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Cns Trials Jobs (NOW HIRING)

IQVIA

Senior Clinical Lead- CNS

Durham, NC · On-site

Experience managing Clinical Trials as a Global Lead, overseeing sites and CRAs on international trials (includes any of the following regions: NA/EUR/LatAM/APAC) * Experience in CNS .... this is the ...

IQVIA

Senior Clinical Lead- CNS

Durham, NC

Experience managing Clinical Trials as a Global Lead, overseeing sites and CRAs on international trials (includes any of the following regions: NA/EUR/LatAM/APAC) * Experience in CNS .... this is the ...

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How much do cns trials jobs pay per year?

As of Jun 8, 2026, the average yearly pay for cns trials in the United States is $127,453.00, according to ZipRecruiter salary data. Most workers in this role earn between $65,500.00 and $202,000.00 per year, depending on experience, location, and employer.

What are some common challenges faced by professionals working in CNS clinical trials, and how can they be addressed?

Professionals involved in CNS (central nervous system) clinical trials often face unique challenges such as patient recruitment and retention, as neurological disorders can affect participants' ability to consent and adhere to protocols. Additionally, measuring outcomes objectively is complex due to the variability of CNS disorders. These challenges can be addressed by designing patient-centric studies, using clear communication strategies, and leveraging technologies like electronic patient-reported outcomes and wearable devices to gather more reliable data. Collaborating closely with multidisciplinary teams, including neurologists, psychologists, and data managers, is also key to successful trial execution.

What is the difference between Cns Trials vs Clinical Research Coordinator?

AspectCns TrialsClinical Research Coordinator
Required CredentialsTypically requires clinical trial experience, healthcare background, and sometimes certifications like CCRPUsually requires a bachelor's degree in health or related field; certifications like CCRP are common but not mandatory
Work EnvironmentConducts or oversees clinical trials, often in hospitals, research centers, or pharmaceutical companiesManages daily activities of clinical studies at research sites, hospitals, or clinics
Employer & Industry UsageUsed mainly in pharmaceutical, biotech, and clinical research organizationsCommonly employed in hospitals, research institutions, and clinical trial sites

While both roles are involved in clinical research, Cns Trials typically focus on overseeing or conducting clinical trials, requiring specialized experience and certifications. Clinical Research Coordinators handle the day-to-day management of studies, often with less specialized credentials. Understanding these differences helps in choosing the right career path or job search focus.

What are CNS Trials?

CNS Trials refer to clinical studies that investigate treatments, drugs, or interventions targeting the central nervous system (CNS), which includes the brain and spinal cord. These trials are essential for developing therapies for neurological and psychiatric conditions such as Alzheimer's disease, Parkinson's disease, multiple sclerosis, depression, and schizophrenia. CNS trials typically involve multiple phases to ensure the safety and efficacy of new treatments before they become widely available. The complexity of the CNS and the conditions it affects means these trials often require rigorous protocols and specialized expertise.

What are the key skills and qualifications needed to thrive in CNS Clinical Trials, and why are they important?

To thrive in CNS Clinical Trials, you need a solid background in neuroscience, clinical research methodologies, and a relevant science degree, often supplemented by certifications such as GCP (Good Clinical Practice). Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and regulatory documentation is typical. Strong attention to detail, effective communication, and problem-solving abilities help professionals navigate complex studies and work with interdisciplinary teams. These skills and qualifications are crucial for ensuring the integrity, compliance, and successful execution of CNS clinical research.
Infographic showing various Cns Trials job openings in the United States as of May 2026, with employment types broken down into 91% Full Time, 8% Part Time, and 1% Contract. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution, with an average salary of $127,453 per year, or $61.3 per hour.
Medical Director, Clinical Development - CNS

Medical Director, Clinical Development - CNS

Sk Life Science, Inc.

Paramus, NJ • On-site

Full-time

Posted 13 days ago

Job description

Overview
The Director of Clinical Development CNS will be involved in multiple product development projects at SK Life Science (SKLSI). He-she will provide therapeutic and pharmacovigilance expertise to the clinical development of the SKLSI pipeline of therapeutic drugs with particular focus on epilepsy. He/she will also provide clinical operational support to each product development projects. The Director will work with regulatory, discovery, business development, legal, quality and CMC to facilitate the development of SK Life Sciences products. The position will report to the Chief Medical Officer of SK Life Science.
Responsibilities
General
  • Training in Good Clinical Practices (GCP)
  • Knowledge of relevant regulatory guidance for the clinical development process
  • Experience with FDA preferred
  • Reports to Chief Medical Officer

Skills
  • Evidence of ability to work with opinion leaders, principal investigators
  • Must be able to work effectively in a team setting
  • Communication skills necessary to:
    • Represent the Company externally in scientific presentations, conferences and industry groups;
    • Present to internal stakeholders
    • Interact with industry

Responsibilities:
  • Participate in the development of product clinical development plans and clinical trial strategy
  • Participate in the design and conduct of clinical trials and as a member of the Clinical Development team provide operational oversight by collaborating with internal and external clinical operations personnel
  • Provide medical expertise regarding product development or other scientific issues for drug discovery and development
  • Provide medical monitoring directly or oversee medical monitoring by vendors during the conduct of clinical trials
  • Participate in pharmacovigilance activities including SAE evaluation and reporting and analysis of safety data
  • Participate in preparation of documents including but not limited to: protocols, Investigator Brochures, clinical study reports, safety reports, and the clinical sections of Annual Reports, INDs/IMPDs, NDAs/MAAs, SOPs, pediatric investigation plans, as well as abstracts and manuscripts
  • Interface with regulatory agencies for clinical development programs, regulatory submissions, and GCP inspections when necessary
  • Oversee the scientific interaction with relevant medical consultants/advisors and investigators

Qualifications
  • M.D. degree
  • Practice experience preferable but not required
  • Minimum of 3 years of experience in clinical development in the pharmaceutical industry, preferably with neurology compounds or relevant academic research experience
  • Ability to multitask
  • Adapts to change
  • Maintain composure under pressure
  • Ability to follow verbal or written instructions and use of effective verbal communications
  • Adapts change, adjust change and grasps information quickly
  • Examine and observe details
  • Self starter and decision maker
  • 10-20% travel

Apply