Referso Jobs

Associate Director, IT Regulatory, Clinical, and Enterprise Systems

Bristol Myers Squibb · Posted Nov 9, 2026

Open

Indianapolis, Indiana, United States +1 more
Full-time · Director
$166K–$221K per year
10+ years

Associate Director, IT Regulatory, Clinical, and Enterprise Systems

Bristol Myers Squibb · Posted Nov 9, 2026

Open

Indianapolis, Indiana, United States +1 more
Full-time · Director
$166K–$221K per year
10+ years

Regulatory Affairs Consultant - Regulatory Generalist

Parexel · Posted Oct 9, 2026

Open

Remote, United States
Remote
5+ years

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Provide end-to-end regulatory support for pharmaceutical development and commercialization programs, including IND/NDA submission management, health authority interactions, and lifecycle maintenance.

Responsibilities

Lead or support IND and NDA submission management
Coordinate health authority meeting requests and correspondence
Prepare and coordinate lifecycle submissions
Conduct regulatory intelligence searches
Prepare global regulatory team materials

Requirements

Bachelor’s degree in a scientific, technical, or related discipline

Skills

regulatory writing submission management IND Module 1 authoring TOC tracking health authority meeting coordination FDA forms drafting regulatory intelligence research RIM

Responsable de projets Affaires Règlementaires Global (H/F)

UPSA · Posted Nov 9, 2026

Open

Agen, Lot-et-Garonne, France +1 more
3+ years

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Responsable de Projet Affaires Réglementaires Globales intervenant sur un périmètre international, principalement centré sur les procédures européennes.

Locations (2)

Agen, Lot-et-Garonne, France
Rueil-Malmaison, Île-de-France, France

Responsibilities

Apporter son expertise réglementaire afin d’obtenir les enregistrements en Europe
Mettre en œuvre les décisions de stratégie réglementaire définies par le Global Regulatory Plan
Rédiger le Module 1 européen et coordonner la constitution du dossier complet
Piloter en autonomie des procédures européennes simples
Coordonner en autonomie les activités de gestion du cycle de vie

Requirements

Bachelor’s degree in science (chemistry, biology, life-science)
Master 2 in Regulatory Affairs
Nice to have: International registration exposure

Skills

Senior Manager, Business Information Architect

Alcon · Posted Nov 7, 2026

Open

Fort Worth, Texas, United States
On-site
Senior
7+ years

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Lead a team of architects to deliver IT system solutions and define enterprise information architecture strategy within Alcon’s Global Process Ownership organization.

Responsibilities

Define enterprise information architecture strategy aligned to global process model
Establish and evolve enterprise-wide taxonomies, ontologies, metadata frameworks, and semantic models
Act as thought leader and advisor to Global Process Owners, Enterprise Architecture, and senior IT and business leadership
Shape governance models balancing standardization with business continuity and agility across regions and functions
Provide architectural oversight for major transformational initiatives and platform evolutions

Requirements

Bachelor’s Degree or Equivalent

Skills

TOGAF ArchiMate BPMN Sparx EA Erwin Collibra Alation

Regulatory Consultant/Sr. Consultant - RIM/Veeva Business Analyst (US timeshift)

Syneos Health · Posted Dec 8, 2025

Open

Remote, India
Remote
Full-time · Senior
8+ years

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Lead regulatory system analysis and stakeholder liaison for RIM/Veeva platforms, ensuring requirements, testing, and training support across global teams.

Responsibilities

Act as primary liaison between Regulatory Operations and IT/Tool Management
Focus on technology enablement and process optimization
Gather and document requirements from key users
Ensure requirements are maintained and updated
Collaborate with DTE and Validation teams

Requirements

Master’s degree

Skills

RIM Veeva system requirement gathering validation user acceptance testing stakeholder management communication

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Legal Records Clerk

Ricoh · Posted Nov 5, 2026

Open

New York, New York, United States
$18–$28 per hour
1+ years

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Oversees and coordinates daily tasks, workflow and special projects within the Records Management Department, including creation, tracking, monitoring, labeling, delivery, closure and storage of active and/or inactive client or firm files.

Compensation

Pay Range: $18.22 - $28.24

Responsibilities

Perform records center operations tasks in accordance with established RIM procedures
Respond to specific requests by searching, locating, retrieving, and delivering records or information through established procedures and delivery systems in a timely manner
Receive files for entry into Records Management System (RMS); review for accuracy and enters data
Sort, classify, and code material for filing, indexing and shelving
Prepare new files within file classification plan, both physical files and electronic files

Requirements

One or more years of college with specialized coursework in administrative management and computer technology
Minimum high school diploma or equivalent; Prefer BA or AA; special training in RM a plus

Skills

RIM EDRM ESI industry best practices

Veeva Vault Product Specialist Clinical

Bayer · Posted Nov 5, 2026

Open

Bangalore, Karnataka, India
5+ years

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Support and manage Veeva Vault applications for Bayer’s clinical operations, ensuring regulatory compliance and driving platform innovation.

Responsibilities

Ensure operation of business‑critical Veeva Vault applications to keep them audit and inspection ready
Collaborate with international stakeholders within business functions
Understand business processes and integration requirements to consult, implement, execute and cross‑collaborate
Guarantee regulatory compliance of solutions
Drive innovation within projects and platform lifecycle management

Requirements

University degree in science or information technology, preferably Master’s degree

Skills

Veeva Platform (Clinical Operations, RIM, etc.)Veeva certification (Platform, eTMF, RIM, etc.)GxP expertise Business process knowledge in Commercial or R&D IT platform/project/product management

Associate Director, IT Regulatory, Clinical, and Enterprise Systems

Associate Director, IT Regulatory, Clinical, and Enterprise Systems

Locations (2)

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Regulatory Affairs Consultant - Regulatory Generalist

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Responsable de projets Affaires Règlementaires Global (H/F)

Locations (2)

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Senior Manager, Business Information Architect

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Regulatory Consultant/Sr. Consultant - RIM/Veeva Business Analyst (US timeshift)

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Legal Records Clerk

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Veeva Vault Product Specialist Clinical

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RIM jobs

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