Project Manager Pre-Clinical Studies Job at Argenta (Munich)

New

Project Manager Pre-Clinical Studies

Project Manager for EU CRO Pre-clinical Department, based in offices of San Seba...

Location

Spain , Hondarribia, San Sebastian

Salary:

Not provided

Argenta

Expiration Date

Until further notice

Requirements

University degree in veterinary medicine, animal science, life sciences, or a related field (such as biology, agronomy, or pharmacy)
Master’s degree or specialized training in clinical studies management or monitoring combined with prior experience in a clinical study monitoring environment is considered an asset
Able to familiarize yourself with new tasks and areas of knowledge
Independent and structured way of working
Reliability and high sense of responsibility
Excellent command of written and spoken English
additional foreign language skills are considered an asset
Good teamwork and communication skills
Willingness to travel for business (approx. 30% of working time)
Driver‘s license class B

Job Responsibility

Complying with the responsibilities as defined by VICH GCP (Veterinary Good Clinical Practice), GLP (Good Laboratory Practice), and all applicable regulatory requirements
Advising clients on study design and placement of GCP/GLP field and laboratory studies in Europe and internationally
Building, coordinating and leading multidisciplinary teams across individual studies, including selection and training of investigators, study set-up activities
Monitor activities during the study, including communication with investigators and laboratories, on site visits/travel to study sites (e.g., veterinary clinics, farms), tracking of study cases (including enrolment, adverse events (AEs), deviations, and protocol compliance), supervision of laboratory diagnostic activities, drug accountability, tracking of financial aspects of study sites (checking and approving invoices)
Continuous quality control of the study data collected within the scope of the study and their evaluation in the context of GCP/GLP quality standards
Preparation/review of study protocols and final study reports in the context of GCP/GLP quality standards
Managing project budgets and reporting to middle management

What we offer

Detailed introduction to your field of work
Challenging field of activity contributing to the availability of animal health products
Work in an international team
Family-friendly environment
Options for continuous education
Very positive and collegial team atmosphere in San Sebastian

Fulltime

Senior Clinical Scientist

The Senior Clinical Scientist role is suited to scientifically minded candidates...

Location

United States , Salt Lake City

Salary:

Not provided

Blackrock Neurotech

Expiration Date

Until further notice

Requirements

Ph.D. in Neuroscience, Biomedical Engineering, or a related field
Proven expertise in experimental design, data analysis, and scientific communication
Demonstrated experience working across pre-clinical and clinical research settings, with the ability to translate study objectives into executable protocols and comparable datasets across settings
Experience developing and/or executing acute and/or intraoperative electrophysiology studies
Strong analytical skills and proficiency with statistical software and data visualization tools, including analysis of electrophysiology and device performance data
Excellent written and verbal communication skills
Ability to work independently and as part of a collaborative team

Job Responsibility

Lead and manage clinical research projects, collaborating with pre-clinical and multidisciplinary teams, and ensuring alignment with company goals and regulatory requirements
Partner between clinical and pre-clinical teams to develop and execute acute and intraoperative electrophysiology studies, including defining endpoints, coordinating execution workflows, and ensuring high-quality data acquisition
Support and/or coordinate hardware testing in the context of acute/intraoperative clinical studies (e.g., test planning, setup verification, troubleshooting, and structured capture of outcomes to inform development decisions)
Analyze and interpret complex data sets, providing actionable insights to guide BCI development
Collaborate with cross-functional teams, including engineering, regulatory, and clinical affairs, with emphasis on bridging clinical and pre-clinical stakeholders to align study execution and hardware testing needs
Prepare and present scientific reports, publications, and presentations to internal and external stakeholders
Stay current with advancements in neurotechnology and related fields to inform research strategies
Mentor and provide guidance to junior scientists and other team members

Fulltime

New

Senior Product Development Manager

At Argenta, we’re more than a company — we’re a global team, dedicated to health...

