REGULATORY AFFAIRS JR ANALYST Consultant

Reposted 14 Days Ago
Be an Early Applicant
Hiring Remotely in Colombia
Remote
Junior
Pharmaceutical
The Role
The Regulatory Affairs Jr Analyst Consultant ensures regulatory data compliance, supports submission and approvals of market licenses, organizes tasks, and communicates with stakeholders.
Summary Generated by Built In

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds….

ClinChoice is searching for a Regulatory Affairs Associate Consultant for 12 months Contract with possibility of extension to join one of our clients.

ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts.  


JOB DESCRIPTION

Job Title

REGULATORY AFFAIRS JR ANALYST Consultant

Job Summary

Ensures regulatory data is compliant in all databases. Execute activities such as preparation of labels, update of systems and archives, review regulatory data in internal and external databases. Support submission and approvals of market licenses including changes, renewals and establishment registrations. Organize and balance a multitude of activities simultaneously.

Scope

 

Major  Roles and Responsibilities

  • Execute post-approval activities such as review of databases, preparation of communications to stakeholders.
  • Update systems with regulatory data and documents.
  • Review labels compliance in internal system.
  • Execute submission of changes, amendments, rectifications and renewals in timely manner with guidance.
  • Provide assistance with establishment registration licenses.
  • Request and follow-up of documentation to prepare registration dossiers.
  • Supports regional team on product submissions schedules, prioritization, and pipeline management with guidance.
  • Act as a point of contact for stakeholders to support business plans and regulatory needs.
  • Support projects as representative of the subject/country.
  • Organize the archive of the area.
  • Organize team meetings and elaborate agenda and minutes.
  • Support compulsory certification activities.

Competencies

  • Planning and Organizing skills
  • Analytical capability and investigative skills
  • Prioritizes work to meet deadlines
  • Understands the importance of the adherence to compliance
  • Ability to manage complex data with excel spreadsheets are desirable

GLP Behaviors

  • Collaboration and teaming
  • Intellectual curiosity
  • Sense of Urgency

·       Accountability

·       Integrity & Credo-based Actions

  • Self Awareness & Adaptability

Experience/ Qualification  Requirements

  • Desirable some experience working in Regulatory Environment (and/or training or equivalent combination of education and experience), preparing submissions for Colombian Health Authorities.

·       Desirable experience in health care companies.

Education Requirements

·       A Bachelor’s Degree in Engineering, Pharmacy or other life science: Can be a person with related experience and/or training or equivalent combination of education and experience. Intermediate writing and reading skills in English. 



Skills Required

  • Some experience working in Regulatory Environment preparing submissions
  • A Bachelor's Degree in Engineering, Pharmacy or other life science
  • Intermediate writing and reading skills in English

ClinChoice Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about ClinChoice and has not been reviewed or approved by ClinChoice.

  • Flexible Benefits Flexible arrangements, including telecommuting and flextime with no core hours in some regions, are highlighted for many roles. Feedback suggests flexibility is commonly available but depends on role and location.
  • Leave & Time Off Breadth Vacation, personal, and sick days are part of the core package, with some markets granting paid leave from the date of hire. Feedback suggests time off is standard-to-decent across locations, though specifics vary.
  • Healthcare Strength Health coverage is positioned as a core benefit, with some accounts describing overall benefits as full or good. In the U.S., healthcare sits within a conventional CRO package alongside medical, dental, and vision.

ClinChoice Insights

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The Company
HQ: Fort Washington, PA
5,000 Employees
Year Founded: 1995

What We Do

ClinChoice is a global full-service Contract Research Organization (CRO) specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies, aiming to accelerate the development and commercialization of innovative drugs and devices.

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