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Remote Study Director Jobs in California (NOW HIRING)

Director, Clinical Science

San Diego, CA ยท On-site +1

$84K - $115K/yr

San Diego, USA- Remote Be a part of a global team that is inspired to make a difference in the ... The position will work with cross-functional multidisciplinary study teams on clinical trial design ...

Director, Clinical Science

San Diego, CA ยท On-site +1

$236K - $255K/yr

Knowledge of oncology drug development and clinical trial processes, study design, statistics and ... Remote permitted upon approval, with ability to travel up to 25% for meetings or site visits as ...

Director, Clinical Science

San Diego, CA ยท On-site +1

$236K - $255K/yr

Knowledge of oncology drug development and clinical trial processes, study design, statistics and ... Remote permitted upon approval, with ability to travel up to 25% for meetings or site visits as ...

Review and edit study protocols and reports to ensure scientific rigor, regulatory compliance (GLP ... Remote work is an option. * We are passionate about our culture! Our Tarsans live our values of ...

Showing results 41-60

Remote Study Director information

What is a remote study director?

A Remote Study Director is a professional responsible for overseeing and managing research studies or clinical trials from a remote location, rather than being physically present at the research site. Their duties include designing study protocols, coordinating with research teams, monitoring study progress, ensuring regulatory compliance, and maintaining data quality. Remote Study Directors use digital tools to communicate, track milestones, and manage documentation, making it possible to lead studies efficiently without being on-site. This role is common in fields like clinical research, pharmaceuticals, and academic studies, especially as remote work becomes more prevalent.

What are the key skills and qualifications needed to thrive as a remote study director?

To thrive as a Remote Study Director, you need a background in life sciences or a related field, experience in research project management, and a thorough understanding of study protocols. Familiarity with project management software, data collection tools, and compliance systems such as Good Clinical Practice (GCP) is typically required. Strong organizational, communication, and leadership skills help manage virtual teams and ensure studies stay on track. These competencies are critical for coordinating complex research projects remotely and ensuring regulatory compliance and data integrity.

How does a remote study director effectively manage communication and collaboration with dispersed research teams?

As a Remote Study Director, maintaining clear and consistent communication is essential for coordinating research activities and ensuring project milestones are met. You'll typically use a combination of video conferencing, project management platforms, and shared digital documentation to facilitate regular updates and resolve issues in real time. Establishing structured check-ins and transparent reporting processes helps keep team members aligned and informed, while also allowing you to promptly address challenges such as time zone differences or varying team member availability. Building trust and fostering a collaborative virtual environment are key to achieving successful study outcomes.

What is the difference between Remote Study Director vs Remote Clinical Project Manager?

AspectRemote Study DirectorRemote Clinical Project Manager
CredentialsTypically requires advanced degrees in life sciences and industry-specific certificationsRequires project management certifications and relevant experience in clinical trials
Work EnvironmentLeads study teams, oversees study design, and ensures compliance remotelyManages clinical trial projects, coordinates teams, and monitors progress remotely
Industry UsageCommonly used in pharmaceutical, biotech, and CRO sectorsWidely used in clinical research organizations and pharmaceutical companies

The Remote Study Director focuses on overseeing entire clinical studies, ensuring scientific and regulatory compliance, while the Remote Clinical Project Manager manages project timelines, budgets, and team coordination. Both roles require industry experience and often work remotely within the clinical research industry, but their core responsibilities differ in scope and focus.

What job categories do people searching Remote Study Director jobs in California look for?

The top searched job categories for Remote Study Director jobs in California are:

What cities in California are hiring for Remote Study Director jobs?

Cities in California with the most Remote Study Director job openings:

Director, Pharma Delivery Operations

Redwood City, CA โ€ข On-site, Remote

$215K - $245K/yr

Full-time

Retirement

Re-posted 9 days ago


Job description

About N-Power Medicine


N-Power Medicine aims to establish a new paradigm in drug development by reinventing the ‘how’ and transforming clinical trials through Prospective External Control Arms, better integration with clinical practice, and broader participation by physicians and patients.  We are building an exceptional multi-disciplinary team with diverse expertise spanning healthcare, engineering, technology and regulatory, and with people who share our core value of Empowering Community through generosity, curiosity and humility.  We are working with urgency to bring better therapies to patients faster. 


