About this role.
This Associate Scientific Director role leads evidence-based medical communications programs for pharmaceutical and biotech clients. The position combines advanced scientific writing, strategic content development, quality control, and direct collaboration with clients, authors, and key opinion leaders. It also involves mentoring medical writers, supporting regulatory review and advisory-board activities, and contributing to business growth initiatives. Candidates need an MD, PhD, or PharmD, plus at least 2–3 years of medical communications agency experience. Success requires scientific rigor, polished storytelling, strong stakeholder management, and the ability to manage several fast-moving projects.
Role DNA
A quick view of the complexity, pace, ownership and collaboration implied by the job description.
Job Complexity
4/5Pace & Pressure
4/5Autonomy Level
4/5Communication Load
5/5Salary analysis
Estimated compensation compared with the broader US market for similar roles.
Core skills
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Sample interview questions
I begin by identifying the audience, communication objective, and evidence hierarchy. I extract the most decision-relevant findings, verify every claim against source data, and structure the narrative around a concise scientific takeaway while clearly communicating limitations and clinical context.
I use a structured review process covering scientific accuracy, source verification, consistency of claims, reference integrity, brand and style requirements, and regulatory considerations. I also ensure reviewer feedback is reconciled transparently and that final materials are aligned with the approved strategic brief.
I would clarify the underlying objective and identify where the feedback differs on evidence, strategy, or preference. I would provide an evidence-based recommendation, explain risks or trade-offs, and facilitate a documented decision that preserves scientific integrity and project timelines.
I set clear expectations for the brief, audience, evidence standards, and review milestones, then provide specific, actionable feedback on scientific reasoning and storytelling. My goal is to improve the immediate deliverable while building the writer's confidence and independence for future projects.
I regularly review peer-reviewed literature, congress outputs, clinical-trial updates, treatment guidelines, and competitive activity. I synthesize relevant changes into practical implications for the client's evidence narrative, stakeholder education, and future communication strategy.
Are you passionate about translating cutting-edge science into meaningful outcomes for patients? Join a collaborative, high-performing medical communications team where your scientific expertise directly informs impactful programs for leading pharmaceutical and biotech clients. In this role, you’ll partner across disciplines to shape strategy, elevate scientific storytelling, and contribute to a culture built on excellence, innovation, and long-standing client success. This is an opportunity to grow within a dynamic organization known for its award-winning work, strong client partnerships, and commitment to professional development.
About You:
- You are energized by interpreting complex scientific data and transforming it into clear, compelling communication
- You thrive in a collaborative, cross-functional environment and enjoy partnering with clients, authors, and internal teams
- You bring strong leadership instincts and enjoy mentoring writers while elevating team output
- You are highly detail-oriented with a commitment to scientific accuracy and editorial excellence
- You stay curious—actively following emerging research, competitive landscapes, and therapeutic advancements
- You are confident presenting scientific perspectives to clients, key opinion leaders, and internal stakeholders
About the Role:
As an Associate Scientific Director, you will play a central role in ensuring all deliverables are evidence-based, strategically aligned, and executed with the highest level of quality. You will partner closely with a Scientific Director and Strategic Account Directors to translate client objectives into impactful scientific content and programs. Acting as both a content expert and team leader, you will guide medical writers, oversee the quality-control process, and contribute to strategic planning across projects.
In this role, you will engage directly with clients, authors, and key opinion leaders, helping shape scientific narratives across therapeutic areas. You’ll contribute to content development, regulatory review, and advisory board planning, while also identifying opportunities for innovation and business growth. Your work will directly support the delivery of strategic medical communications solutions that enhance clinical understanding and patient outcomes.
Required Experience:
- Advanced life sciences degree (MD, PhD, or PharmD)
- 2–3+ years of experience within a medical communications agency
- Demonstrated expertise in medical/scientific writing and content development
- Exceptional written and verbal communication skills
- Proven ability to manage multiple projects and timelines in a fast-paced environment
- Experience collaborating with clients, key opinion leaders, and cross-functional teams
Helpful Experience:
- Prior experience mentoring or managing medical writers
- Exposure to regulatory review processes and advisory board development
- Familiarity with competitive intelligence and therapeutic landscape analysis
- Experience supporting new business development or client growth initiatives
Who We Are
Precision AQ – Medical Communications was founded with the simple belief that the scientific story is the foundation of every pharmaceutical brand. Our teams of inquisitive problem solvers and passionate creators dig deep to translate the science behind today’s cutting-edge therapies, then communicate the science clearly and credibly. Our proven track record of long-tenured relationships with major pharmaceutical companies and leading bio-tech firms, and our inclusive, open-minded team culture are industry leading. This passionate work environment, paired with growth opportunity, professional development, compensation, and benefits, are why Precision AQ – Medical Communications was recognized as a Best Place to Work by the Philadelphia Business Journal for the last three years.
Are you ready to join a team committed to providing the best in science and strategy?
Precision is required by law in some states or cities to include a reasonable estimate of the compensation range for this role. This compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Precision, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. This role is also eligible for a discretionary annual bonus, health insurance, retirement savings benefits, life insurance and disability benefits, parental leave, and paid time off for sick leave and vacation, among other benefits.
Reasonable estimate of the current range
$110,000—$140,000 USD
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Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.
If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at myHR@precisionmedicinegrp.com.
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