We continue to invest time, money and energy into making our onsite, hybrid and remote work ... RESPONSIBILITIES: * Serve as the clinical lead for assigned studies, representing Clinical ...
We continue to invest time, money and energy into making our onsite, hybrid and remote work ... RESPONSIBILITIES: * Serve as the clinical lead for assigned studies, representing Clinical ...
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Quick apply
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Remote Study Director information
See salary details
$59.1K is the 25th percentile. Wages below this are outliers.
$45K - $62K
30% of jobs
$62K - $79.1K
9% of jobs
The median wage is $92.2K / yr.
$79.1K - $96.1K
14% of jobs
$96.1K - $113.2K
0% of jobs
$113.2K - $130.2K
0% of jobs
$130.2K - $147.3K
1% of jobs
$147.3K - $164.3K
3% of jobs
$179.6K is the 75th percentile. Wages above this are outliers.
$164.3K - $181.4K
20% of jobs
$181.4K - $198.4K
6% of jobs
$198.4K - $215.5K
9% of jobs
$215.5K - $232.5K
7% of jobs
$45K
$128.4K
$232.5K
How much do remote study director jobs pay per year?
What is the difference between Remote Study Director vs Remote Clinical Project Manager?
| Aspect | Remote Study Director | Remote Clinical Project Manager |
|---|---|---|
| Credentials | Typically requires advanced degrees in life sciences and industry-specific certifications | Requires project management certifications and relevant experience in clinical trials |
| Work Environment | Leads study teams, oversees study design, and ensures compliance remotely | Manages clinical trial projects, coordinates teams, and monitors progress remotely |
| Industry Usage | Commonly used in pharmaceutical, biotech, and CRO sectors | Widely 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 are the key skills and qualifications needed to thrive as a remote study director?
How does a remote study director effectively manage communication and collaboration with dispersed research teams?
What is a remote study director?
What cities are hiring for Remote Study Director jobs?
Cities with the most Remote Study Director job openings:
What states have the most Remote Study Director jobs?
States with the most job openings for Remote Study Director jobs include:
What job categories do people searching Remote Study Director jobs look for?
The top searched job categories for Remote Study Director jobs are:

Associate Director, Clinical Development - Neurology
Carlsbad, CA โข On-site, Remote
Full-time
Posted 23 days ago
Job description
Headquartered in Carlsbad, California, and with offices in Boston, Massachusetts, and Dublin, Ireland, Ionis has been at work for more than three decades discovering medical breakthroughs that have redefined life for people with serious diseases. Weโre pioneers in RNA-targeted medicines, and our platform continues to revolutionize drug discovery and transform lives for patients with unmet needs.ย With multiple marketed medicines and a leading pipeline in neurology, cardiology and select areas of high patient needs, we continue to drive innovation in RNA therapies in addition to advancing new approaches in gene editing to provide greater value to patients and are well positioned financially to deliver on our strategic goals.
At Ionis, we pride ourselves on cultivating a challenging, motivating and rewarding environment that fosters innovation and scientific excellence. We know that our success is a direct result of the exceptional talents and dedication of our employees.ย
With an unprecedented opportunity to change the course of human health, we look to add diverse individuals, skill sets and perspectives to our exceptional team. We continue to invest time, money and energy into making our onsite, hybrid and remote work environments a place where solid and lasting relationships are built and where our culture and employees can thrive.ย
Weโre building on our rich history, and we believe our greatest achievements are ahead of us. If youโre passionate about the opportunity to have meaningful impact on patients in need, we invite you to apply and join us. Experience and contribute to our unique culture while you develop and expand your career!
ASSOCIATE DIRECTOR, CLINICAL DEVELOPMENT - NEUROLOGY
SUMMARY:ย
The Associate Director, Clinical Development โ Neurology provides clinical development leadership and scientific expertise to one or more project teams, supporting the successful design and execution of development plans for Ionisโ investigational assets. Near-term responsibilities focus on leading key aspects of Ionissponsored clinical trials, clinical data analysis and interpretation, communication of project information and risks, and contributions to regulatory submissions, publications, and presentations. Over time, the role may have opportunities to contribute to broader clinical development strategy and clinical trial design.
