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Director Biotech Clinical Research Jobs (NOW HIRING)

NS Pharma Inc

Director, Clinical Research

Paramus, NJ · On-site

$210K - $240K/yr

Bachelor's Degree in sciences or related field with 10 + years of pharmaceuticals/biotech ... clinical/medical research experience with emphasis on Phase II-IV clinical trials. * Experience in ...

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How much do director biotech clinical research jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for director biotech clinical research in the United States is $54.33, according to ZipRecruiter salary data. Most workers in this role earn between $32.45 and $71.63 per hour, depending on experience, location, and employer.

What does a director of biotech clinical research do?

A Director of Biotech Clinical Research oversees the planning, execution, and management of clinical trials for new biotech products and therapies. They ensure studies comply with regulatory requirements and are conducted ethically and efficiently. This role involves managing cross-functional teams, developing clinical strategies, analyzing data, and collaborating with internal and external stakeholders. Their leadership is crucial in advancing innovative treatments from the laboratory to the market.

What are some common challenges faced by a director of biotech clinical research when overseeing multiple clinical trial phases?

Directors of Biotech Clinical Research often encounter challenges in balancing timelines, budgets, and regulatory compliance across several concurrent trials. Coordinating cross-functional teams—including data management, regulatory affairs, and clinical operations—requires strong leadership and communication skills. Additionally, adapting to unexpected scientific or operational hurdles, such as protocol amendments or patient recruitment delays, is a frequent part of the role. Directors must also ensure adherence to Good Clinical Practice (GCP) standards while fostering innovation and maintaining high-quality results.

What are the key skills and qualifications needed to thrive as a director of biotech clinical research, and why are they important?

To thrive as a Director of Biotech Clinical Research, you need a strong background in clinical research, regulatory affairs, and a relevant advanced degree (PhD, MD, or PharmD are common). Familiarity with clinical trial management systems (CTMS), FDA regulations, GCP guidelines, and often certifications like ACRP or SOCRA are highly valued. Exceptional leadership, strategic planning, and cross-functional communication skills set top performers apart in this role. These skills are critical for ensuring compliance, advancing research goals, and leading successful clinical programs in a complex regulatory environment.

What is the difference between Director Biotech Clinical Research vs Clinical Project Manager?

AspectDirector Biotech Clinical ResearchClinical Project Manager
CredentialsAdvanced degrees (PhD, MD, or MS), industry experienceBachelor's or Master's degree, relevant certifications
Work EnvironmentStrategic leadership, overseeing multiple projectsManaging individual clinical trials, coordinating teams
Employer & Industry UsageBiotech companies, pharmaceutical firmsContract research organizations, biotech, pharma
Search & Comparison IntentHigh-level leadership roles, strategic oversightOperational roles, trial management

The main difference is that the Director Biotech Clinical Research focuses on strategic leadership and overseeing multiple clinical research projects, often requiring advanced degrees and extensive experience. In contrast, a Clinical Project Manager handles the day-to-day management of specific clinical trials, coordinating teams and ensuring trial milestones are met. Both roles are essential in the biotech industry but differ in scope and responsibilities.

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Director Biotech Clinical Research jobs near you
Infographic showing various Director Biotech Clinical Research job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 91% In-person, and 9% Remote job distribution, with an average salary of $113,010 per year, or $54.3 per hour.

Clinical Research Site Director

DM Clinical Research

Baltimore, MD

Full-time

Re-posted 9 days ago

Job description

Clinical Research Site Director
DM Clinical Research, the largest privately-owned research management organization in the Houston area and one of the top 50 in the country, is looking for an experienced Clinical Research Site Director to join our team of professionals. This role will be responsible for managing clinical trials from startup to closeout by coordinating site operations.
Responsibilities and Duties:
  • Completing all the DMCR-required training, including but not limited to ICH-GCP Certification and IATA Certification on a timely basis.
  • Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents and assigned study protocol(s).
  • Responsible for immediate supervision and performance of the assigned site staff.
  • Completing all the relevant training prior to study-start and on a continued basis in a timely manner. This will include, but is not limited to:
    • Sponsor provided and IRB approved Protocol Training
    • All relevant Protocol Amendments Training
    • Any study specific Manuals Training as applicable
    • Sponsor-specified EDC and/or IVRS and any other relevant Electronic Systems training.
It is the responsibility of the Site Director to make sure all the relevant training is completed prior to performing any applicable tasks on the assigned study.
  • Working knowledge of the recruitment and relevant cross functional departmental processes for their assigned protocol(s) at their respective site(s).
  • Ensuring visit preparedness for all the relevant sponsor and CRO visits for their assigned protocol(s) and appropriate as well as timely follow up on the action items, at their respective sites.
  • Making sure that the most recent versions of the Protocol, Informed Consents, Study Manuals and all the other relevant study related documents are utilized and implemented at all times for the assigned protocol(s) at their respective site(s).
  • Working with the Regulatory Team to ensure maintenance of Essential Clinical Trial Documents and maintenance of the Investigator Site Binders for their as for their assigned protocol(s) at their respective site(s)
  • Working with the cross functional team(s) and site team(s) to ensure study start readiness on all the aspects and adequate training completed by all the relevant site staff prior to FPFV.
  • Ensuring clinical trial management from FPFV to study close out with strict adherence to study protocol, adherence to all other relevant study manuals, study documents, ICH-GCP Guidelines, FDA Regulations, and ALCOA-C standards, organizational SOPs and guidance documents.
  • Responsible for providing guidance to the site team on planning and monitoring the conduct of the clinical trials.
  • Accomplishing site objectives by managing staff; facilitating staff training as applicable; communicating job expectations
  • Coaching, counseling and disciplining the employees as applicable.
  • Collaborating with both internal and external cross-functional stakeholders for the successful conduct and management of assigned protocol(s) at their respective sites.
  • To develop, coordinate, and enforce site specific systems, policies, procedures, and productivity standards.
  • Communicating and effective implementation of strategic goals from senior management
  • Striving to meet Sponsor subject enrollment goals for their assigned protocols at their respective site(s).
  • Striving to ensure weekly, monthly and quarterly assigned goals are met for their respective site(s).
  • Being prepared for and available at all required company meetings.
  • Submitting required administrative paperwork per company timelines.
  • Occasionally attending out-of-town Investigator Meetings.
  • Any other matters as assigned by management.
Experience and Skill Requirements:
  • Minimum of 8-year experience in Clinical Research.
  • 5 years Experience Managing Multiple Clinical Trials
  • Experience Managing Teams

Apply