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Clinical Development Jobs in New York (NOW HIRING)

Novartis

Clinical Development Medical Director

East Hanover, NJ · On-site +1

$85K - $115K/yr

As the Clinical Development Medical Director (CDMD) in RTL, you will lead the planning and management of the assigned clinical program(s) from an end-to-end clinical development perspective and drive ...

Kite Pharma

Clinical Development Scientist

Parsippany, NJ · On-site

$133K - $172K/yr

You will play a supportive role in late stage oncology clinical development. Working in collaboration with the Clinical Scientist Lead, you are accountable for various aspects of ongoing clinical ...

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Clinical Development information

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$15

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$98

How much do clinical development jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for clinical development in New York is $37.87, according to ZipRecruiter salary data. Most workers in this role earn between $18.12 and $36.01 per hour, depending on experience, location, and employer.

What is the difference between Clinical Development vs Clinical Research Coordinator?

AspectClinical DevelopmentClinical Research Coordinator
Required CredentialsBachelor's degree, often advanced degrees in life sciences or related fields; certifications like CCRP or RACBachelor's degree in health sciences or related field; certifications like CCRP beneficial
Work EnvironmentPharmaceutical or biotech companies, clinical trial teams, R&D departmentsClinical trial sites, hospitals, research centers
Employer & Industry UsageUsed in pharmaceutical, biotech, and medical device industries during drug development phasesUsed in hospitals, research institutions, and clinical trial sites for managing patient studies

While both roles are involved in clinical trials, Clinical Development focuses on designing and managing the overall drug development process, whereas Clinical Research Coordinators handle the day-to-day operations at trial sites, ensuring protocol adherence and patient coordination.

What is clinical development?

Clinical development is the process by which new pharmaceutical drugs, biologics, or medical devices are tested and evaluated in humans to assess their safety and effectiveness. It typically involves a series of phases (Phase I-IV) of clinical trials, starting with small groups of volunteers and expanding to larger patient populations. The goal is to gather the data needed for regulatory approval and to ensure that new treatments provide benefits that outweigh their risks. Clinical development is a critical step in bringing new therapies from the laboratory to patients.

What do you do in clinical development?

A professional in clinical development designs, manages, and oversees clinical trials to evaluate the safety and effectiveness of new medical treatments or drugs. They coordinate with cross-functional teams, ensure compliance with regulatory standards, and analyze data to support product approval processes. Strong project management skills and knowledge of Good Clinical Practice (GCP) are essential in this role.

What does a clinical development specialist do?

A clinical development specialist designs, manages, and oversees clinical trials to evaluate the safety and effectiveness of new medical treatments or devices. They coordinate with research teams, ensure compliance with regulatory requirements, and analyze data to support product approval processes. Strong knowledge of Good Clinical Practice (GCP) and clinical trial management systems is essential for this role.

What are the key skills and qualifications needed to thrive in clinical development?

To thrive in Clinical Development, you need a strong background in life sciences, clinical trial management, and regulatory compliance, often supported by a relevant degree and experience in clinical research. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications like GCP (Good Clinical Practice) are typically required. Excellent communication, problem-solving, and leadership skills help professionals coordinate multidisciplinary teams and adapt to evolving study demands. These skills and qualifications ensure the design, execution, and oversight of safe, effective, and compliant clinical trials essential for successful drug development.

What are some common challenges faced in a clinical development role, and how can I prepare for them?

Professionals in Clinical Development often encounter challenges such as managing complex regulatory requirements, coordinating multi-site clinical trials, and ensuring timely patient recruitment. Staying organized, maintaining clear communication with cross-functional teams, and keeping up-to-date with evolving industry guidelines can help you navigate these hurdles. Developing strong project management and problem-solving skills is also essential for success in this dynamic field.
What are the most commonly searched types of Clinical Development jobs in New York? The most popular types of Clinical Development jobs in New York are:
What are popular job titles related to Clinical Development jobs in New York? For Clinical Development jobs in New York, the most frequently searched job titles are:
What job categories do people searching Clinical Development jobs in New York look for? The top searched job categories for Clinical Development jobs in New York are:
What cities in New York are hiring for Clinical Development jobs? Cities in New York with the most Clinical Development job openings:
Clinical Development jobs near you
Infographic showing various Clinical Development job openings in New York as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 15% Part Time, and 3% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $78,773 per year, or $37.9 per hour.

