Associate Director of Clinical Sciences

Draig Therapeutics; Boston (MA); On-site; USD 150,000 - 190,000; Full time

Benefits offered by this job

Health coverage

401K

Insurance coverage

Generous vacation

Job summary

Draig Therapeutics, a rapidly growing clinical-stage biotech focused on neuropsychiatric therapies, seeks a seasoned Clinical Scientist to drive data integrity and regulatory submissions in psychiatry trials. You will oversee data interpretation, site engagement, and cross-functional collaboration to advance the pipeline.

The role requires a PhD/MD/PharmD or equivalent with 6+ years in biotech/pharma, travel up to 30%, and strong knowledge of GCP and depression assessment scales.

Qualifications

• Advanced degree (PhD, PharmD, MD, or equivalent) required; neuroscience or psychiatry focus strongly preferred.
• At least 6 years’ experience in a Clinical Scientist role in the biotech or pharmaceutical industry; management of people is a plus; for Clinical Scientist, at least two years’ experience in MDD.
• Experience supporting clinical development programs in psychiatry trials.
• Willingness and ability to travel regularly (up to 30%) to clinical sites across the U.S. and Europe.
• Strong understanding of GCP and regulatory requirements.
• Experience interacting with clinical KOLs in psychiatry or CNS.
• Familiarity with depression scales (MADRS, HAM-D, PHQ-9).
• Experience with digital endpoints, ePRO, or decentralized trials is a plus.

Responsibilities

• Review and interpret clinical data on an ongoing basis to ensure data quality and interpretability, and scientific consistency. Participate in the blinded data review (BDA) of the clinical data.
• Conduct regular site visits to engage with investigators and site staff, build relationships, and ensure alignment with protocol objectives and scientific rationale.
• Collaborate closely with clinical operations, medical monitors, data management, biostatistics and other functions throughout the lifecycle of the clinical trial.
• Contribute to the development of study synopsis, study protocols, clinical study reports, INDs, NDAs and their related activities.
• Organize and participate in scientific advisory committees and KOL meetings.
• Support safety surveillance, including review of adverse events and participation in safety review meetings.
• Assist Clinical Operations in study site selection.
• Assist with the development of publications, abstracts, and presentations related to study data.
• Plan for the growth scenario within the functional group and may manage other Clinical Scientists members.

Skills

Clinical data interpretation

KOL engagement

Cross-functional collaboration

Regulatory knowledge

Travel up to 30%

Education

PhD/PharmD/MD or equivalent

Neuroscience/psychiatry focus preferred

6+ years Clinical Scientist experience

Experience in MDD

Tools

GCP knowledge

Job description

Draig Therapeutics is an exciting, rapidly growing clinical-stage biotech backed by a transformative $140 million Series A financing - one of the largest ever in neuropsychiatric drug development. We are pioneering innovative small-molecule therapies aimed at fundamentally transforming the treatment landscape for depression and neurological disorders.

Why Join Draig?

At Draig Therapeutics, you’ll join a science-first, mission-driven biotech that is redefining what a small, agile, and deeply collaborative organization can achieve. Backed by strong investors and propelled by a bold CNS discovery pipeline, Draig brings together world-class scientists, a caring culture, and the energy of a company on an incredible growth trajectory. Here, innovation and speed aren’t just encouraged - they’re expected. This is an environment where your voice matters, your leadership has real impact, and your work directly influences how promising molecules move from concept into the clinic. At Draig, you won’t just contribute to groundbreaking science - you’ll help build a biotech with purpose, speed, and heart. For more info, please visit our website.

Responsibilities:

• Review and interpret clinical data on an ongoing basis to ensure data quality and interpretability, and scientific consistency. Participate in the blinded data review (BDA) of the clinical data.
• Conduct regular site visits to engage with investigators and site staff, build relationships, and ensure alignment with protocol objectives and scientific rationale.
• Collaborate closely with clinical operations, medical monitors, data management, biostatistics and other functions (internal and external) throughout the lifecycle of the clinical trial.
• Contribute to the development of study synopsis, study protocols, clinical study reports, INDs, NDAs and their related activities.
• Organize and participate in scientific advisory committees and KOL meetings.
• Support safety surveillance, including review of adverse events and participation in safety review meetings.
• Assist Clinical Operations in study site selection.
• Assist with the development of publications, abstracts, and presentations related to study data.
• Plan for the growth scenario within the functional group and may manage other Clinical Scientists members.