This position sits within the neurology franchise (including rare diseases). The primary focus will be neurology, including neuromuscular diseases, neurodegenerative diseases, and rare pediatric neurogenetic disorders. This position can be fully onsite, remote, or hybrid. For remote employees, periodic travel to Ionisโ headquarters in Carlsbad is expected, approximately once per quarter.
RESPONSIBILITIES:
- Serve as the clinical lead for assigned studies, representing Clinical Development in internal and external interactions and helping ensure successful execution of a high-priority Phase 3 program by:
- Developing and maintaining excellent working relationships with investigators and clinical trial teams
- Delivering highquality scientific presentations on company technology, investigational agents, and clinical study issues to investigators and site staff
- Providing guidance and/or training for external personnel involved in Ionis clinical studies
- Performing ongoing review of clinical study data and operational progress
- Identifying emerging risks and partnering with the project team to proactively manage and mitigate them
- Lead and/or contribute to the writing and review of key clinical documents for regulatory submissions (e.g., study protocols, Investigatorโs Brochures, IND submissions, Clinical Study Reports).
- Engage internal and external stakeholders (e.g., key opinion leaders, advocacy organizations, regulators) to obtain advice and feedback that informs development plans, trial designs, and study results.
- Communicate project information โ including study progress, risks, plans, and recommendations โ clearly to project teams and Ionis leadership.
- Lead and/or contribute to analysis of clinical trial data and the preparation of manuscripts, abstracts, posters, and presentations.
- Maintain uptodate clinical and technical expertise in the relevant therapeutic areas by reviewing scientific literature, attending key scientific and technical meetings, and partnering with internal medical, research, and commercial teams.
- Contribute to broader department and corporate objectives, as needed.
- Other duties as assigned.
REQUIREMENTS:
- The successful candidate is self-driven and effective both as an individual contributor and a flexible team player. ย They anticipate and identify risks/problems and excel at problem-solving. They bring a practical, handson, โcandoโ and timeconscious approach, motivated by doing the things today that will deliver transformative treatments to patients with high unmet need tomorrow.
- PhD, MD or PharmD with 5+ years of pharma/biotech experience in clinical development
- Experience in neurology, rare diseases, and/or pediatrics is highly desirable
- Significant experience with cross-functional collaboration (e.g., clinical operations, regulatory, stats, data management)
- Experience with protocol/protocol amendment writing and CSR writing
- Experience authoring and/or leading Clinical Study Report (CSR) development. Experience contributing to NDA filings is highly desirable
- Experience leading cross-functional data reviews, experience with elluminate is preferred
- Experience supporting FDA Pre-Approval and BIMO inspections is highly desirable
- Experience managing vendors/committees (e.g., DSMBs) is highly desirable
- Outstanding interpersonal and communication skills, with the ability to flexibly relate to diverse internal and external stakeholders and to build strong, positive relationships across development, research, commercial, and senior leadership
- Ability to thrive in a fastpaced, innovative environment
- Strong attention to detail and quality combined with the ability to make timely decisions and drive execution
- Willingness to engage in thoughtful, interrogative debate around key issues and, when appropriate, to constructively challenge the status quo
Please visit our website,ย http://www.ionis.comย for more information about Ionis and to apply for this position; reference requisition #IONIS004080
Ionis offers an excellent benefits package! Follow this link for more details:ย Ionis Benefits
Full Benefits Link:ย https://ionis.com/careers#:~:text=Highly%20competitive%20benefits
The pay scale for this position is $168,820 to $250,502
NO PHONE CALLS PLEASE. PRINCIPALS ONLY.
Ionis Pharmaceuticals, Inc. and all its subsidiaries are proud to be EEO employers.
About Ionis Pharmaceuticals
Sourced by ZipRecruiter
Industry
Biotechnology research and development
Company size
201 - 500 Employees
Headquarters location
Carlsbad, CA, US
Year founded
1989