Director, Clinical Development

PTC Therapeutics, Inc.

. Provide tactical oversight for clinical and medical aspects of all phases of clinical drug development .

Posted 10/6/2026full-timeUnited StatesLead💰 $266,900 - $336,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in clinical drug development, including clinical trial design, regulatory submissions, and adherence to GCP regulations. Capable of managing global clinical programs and collaborating cross-functionally while effectively communicating with stakeholders.

Highest-signal resume keywords

MD DegreeClinical Drug Development ExperienceClinical Trial DesignRegulatory Submissions ExperienceExcellent Communication Skills

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Clinical Development PlansClinical TrialsGCP RegulationsClinical Data InterpretationStudy ProtocolsClinical Study ReportsInvestigator BrochuresCase Report FormsVendor ManagementAnalytical Thinking

Soft Skills

Excellent Problem-Solving SkillsAbility to Influence Without Direct AuthorityAbility to Work Independently and CollaborativelyExcellent Planning and Organization SkillsAbility to Adapt to Changing Priorities

Tools & Technologies

Microsoft Office

Certifications & Qualifications

Board Certification in Medical/Clinical Specialty

Industry Keywords

Pharmaceutical IndustryBiotechnologyGlobal Drug DevelopmentRegulatory ProcessesRare Disease Clinical Development

About the role

Key responsibilities & impact

Provide tactical oversight for clinical and medical aspects of all phases of clinical drug development
Design, develop and execute Clinical Development Plans, clinical trials and protocols in accordance with GCP regulations
Lead and contribute to analysis of study results and assessment of clinical, regulatory and commercial objectives
Document study results
Represent the clinical/medical function in meetings with key opinion leaders, investigators, regulatory authorities, partners, vendors and consultants
Author or review clinical/medical materials for external audiences
Work cross-functionally with internal departments and external resources
Ensure adherence to regulatory requirements and company SOPs
Review and approve study protocols, amendments, manuals, Investigator Brochures, Clinical Study Reports, consent forms, case report forms and other clinical documents
Approve investigator sites and facilitate investigator meetings
Prepare weekly and/or monthly study update reports covering enrollment, adverse events and study progress
Interpret, summarize and document clinical data for regulatory submissions, manuscripts, promotional materials and publications
Approve and monitor clinical study timelines
Contribute to vendor selection and manage relationships with external vendors, partners and investigators
Represent the clinical study team at cross-functional meetings
Participate in clinical review and recommendation of new opportunities such as target selection and clinical due diligence
Provide clinical/medical input to non-clinical and commercial functions
Perform other tasks assigned by management

Requirements

What you’ll need

MD degree
Minimum of 2 years of clinical drug development experience within a pharmaceutical, biotechnology or related environment
Demonstrated experience managing one or more global clinical programs
Knowledge of the pharmaceutical/biotechnology industry, including global drug development and regulatory processes
Knowledge of R&D, key clinical milestones, and factors influencing critical development and decision-making points
Demonstrated expertise in clinical trial design, conduct and interpretation of clinical data
Previous experience with regulatory submissions
Ability to influence without direct authority
Proficiency with Microsoft Office
Excellent verbal and written communication skills
Ability to work independently and collaboratively in a fast-paced, matrixed team environment
Analytical thinking and excellent problem-solving skills
Ability to adapt to changing priorities and deadlines
Excellent planning, organization and time management skills
Ability to support and prioritize multiple projects
Ability to travel domestically and internationally
Board certification or equivalent in a medical/clinical specialty preferred
Experience working in rare/orphan disease clinical development preferred
Up to 25% travel

Benefits

Comp & perks

Short- and long-term incentives
Medical plan
Dental plan
Vision plan
Retirement savings plan
Hybrid work arrangement
Equal opportunity and inclusive workplace