Offer summary

Qualifications:

Master's degree or higher in Life Science field preferred., Fluent in English with strong communication skills., Minimum of 5 years' experience in Clinical Research, including project management., Familiarity with eClinical systems and early phase clinical trials is advantageous..

Key responsabilities:

Manage and coordinate cross-functional teams and third-party vendors for clinical trials.

Oversee project budgets, including tracking and forecasting.

Develop and implement clinical project plans and lead project teams.

Serve as the primary contact for sponsors, providing regular project updates.

Job description

Future Opportunity: Clinical Project Manager

At Biomapas, we are continuously expanding our Clinical Trial projects, and this means we are always on the lookout for talented Clinical Project Managers to join our team. While we may not have an immediate opening, we are proactively seeking experienced Clinical Project Managers who see themselves as part of our growing team. If you are passionate about clinical research, project leadership, and working in an international environment, we invite you to submit your application today. We will get in touch when a suitable opportunity arises!

As a Clinical Project Manager, you will be responsible for planning, organizing, and overseeing the execution of clinical trials, ensuring projects are completed on time, within budget, and in compliance with industry regulations

Location: Europe (Fully Remote)

Responsibilities:

· Manage and co-ordinate efforts of cross-functional teams, including 3rd party vendors, to support milestones achievement and compliance with company procedures and regulations

· Manage project budget including tracking, forecasting, identification of out-of-scope items and participation in the preparation of change orders

· Develop clinical project plans (project management, communication, monitoring and etc.)

· Lead clinical project team (internal resources and third parties/vendors)

· Serve as the first point of contact for the sponsor providing regular updates on the project’s status

· Identify quality issues, implement appropriate corrective and preventive action plans

· Provide input and/or develop proposals for new projects

· Support business development by preparation and participation in bid defense meetings

Requirements

· Preferable Master or higher degree in Life Science field

· Fluent English language

· 5 years’ experience in Clinical Research field (Healthcare, Sponsor organization or CRO) with the responsibilities including organization and management of clinical projects

· Project management and study team management experience

· Experience in early phase clinical trials and oncology field is an advantage

· Reporting, time and risk management skills

· Familiarity with standard business and eClinical systems (CTMS, EDC, IXRS, eTMF and project planning tools)

Benefits

· International team and environment

· Performance based annual bonus

· Remote Work, workation & Flexibility

· Health & Wellbeing – wellness initiatives

· Professional growth and development in the Life science industry

· Team Culture – Team buildings, global meetings, and B Active events.

· Comprehensive Insurance - Personal accident, business trip coverage, and additional health insurance.

UAB "Biomapas" (“Biomapas”) processes personal data of job applicants for the purpose of selecting job candidates. More information about the processing of personal data is available online at https://www.biomapas.com/privacy-policy/.

By submitting your CV to Biomapas, you agree to your personal data processing by Biomapas within the database of Human Resources database of Biomapas

Required profile