities would only be extended after a completed job application is submitted by a candidate and a thorough interview process including 1:1 and/or group interviews via phone, video conferencing and/or in-person.

If you believe you have been contacted by anyone misrepresenting themselves as an employee of Nuvalent, please contact Nuvalent at 857-357-7000. Thank you.
Share Job
Additional Info
Min. Experience
-
Job Location Type
Remote
Job Type
Full-time
Predicted Seniority Level
Mid-Senior level
Job Duration
-
Language(s)
All
Est. Budget/Pay Rate
To be discussed
Est. hrs
-
Optimal Job Start
-
Job Industry
Biotechnology Research
Job Function
Research, Analyst, and Information Technology
Employer
Nuvalent, Inc.
Preferred Applicant Countries
United States
Job Ref
J25EE3248F23B
Disclaimer: The jobs on Lifelancer Platform are posted by employers, recruiters and Lifelancer. We aim to provide value to Talent users by connecting them with a maximum number of curated job opportunities. However, Lifelancer doesn't represent job-offering companies and is not responsible for job advert content or updates. We aim to connect you with the employer, job source, or application link to the best of our ability. You can apply for this job on the company website.