Location

United States , Shawnee, Kansas

Salary:

Not provided

Argenta

Expiration Date

Until further notice

Requirements

10+ years or greater in veterinary drug development
Clinical Research Associate experience or equivalent experience and training
Experience and skills necessary to monitor a study
Results oriented. Defines and plans priorities well
Effectively manage client and stakeholder expectations through relevant communication
Comfortable balancing shifting priorities as required to meet business needs
A collaborative working style to be able to lead and motivate people at all levels and across all functions in an organization
Strong analytical thinking and problem-solving skills
Capable of working in a changing environment and under pressure
Effectively present information and concepts, in both written and oral formats clearly and concisely

Job Responsibility

Supports the Americas CRO business (regulatory to pre-clinical to clinical service) needs of Argenta Molecule to Market, and Risk/Mitigation plans
Effectively manage the product development requirements (pre-clinical and clinical projects) of internal and external projects
Demonstrates an awareness of current regulations, guidance's, and the animal drug development process, while maintaining a flexible and creative mindset to work through product development challenges
Contribute to the development of business strategies to increase profitability and grow the business to create value
Manage development projects or key development project areas from initial conversations to live-phase study activities to close-out / final study report signatures to tracking overall timelines and budgets for study activities
Coordinates selection of the vendor(s) for study protocol conduct &/or laboratory requirements and activities including the provision of necessary supplies required by the study protocol
Provides oversight to ensure tasks are completed correctly and on time (i.e. oversight in the tracking of adverse events (AEs) encountered in the study and ensures that all serious AEs and non-serious AEs are communicated appropriately to the Sponsor)
Coordinates the creation of materials and documentation for the study, and QA resources, as required
Directs and provides oversight of investigational veterinary product/control product inventory, accountability, labelling, regulatory documentation/notifications, and shipment of drug supplies to/from the Sponsor and study sites

Fulltime

Director of Quality Assurance, Clinical

Responsible for leading in the development, implementation and maintenance of QA...

Location

United States , Berkeley

Salary:

220000.00 - 235000.00 USD / Year

Caribou Biosciences

Expiration Date

Until further notice

Requirements

Undergraduate or graduate degree(s) in Biological Sciences, Chemistry, or related Science discipline
At least 15 years of experience in clinical quality assurance (GCP, GLP and PV) in cell & gene therapy/biotechnology and/or pharmaceutical industry
Experience working in biologics is strongly preferred
Subject Matter Expert (SME) working knowledge on current interpretation/implementation of United States Code of Federal Regulations, ICH Guidelines and other local government regulatory requirements governing clinical research
Proven track record in developing and implementing quality systems and processes in a clinical setting
Expertise in creating and executing audit plans outlining all service providers (vendor) audits, clinical investigator site audits, CSV audits and process audits
Advanced knowledge of Quality Assurance principles, concepts, industry practices, and standards
Prior GLP experience with quality oversight and auditing studies/vendors (preferred)
Excellent verbal and written communication skills
Ability to lead cross-functional teams and independently prioritize work

Job Responsibility

Compliance Oversight: Ensure that all clinical trial activities comply with guidelines and international regulations (e.g., ICH-GCP and ICH-PV), and applicable laws
Documentation Review: Conduct thorough reviews of study-related documentation, including protocols, investigator brochures, informed consent forms, and CSRs, to verify compliance with GCP requirements
Provide Clinical Quality Assurance (GCP) strategic and technical leadership and Subject Matter Expertise (SME) to clinical study teams
Partner with the teams to effect appropriate and timely documentation of quality event management, including CAPA plans in support of product pipeline
Plan and oversee activities in support of regulatory submissions and inspections
Lead GCP Inspection Readiness efforts, ensure implementation and prepare internal and external teams for Pre-Approval Inspections (PAI)
Implement, monitor, and promote best practices of all Quality Assurance Systems to ensure compliance with relevant FDA, EU and ROW regulations/directives/requirements and ICH guidelines
Quality Management System (QMS): Maintain and enhance Caribou’s QMS by implementing processes and procedures that ensure consistent adherence to GCP, GLP and PV standards throughout the clinical trial lifecycle
Develop and implement the appropriate suite of Standard Operating Procedures (SOPs), quality manuals, policies, and other related quality documents
Ensure that these systems are effectively communicated, understood, and followed by relevant stakeholders

What we offer

Comprehensive compensation package, which includes competitive salary, bonus, and equity for all employees
Generous paid vacation time, in addition to company-observed holidays
Excellent medical, dental, and vision insurance
401(k) retirement savings plan, which includes matching employer contributions
Employee stock purchase plan (ESPP)
Tuition reimbursement program

Fulltime

Pathology Operations Director – PreClinical CRO

Manage team of study coordinators for pre-clinical drug development. This positi...

Location

United States

Salary:

Not provided

AchieveBio

Expiration Date

Until further notice

Requirements

BS in life science discipline
5+ years study coordination experience in the Pre-Clinical Space
2+ years supervisory/leadership experience
QC experience preferred
Ability to build strong teams, and develop individual contributors through mentoring and training

Job Responsibility

Manage, train and mentor team of 5-6 study coordinators
Oversee scheduling and execution of project work and QC
Collaborate with Study Directors, Project Managers and Proposals teams to ensure timely and cost effective completion of studies
Develop and update SOPs and QC processes

What we offer

Relocation assistance available

R&D Assistant

As an R&D Assistant, you will support and contribute to Flen Health's research a...

