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ID: POS08456

Contracts Coordinator (m/f/d)

Pharma & Biotech
Asap
4 months
Monheim Germany
Freelance
K-Recruiting GmbH
Contact:

Karla Pineda

+49 89 1890998-656

karla.pineda@k-recruiting.com

Contracts Coordinator (M/F/D)

 

Tasks:

  • Manage Contract Management Systems (CMS)

  • Handle vendor and site contracts from initiation to archiving, ensuring accurate filing and database updates

  • Coordinate Contract Signatures

  • Distribute and track contracts for internal/external signatures, promote electronic signature solutions

  • Handle Purchase Orders & Contract Distribution

  • Process and distribute POs along with signed contracts to stakeholders

  • Archive and Redact Contracts

  • Scan, store, redact, and archive executed contracts in legal database, especially for audits/inspections

  • Support Site Contracts (including CDAs)

  • Track, scan, and distribute wet ink site contracts; handle courier logistics and database archiving

  • Manage HCP Contracts

  • Draft, review, circulate, and finalize contracts with Health Care Professionals, and ensure SAP/VMD data accuracy

  • Support e-signature training/testing for CRO partners and maintain related training materials and KPIs

  • Prepare documents, organize meetings, maintain department portals, and assist with travel and office needs

  • Adhere to UCB SOPs, ICH/GCP, and regulatory requirements in all documentation and contract processes

  • Identify process inefficiencies and participate in optimizing procedures and system usage.

 

Qualification:

  • Minimum 3 years’ experience in administrative, secretarial, or documentation roles (preferably in pharma/biotech/CRO).

  • High attention to detail and accuracy in handling complex documentation.

  • Excellent English communication skills (written and verbal); German or French is a plus.

  • Strong organizational and time-management skills to manage multiple priorities independently.

  • Proficiency in Microsoft Office (Word, Excel, Outlook, PowerPoint).

  • Understanding of clinical development regulations (FDA, EMA, ICH/GCP) and trial documentation.

  • Experience with legal or paralegal documents is an advantage.

  • Proactive, flexible, and able to handle shifting priorities without close supervision.

  • Strong interpersonal skills to coordinate with global stakeholders and teams.

  • Ability to identify and implement best practices and improve contract coordination processes.

 

Requirements: 

Start: 01.09.2025

Duration: 4 months + extension until 31.12.2026 possible

Capacity: 5 days per week (2 days onsite + 3 days in the office)

Location: Monheim, Germany

 

Have we peaked your interest? Let's go
Contact
Karla Pineda
+49 89 1890998-656
karla.pineda@k-recruiting.com