Position Overview


N-Power Medicine is hiring a Director, Pharma Delivery Operations position based in Redwood City, CA.  As the Director, Pharma Delivery Operations, you will be responsible for the successful execution and delivery of life sciences contracts. This role requires a highly organized individual who excels at client management, cross-functional collaboration, and bringing teams together to ensure seamless contract delivery. You will serve as the primary point of contact for executed contracts, driving operational excellence while maintaining strong client relationships.


This is a hybrid role; Bay Area preferred, remote considered for the right candidate.


Role Objectives and Responsibilities


Client & Contract Management (Pharma Delivery)


  • Own the Pharma/Biotech client relationship for an assigned portfolio of contracts, serving as the primary point of escalation for delivery risks

  • Ensure teams fully understand contract scope, timelines, and deliverables, and translate contract terms into executable operational plans by leading cross-functional coordination efforts, bringing together teams from Clinical Operations, Epidemiology, Biostatistics, Product, Engineering, Data Science, and other internal stakeholders to deliver on contract commitments.

  • Drive on-time, on-budget delivery across the portfolio; proactively identify and resolve risks before they reach the client

  • Partner with sales/business development on renewals, scope changes, and expansion opportunities informed by delivery performance


Portfolio & Reporting


  • Design and maintain KPI tracking at the study and portfolio level; deliver clear, concise reporting to leadership and clients

  • Identify systemic operational gaps or risks across studies and drive process improvements

  • Standardize documentation, communication cadences, and escalation pathways across the team's studies


People Leadership


  • Manage, coach, and develop a team of Delivery Operations Managers setting clear goals and providing regular performance feedback

  • Build team-level processes for knowledge sharing, escalation, and cross-coverage across studies

  • Represent the team's work and needs to the senior organization leadership


Education, Experience, Behavioral Competencies, & Skills


Required Qualifications


  • Bachelor's degree required; advanced degree in business, life sciences, or related field preferred

  • 8 - 12 years of experience in clinical operations, delivery/program management, or client operations within healthcare, life sciences, or clinical research

  • Prior people management experience, including hiring, coaching, and performance management

  • Prior experience managing client interactions and client operations

  • Working knowledge of GCP, IRB processes, and clinical trial regulatory requirements

  • Demonstrated ability to manage complex, multi-stakeholder contracts or studies simultaneously

  • Strong analytical and reporting skills; comfortable building and presenting portfolio-level metrics

  • Excellent written and verbal communication skills, with experience managing client relationships directly


Preferred Qualifications


  • Experience in a sponsor, CRO, or healthcare technology environment

  • Track record scaling operational processes in a high-growth or ambiguous environment

  • Familiarity with project management or CRM tools (e.g., Jira, Hubspot, or similar)

  • Experience with clinical biospecimen management, imaging, registry, or observational study operations a plus

 

Travel Requirements 


Up to 10% of time required to travel in role (out of 100%)

Pay Information


The expected salary range for this position is $215,000 to $245,000.  Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. N-Power Medicine (NPM) offers equity at hire as well as a discretionary annual bonus which may be available based on Company performance. This position is eligible for company benefits.


More About Us:

We are a mission-driven, well-funded, rapidly growing company, eager to attract passionate professionals offering a highly attractive compensation package with a balanced and flexible work environment, competitive industry benefits as well as a 401K plan and other great company “perks.”

We are an Equal Opportunity Employer and value diversity at our company. We do not discriminate based upon race, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.

Covid-19 Policy –  The Company is committed to providing and maintaining a safe workplace, and to safeguard the health and well-being of our employees, families, visitors, and the community. While vaccination remains one of the most important tools in advancing the health and safety of employees and promoting the efficiency of workplaces, we are now in a different phase of our response when these measures are no longer necessary. We currently do not have mandatory COVID-19 vaccination requirements for our employees and contractors, as the COVID-19 public health emergency has ended. However, there are certain N-Power Medicine employees and contractors who, based on their role, will be required to continue to follow our 2021 COVID-19 vaccination and other requirements as mandated by N-Power Medicine’s partners they serve. We reserve the right to modify or amend our corporate policy at any time.

Applicants must be currently authorized to work in the U.S. on a full-time basis. The Company will not sponsor applicants for work visas.

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.