Senior Regional Study Manager - REMOTE

Jobgether; À distance; EUR 70 000 - 90 000; Plein temps

Résumé du poste

A leading clinical research organization is looking for a Senior Regional Study Manager to oversee clinical studies focused on Infectious Diseases and Vaccines. This role requires a minimum of 6 years of experience in Clinical Trial Management with expertise in managing clinical trials from start-up to database lock. The successful candidate will develop monitoring plans, manage budgets, and liaise with stakeholders. Competitive benefits are offered, including health insurance and flexible benefits.

Prestations

Various annual leave entitlements

Health insurance offerings

Competitive retirement options

Global Employee Assistance Programme

Flexible optional benefits

Qualifications

• Minimum of 6 years of experience in Clinical Trial Management at a CRO or Pharmaceutical Organization.
• Experience managing Infectious Disease and Vaccine studies.
• At least 10+ years of relevant experience in clinical research.

Responsabilités

• Oversee the clinical portion of the budget to ensure efficient resource allocation.
• Develop monitoring plans and tools for effective study oversight.
• Train and mentor Clinical Research Associates (CRAs) to optimize their performance.

Connaissances

Clinical Trial Management

Infectious Diseases knowledge

Vaccines expertise

Stakeholder management

Fluency in English

Formation

Bachelor's degree in health or life sciences

Description du poste

Senior Regional Study Manager - REMOTE

This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Senior Regional Study Manager. In this pivotal role, you will ensure the successful delivery of clinical studies focused on Infectious Diseases and Vaccines. Your substantial expertise will directly impact our clinical activities by managing budgets, developing monitoring plans, and driving enrollment. Additionally, you will liaise with various stakeholders, proactively identify risks, and provide essential reporting to ensure project objectives are met. Join our dynamic team to help shape the future of clinical development.

Accountabilities

• Oversee the clinical portion of the budget to ensure efficient resource allocation.
• Develop monitoring plans and tools for effective study oversight.
• Train and mentor Clinical Research Associates (CRAs) to optimize their performance.
• Drive enrollment and lead study start-up activities, adhering to timelines.
• Review trip reports and implement corrective and preventative action plans as necessary.
• Foster productive relationships with Sponsors, vendors, and cross-functional teams.

Requirements

• A minimum of 6 years of experience in Clinical Trial Management at a CRO or Pharmaceutical Organization.
• Must have experience managing Infectious Disease and Vaccine studies.
• Bachelor's degree in health, life sciences, or relevant fields.
• At least 10+ years of relevant experience in clinical research.
• Preferred: 2+ years of monitoring experience.
• Experience in managing complex or global trials is advantageous.
• Preferred: Experience managing all trial components from start-up to database lock.
• Preferred: Experience in coaching/mentoring other CTMs and leading a team.
• Fluency in English (reading, writing, speaking).

Benefits

• Various annual leave entitlements.
• A range of health insurance offerings to suit you and your familys needs.
• Competitive retirement planning offerings for future savings.
• Global Employee Assistance Programme with 24-hour access to support.
• Life assurance.
• Flexible country-specific optional benefits, including childcare vouchers and discounted gym memberships.