ZipRecruiter

Log In

2

Director Biotech Remote Jobs in Missouri (NOW HIRING)

Jobgether

... biotechnology environment. You'll collaborate across North America, Europe, and Israel, working ... Benefits: * Full-time, remote position with a flexible working environment. * Opportunity to work ...

New

Danaher

Regional Sales Manager

Saint Louis, MO · On-site +1

$252K/yr

... biotechnology? At Mammotome, one of Danaher's 15+ operating companies, our work saves lives-and we ... You will be a part of the field sales organization and report to the Senior Director, National ...

Danaher

Senior Service Sales Specialist

Kansas City, MO · On-site +1

$109K - $128K/yr

... and biotechnology? At Leica Biosystems, one of Danaher's 15+ operating companies, our work saves ... This position reports to the Director, Service Business Operations and operates within the North ...

Danaher

Senior Service Sales Specialist

Saint Louis, MO · On-site +1

$109K - $128K/yr

... and biotechnology? At Leica Biosystems, one of Danaher's 15+ operating companies, our work saves ... This position reports to the Director, Service Business Operations and operates within the North ...

All JobsBiotech JobsDirector Biotech Remote JobsDirector Biotech Remote Jobs in Missouri

Director Biotech Remote information

What does a director biotech remote do?

A Director Biotech Remote is a senior leadership role responsible for overseeing biotechnology projects and teams while working remotely. They manage research and development strategies, ensure compliance with industry regulations, and drive company goals in areas like drug discovery, clinical trials, or product development. The director collaborates with cross-functional teams, sets project priorities, and communicates progress to stakeholders. Remote directors use digital tools to lead effectively, ensuring productivity and alignment despite the physical distance from their teams.

What are the key skills and qualifications needed to thrive as a director biotech remote, and why are they important?

A Director Biotech (Remote) needs advanced expertise in life sciences, leadership experience, and often a PhD or related degree, with a strong track record in biotechnology project management. Familiarity with laboratory information management systems (LIMS), data analytics platforms, and regulatory compliance (such as FDA or EMA guidelines) is crucial, along with certifications like PMP or Six Sigma being advantageous. Outstanding communication, strategic thinking, and team leadership skills help bridge remote teams and drive innovation. These competencies ensure effective oversight of biotech operations, regulatory adherence, and the successful execution of complex projects in a distributed work environment.

What are some common challenges faced by directors in remote biotech roles, and how can they be effectively managed?

Directors in remote biotech positions often face challenges such as coordinating cross-functional teams across different time zones, maintaining clear communication, and ensuring regulatory compliance from a distance. Effective management involves leveraging digital collaboration tools, setting clear expectations, and fostering a culture of transparency and accountability. Regular virtual meetings and proactive relationship-building with both internal and external stakeholders are also critical for driving project success and team cohesion in a remote environment.

What is the difference between Director Biotech Remote vs Senior Research Scientist?

AspectDirector Biotech RemoteSenior Research Scientist
CredentialsAdvanced degrees (PhD/MSc), leadership experienceTypically PhD or MSc in relevant field
Work EnvironmentRemote leadership, strategic planningLaboratory or office-based research
Employer & Industry UsageBiotech companies, pharma firms, research institutionsResearch labs, biotech companies, academia
Search & Comparison IntentUnderstanding leadership roles in biotechResearch roles, scientific expertise

The main difference between a Director Biotech Remote and a Senior Research Scientist lies in their responsibilities and work environment. The Director typically oversees teams remotely, focusing on strategic and leadership tasks, while the Senior Research Scientist conducts hands-on research in labs. Both roles require advanced degrees, but the Director emphasizes leadership and remote work, whereas the Senior Research Scientist centers on scientific research and experimentation.

What are popular job titles related to Director Biotech Remote jobs in Missouri?

For Director Biotech Remote jobs in Missouri, the most frequently searched job titles are:

What job categories do people searching Director Biotech Remote jobs in Missouri look for?

The top searched job categories for Director Biotech Remote jobs in Missouri are:

What cities in Missouri are hiring for Director Biotech Remote jobs?

Cities in Missouri with the most Director Biotech Remote job openings:

Director Biotech Remote jobs near you

Director/Senior Director, Safety-PV Operations Lead

Jobgether

Remote

Full-time

Posted 2 days ago

New

Job description

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Director/Senior Director, Safety-PV Operations Lead based in Netherlands.