Education and Experience:

• Advanced degree (PhD, PharmD, MD, or equivalent) in a scientific or clinical discipline required; neuroscience or psychiatry focus strongly preferred.
• At least 6 years’ experience in a Clinical Scientist role in the biotech or pharmaceutical industry. Management of people is a plus. For Clinical Scientist, at least two years’ experience in MDD.
• Experience supporting clinical development programs in psychiatry trials.
• Willingness and ability to travel regularly (up to 30%) and as directed by business needs, to clinical sites across the U.S. and Europe.
• Strong understanding of GCP and regulatory requirements.
• Experience interacting with clinical KOLs in psychiatry or CNS.
• Familiarity with depression scales (e.g., MADRS, HAM-D, PHQ-9).
• Experience with digital endpoints, ePRO, or decentralized trials is a plus.

Preferred Skills:

• Strategic thinker with excellent execution and communication abilities.
• Ability to work cross-functionally and independently in a fast-moving environment.
• Ability to work independently, with minimal supervision.
• Excellent communication, and interpersonal skills.
• Strong problem-solving and decision-making abilities.

What Success Looks Like:

• Flawless Clinical Data Integrity: High-quality, timely ongoing review and interpretation of Phase 2/3 data, ensuring scientific consistency, robust safety surveillance, and successful blinded data reviews (BDR) that keep trials inspection-ready.
• Strong Scientific Stakeholder Engagement: Trusted, high-impact relationships built with trial site investigators, key opinion leaders (KOLs) in psychiatry, and internal cross-functional teams to drive protocol alignment and optimize study execution.
• High-Quality Clinical Deliverables: Timely and precise contribution to critical clinical documents (protocols, investigator brochures, clinical study reports) and regulatory submissions (INDs/NDAs) that directly advance Draig’s neuropsychiatric pipeline.

Adaptability:

Responds resourcefully, flexibly, and positively when faced with new challenges, transitions, and demands. Willingly and effectively deals with the stress and complexities of various situations. Moves forward productively and optimistically under conditions of change and uncertainty.

Collaboration:

Embodies and promotes collaboration and works effectively with others across the organization to achieve goals. Demonstrates proficient cross-company communication, cultural sensitivity, and partnership in interactions with others. Involves others in decisions and plans and credits them for their contributions and accomplishments.

Execution:

Drives execution of strategic and operating plans while maintaining operational effectiveness. Conveys a strong sense of urgency around continuous improvement, achieving high-quality results, and accelerating business performance. Addresses problems directly and drives changes necessary to achieve business objectives.

Relationship Building:

Establishes and maintains strong relationships internally and externally. Respects and relates well to management, colleagues, peers, and direct reports. Champions a culture of respect, diversity, and inclusion that values and respects individuals. Earns the respect of others through principled leadership, sound business ethics, and authenticity.

When You Join Draig Therapeutics, You Will Have:

• Customized and competitive health coverage, including medical, dental, and vision
• US: Healthcare Saving Account for medical and dependent care expenses
• US: Eligible from the first day for 401K
• US & UK: A robust package of Draig-paid insurance coverage, including life insurance, short-term, and long-term disability
• Generous vacation allotment

TO ALL AGENCIES: Please, no phone calls or emails to any employee of Draig about our openings. All resumes submitted by search firms/employment agencies to any employee at Draig Therapeutics via email, the internet, or in any form and/or method will be deemed the sole property of Draig Therapeutics unless Draig engaged such search firms/employment agencies for this position and a valid agreement with Draig is in place. In the event a candidate who was submitted outside of the Draig Tx agency engagement process is hired, no fee or payment of any kind will be paid.

Draig Therapeutics, Inc. is an equal employment opportunity employer. It does not discriminate against any applicant because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, disability, genetic information, veteran status, military status, application for military service, or any other class protected by state or federal law.