Location

Belgium , Kontich

Salary:

Not provided

Flen Health GmbH

Expiration Date

Until further notice

Requirements

Bachelor’s or Master’s degree in pharmaceutical and biological techniques or equivalent by experience
initial skin pharmaceutical product knowledge
biological and chemical lab techniques knowledge
good command of MS Office
digital savviness related to lab management, project planning and research-related software are an asset
fluent in English, both written and spoken

Job Responsibility

Support research activities on innovative treatments of wound and skin disorders using microbiology techniques
pre-sequencing, post-sequencing, and other biotechnology techniques and galenics
contribute to the development of new and/or renewed (pharmaceutical) formulations for Flen Health products and execute pre-clinical studies according to planning
test the existing and new Flen Health products and ensure that they follow design and development project planning
ensure Laboratory maintenance and control of equipment and contribute to administrative tasks related to lab and R&D testing
assist in coordinating and monitoring analytical, chemical, physical, or biological tests that are outsourced to third parties

What we offer

Excellent working conditions
innovative and inspiring work environment
independent project work & responsibilities within a professional team
career prospect
learning and development opportunities
competitive remuneration according to experience
flexible working ecosystem
enthusiastic colleagues
attractive remuneration package

Fulltime

New

Senior Administrative Assistant

We are looking for a dedicated and experienced Senior Administrative Assistant t...

Location

United States , Bedford Park

Salary:

25.00 USD / Hour

Robert Half

Expiration Date

Until further notice

Requirements

Minimum of 3 years of experience in an administrative or project support role
Advanced proficiency in Microsoft Office Suite, including Word, Excel, PowerPoint, and Outlook
Ability to work independently and solve problems proactively with minimal supervision
Proven skill in managing calendars, scheduling meetings, and organizing travel arrangements
Strong organizational skills and meticulous attention to detail
Excellent written and verbal communication skills, with the ability to adapt to different contexts
Experience with Microsoft Teams for collaboration and communication
Quick learner who can adapt rapidly to new systems, processes, and tasks

Job Responsibility

Coordinate and provide administrative support to committees, workgroups, and projects, ensuring smooth operations and timely completion
Utilize advanced skills in Microsoft Word, Excel, PowerPoint, and Outlook to create, edit, and manage documents, presentations, and spreadsheets
Independently research and resolve challenges, demonstrating resourcefulness and self-direction
Manage calendars, schedule meetings, and organize conference calls with precision and efficiency
Arrange travel logistics and prepare documentation related to import and export processes
Plan and execute events, including badging and other logistical tasks
Maintain strong attention to detail while managing high-volume workloads and tight deadlines
Write, interpret, and communicate information effectively, adapting to various audiences
Use Microsoft Teams for collaboration and task coordination
Ensure projects are completed accurately and on time, showcasing excellent organizational skills

What we offer

medical
vision
dental
life and disability insurance
401(k) plan

New

Yard Sales Assistant

Join our team at RGB, a respected independent builder’s merchant serving the Sou...

Location

United Kingdom , Exeter

Salary:

Not provided

Grant and Stone Limited

Expiration Date

March 12, 2026

Requirements

Yard Experience
Experience loading & unloading goods (advantageous)
Counter balance licence (advantageous)
Builders merchants experience (advantageous)
Excellent customer service skills
Excellent communication skills
The ability to communicate at all levels
Self-motivated with a can-do attitude
Strong team player who works as part of a team and independently

Job Responsibility

Handle and maintain yard stocks
Load and unload both customer, supplier and company delivery vehicles
Serve customers, advise on stock, availability and product ranges
Ensure the premises are kept to a high standard to comply with Health & Safety regulations
Maintain a clean and tidy yard and working area

What we offer

Competitive salary
Pension scheme and paid holidays
Supportive team and positive work environment
Career development and training
Staff discount on building materials
Employee assistance program
Perks Membership (Discounts available in a variety of retailers)
Branded Uniform

Fulltime

Project Manager Pre-Clinical Studies

Argenta

Location:
Germany , Munich

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
February 14, 2026

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Location:Germany , Munich

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Contract Type:Not provided

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Job Description:

Job Responsibility:

Requirements:

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Job Posted:
February 14, 2026