This is a senior pharmacovigilance leadership role responsible for shaping and executing global safety operations across late-stage clinical development and commercialization activities.
You'll own the operational safety model, ensuring it remains lean, agile, compliant, and capable of supporting complex global programs.
The role combines strategic oversight with hands-on execution, including vendor management, safety documentation, signal management, and regulatory readiness.
You'll work closely with medical safety, regulatory, quality, biostatistics, medical writing, and external partners to maintain high standards of patient safety and compliance.
The position offers significant influence over safety processes, governance, systems, and operational strategy within a fast-moving biotechnology environment.
You'll collaborate across North America, Europe, and Israel, working with distributed teams and external vendors in a highly flexible setting.
This is an opportunity to make a meaningful contribution to global drug development while helping build scalable safety capabilities for future commercialization.

Accountabilities:
  • Provide strategic direction for global safety and pharmacovigilance operations, ensuring an effective, compliant, and cost-efficient operating model.
  • Develop, maintain, and oversee safety operational documents and agreements with external partners, including Joint Operating Guides, Safety Management Plans, and Safety Data Exchange Agreements.
  • Coordinate the development of core safety documents, including DSURs, Reference Safety Information within Investigator's Brochures, CCSI, and RMP/REMS materials, in collaboration with Regulatory Affairs.
  • Coordinate high-quality safety outputs with Biostatistics, Quality Assurance, medical writing, and external vendors.
  • Support ongoing safety surveillance, including signal management, risk assessment, and periodic safety reporting.
  • Serve as the primary point of contact for safety vendors and CROs, managing work orders, budgets, deliverables, administrative requirements, and overall performance.
  • Monitor vendor safety KPIs, ensure adherence to Safety Management Plans, and oversee implementation of required risk mitigation measures.
  • Establish and maintain safety procedures, governance models, and SOPs appropriate to the stage of product development and future commercialization.
  • Partner with Quality Assurance to ensure appropriate safety training is implemented, completed, and documented.
  • Work closely with global medical safety leadership and represent safety operations in governance and decision-making forums.
  • Collaborate with Regulatory Affairs, PV Quality Assurance, medical writing, and other internal functions to align safety expectations and maintain regulatory compliance.
  • Represent safety operations in interactions with development and commercialization partners.
  • Participate in clinical trial teams and expanded-access or compassionate-use programs as required.
Requirements:
  • Advanced degree such as a PhD, PharmD, MSc, or equivalent in a life-science or medical discipline.
  • At least 5 years of experience in a comparable pharmacovigilance or safety operations leadership role, with experience across both small biotechnology and larger pharmaceutical organizations.
  • Demonstrated experience supporting late-stage clinical development, initial commercialization, and compassionate-use or expanded-access programs.
  • In-depth knowledge of global pharmacovigilance and safety requirements, including GVP and 21 CFR Part 11.
  • Strong understanding of pre- and post-marketing safety requirements and global regulatory expectations.
  • Experience creating and maintaining CCSI and initial RMP/REMS documentation.
  • Experience interacting with regulatory authorities such as the FDA, Health Canada, and EMA/PRAC regarding risk management and risk minimization activities.
  • Practical experience with safety systems and tools, including Argus, Veeva, and MedDRA.
  • Proven ability to manage CROs, vendors, and other external partners while maintaining quality, timelines, budgets, and compliance.
  • Strong written and verbal communication skills, with the ability to work effectively across technical, clinical, regulatory, and operational audiences.
  • Hands-on, solution-oriented approach with the willingness to take ownership and drive critical documentation and processes to completion.
  • Ability to work independently while collaborating effectively within a distributed, cross-functional organization.
  • Willingness to travel occasionally for face-to-face meetings and collaborate across North American, European, and Israeli time zones.
Benefits:
  • Full-time, remote position with a flexible working environment.
  • Opportunity to work across international teams spanning Europe, North America, and Israel.
  • Flexible schedule designed to support collaboration across multiple time zones.
  • Opportunity to contribute to late-stage clinical development and future commercialization programs.
  • Significant ownership and strategic influence over global safety and pharmacovigilance operations.
  • Occasional travel for in-person meetings and team collaboration.
  • Inclusive and collaborative environment focused on meaningful patient impact.
  • Equal opportunity workplace committed to diversity, inclusion, and a welcoming culture.
How Jobgether works:
We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team.
We appreciate your interest and wish you the best!
 Why Apply Through Jobgether? 
 
Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time.
 
 
#LI-CL1
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
apply for this job

Apply