Is the Director, Head of Medical Writing role at Bluerocktx remote?

The Director, Head of Medical Writing role at Bluerocktx is an on-site position located in Cambridge, Massachusetts.

What is the salary range for Director, Head of Medical Writing at Bluerocktx?

The salary range for the Director, Head of Medical Writing position at Bluerocktx is USD 198,000 - 233,300 per year.

How do I apply for the Director, Head of Medical Writing position at Bluerocktx?

You can apply for the Director, Head of Medical Writing position at Bluerocktx directly through HireHere. Click the "Apply" button on the job listing to be taken to the application page.

Director, Head of Medical Writing

$198k - $233k USD

BluerocktxCambridge, Massachusetts2h ago

Who is BlueRock?

BlueRock Therapeutics LP is a clinical stage cell therapy harnessing the power of cell therapy to create a pipeline of new medicines for people suffering from neurological and ophthalmic diseases. Two of our novel investigational cell therapies, bemdaneprocel (BRT-DA01) for the treatment of Parkinson’s disease and OpCT-001 for the treatment of primary photoreceptor diseases are clinical stage programs. BlueRock was founded in 2016 as a joint venture of Versant Ventures and Leaps by Bayer. Our culture is defined by the courage to persist regardless of the challenge, the urgency to transform medicine and deliver hope, integrity guided by mission, and community-mindedness with the understanding that we are all part of something bigger than ourselves.

What Are We Doing?

Our foundational science harnesses the ability to create and then direct the differentiation of universal pluripotent stem cells into authentic, functional cells that can be used as allogeneic cellular therapies to treat a broad array of diseases. We can also further engineer these cells, enabling them to produce enzymes, antibodies, and other proteins for additional therapeutic benefit.

We are passionate about delivering on the promise of cellular and gene therapy, shaping the future of cellular medicine, and delivering new therapies to millions of patients with treatment options.

We are seeking individuals who are collaborative, thrive in a fun and dynamic culture, and are steadfast in the commitment to advance cutting-edge cellular therapies to impact patients’ lives.

The Head of Medical Writing will provide strategic and operational leadership for all Medical Writing activities to support BlueRock’s portfolio, from early development through product registration.

This role is accountable for establishing and overseeing a cohesive, scalable Medical Writing function that delivers high-quality regulatory documents that are aligned with BlueRock’s global strategy, development timelines, and corporate priorities. The Head of Medical Writing will develop and lead an internal medical writing team, oversee vendor partnerships, and serve as a key strategic partner to Regulatory Affairs, Pharmacovigilance, Clinical Development, Clinical Operations, Biometrics, Translational Science, and Technical Operations. This role will also help shape future-state capabilities, including AI-enabled medical writing, platform-based content reuse, and collaboration models with Bayer colleagues.

Responsibilities:

Define and own a Medical Writing strategy and roadmap that is aligned with BlueRock’s pipeline, regulatory milestones, and long-term growth.

Establish standards, processes, and governance to ensure consistency, quality, and inspection readiness across all Medical Writing deliverables.

Partner with Regulatory Affairs leadership to ensure that Medical Writing is fully integrated into regulatory strategy, Regulatory Agency engagement, and submission planning.

Drive a platform-based approach to document development, enabling efficiencies and reuse of content across programs where appropriate.

Represent Medical Writing in cross-company forums as needed.

Operational Excellence:

Provide oversight and accountability for all Medical Writing deliverables across BlueRock’s portfolio, including clinical study protocols, IBs, INDs/CTAs, briefing books, Agency responses, DSURs/annual reports, CSRs, integrated summaries, and BLA/MAA modules.

Ensure delivery of documents that are on time, of high quality, and aligned with evolving global regulatory expectations.

Identify opportunities to improve speed, quality, and scalability of document development.

Lead resource planning (internal FTEs and external medical writing vendors) to support current and future program needs.

Oversee and manage vendors and consultants to ensure consistent value, quality, and alignment.

Serve as escalation point for complex document development challenges.

Build, lead, and develop a high-performing internal Medical Writing team, including Associate Directors and/or Principal Medical Writers.

Provide coaching, mentoring, and performance management to support professional growth and retention.

Foster a culture of accountability, collaboration, and continuous improvement

Lead initiatives to modernize Medical Writing activities, including evaluation and pilot implementation of:

AI-enabled authoring, QC reviews, and content reuse tools

Digital workflows and submission efficiencies

Define and manage collaboration models with Bayer, including potential shared services and/or AI-enabled pilots.

Minimum Requirements:

PhD, PharmD, MD, or other advanced degree in a scientific/medical discipline preferred; Bachelor’s degree required.

10+ years of medical writing experience within the biopharma industry; experience with cell and/or gene therapies strongly preferred.

Demonstrated leadership of global regulatory writing programs, including INDs/CTAs and marketing applications (BLAs/MAAs).

Deep understanding of drug and biologics development, CTD structure, ICH and GxP guidelines, regulatory interactions, and submission processes.

Proven leadership, including building and managing teams.

Strong strategic thinking combined with hands-on execution capability.

Excellent written and verbal communication skills.

Experience working cross-functionally in fast-paced, matrixed organizations.

Familiarity with document management systems and authoring tools (eg, Veeva, SharePoint, StartingPoint).

Ability to travel within US/Canada (and limited EU travel, potentially) up to 20%.

Target Base Salary: $198,000 - $233,300

#LI-AL1

BlueRock Therapeutics Company Culture Highlights

Winner of Boston Business Journal's Best Places to Work (Mid-size Company) 2023

Winner of Comparably's Award for Best Company for Diversity 2022

Winner of Comparably's Award for Best Company for Women 2022

Winner of Comparably's Award for Best CEO 2022

BlueRock Therapeutics is ranked in the top 5% of companies for Overall Culture on Comparably.

Engineering Department is ranked in the top 5% of companies for Overall Culture on Comparably.

Check us out on Comparably: https://www.comparably.com/companies/bluerock-therapeutics

Equal Opportunity Workplace:At BlueRock, we welcome and support differences and diversity and we are proud to be an equal opportunity workplace. Please let us know if you require disability-related accommodation or other grounds protected by human rights legislation during the recruitment process so that we can work with you to meet your needs.

Director, Head of Medical Writing

Responsibilities:

Operational Excellence:

Minimum Requirements:

Explore Legal

Skills in this job

People also search for