Senior Director, Clinical Development

Mallinckrodt

Bridgewater, NJ • On-site

$81K - $111K/yr

Full-time

Re-posted 11 days ago

Mallinckrodt rating

8.0

Company rating: 8.0 out of 10

Based on 11 frontline employees who took The Breakroom Quiz

43rd of 86 rated pharmaceutical

Job description

Job Title
Senior Director, Clinical Development
Requisition
JR000015848 Senior Director, Clinical Development (Open)
Location
Bridgewater, NJ
Additional Locations
Malvern, PA, Philadelphia, PA
Job Description Summary
Job Description
The Senior Director, Clinical Development (CD) is responsible for providing expert clinical advice across all phases (phase II-IV) of clinical research and will be the responsible clinical lead from the Clinical Development function. They will be responsible for oversight and management of the clinical development execution aspects of clinical development programs. Generally, the role will oversee multiple clinical study programs and/or therapeutic focus areas and establish a resource model to support those activities with both external and internal resources when / as indicated. This role has the ultimate oversight responsibility for leading CD activities including the design and development of clinical studies, writing in collaboration with Medical Writing, the required clinical documents such as, but not limited to, protocol concept form, clinical study synopsis, clinical study protocol, investigator brochures etc. They are ultimately accountable for the on-time achievement of study and/or program milestones in alignment with the program team strategic imperatives.
This position is also the clinical point of contact between internal teams and external groups such as clinical operations, vendors (CROs, central laboratories, etc.), investigators, regulatory authorities, medical affairs, Key Opinion Leaders, Advisory Boards, etc.
Key Accountabilities
Clinical Lead
  • Acts as the lead clinical representative on Project Teams.
  • Act as the key contributor in development of clinical development strategy across multiple indications.
  • Develop, review, guide and approve protocols, and amendments, ICFs, and clinical sections of other documents.
  • Oversee safety monitoring of ongoing clinical studies under their leadership with appropriate support as needed.
  • Interact and lead engagements with thought leaders within the respective therapeutic area/indication.
  • Track with Program Management the CD deliverables across all clinical studies/projects.
  • Lead identifying, contracting and engaging subject matter experts/thought leaders in advisory board meetings, consultancy etc.
  • Oversee regular maintenance and update of the CD project folders/drives.
  • Reviews the informed consent form (ICF); ensures alignment with the related safety sections of the study protocol.
  • Develops, reviews and/or approves clinical and safety and monitoring CRF pages.
  • Act as the key contributor in development of clinical development strategy across multiple indications.
  • Collaborates in study team meetings, data monitoring committee and steering committees as necessary.
  • Helps to identify additional opportunities within the broad R&D portfolio; propose indications and study design approaches for establishing proof of concept and help to identify and evaluate opportunities for in-licensing or mergers/acquisitions that would expand the platform portfolio.

Clinical Study Planning Development, Data and Reports
  • Review, guide and finalize study documents such as Protocol Synopses, Protocols, Protocol amendments, Administrative Change letters etc.
  • Ensure CD contributions to trial-related documents such as the IBs, ICF, CRFs, CRF Completion Guidelines, Study Execution and Monitoring Plans, Clinical Data Review Plan, Clinical Database specifications, statistical analysis plan, the data management plan, the safety management plan, the medical monitoring plan, Clinical Study Report (CSR) etc.
  • Ensure regular and ad-hoc data reviews and interpretation; preparation of summaries/documentations of these reviews to Leadership.
  • Ensure timely development of program-level documents, including, but not limited to, abstract and manuscripts, presentations, and various other internal and external documents and communications as needed.
  • Work collaboratively with the clinical study team and other team members to prepare abstracts, manuscripts and presentations for external meetings as well as author clinical sections of regulatory documents (CSRs, IBs, IND sections, CTAs, ISS and ISE sections and clinical expert reports).

Clinical Operations
  • In collaboration with the Development Operations staff, develops the operational strategies for clinical research studies and development programs including, but not limited to, PI selection, CRO selection, budgets, and timelines.
  • Ensure CD participation in vendor selection, specification development, and management/oversight, as needed.
  • Ensure development of study specific training materials for study team, investigational sites, and vendors.
  • Participate and present at Investigator meetings or similar.
  • Lead the responses to scientific and data-related queries.
  • Collaborate with statistician in data review and interpretations.

Safety & Efficacy
  • Act as the primary medical monitor with support as required to identify any trial-related safety trends, and as needed, generate reports to interpret, analyze and summarize the data and trends.
  • Develop and/or review narratives for AEs/SAEs/AESIs as necessary.
  • Collaborate with the statistician to identify any trial-related efficacy trends, and as needed, generate reports to interpret, analyze and summarize the data and trends.

Qualifications
Education & Experience
  • Board licensed MD (or equivalent foreign qualification) in Immunology
  • Minimum of 8-10 years of Clinical Development experience (pharma, CRO) in Immunology/Autoimmunity
  • Previous experience designing and developing phase 1-4 protocols.
  • Therapeutic area experience preferred (demonstrable with 2 or more years relevant experience).
  • Demonstrates ability to analyze and interpret data, assess clinical relevance and present/report findings (e.g., ISS, ISE, competitor data, etc.).
  • Experience working on a matrix cross-functional clinical team.
  • Previous project management/clinical operations experience desirable.

Knowledge
  • Demonstrated ability to manage multiple and diverse projects concurrently.
  • Demonstrated ability to develop relationships and generate collaborations.
  • Strong analytical skills; a strategic thinker, planner and implementer; proven negotiating track record.
  • Solid Medical/Scientific writing skills required with appropriate clinical, scientific and medical knowledge to author and design and implement clinical protocol and other study documents.
  • Working knowledge of statistics, data analysis and data interpretation.
  • Experience with the operation aspects of clinical trials and related activities such as investigator meetings, DSMB's and GCP/ICH are necessary.
  • Excellent written and oral communication skills.
  • Organizational and cross functional collaboration skills.
  • Proficient in Microsoft Office Suite of Programs

Skills & Abilities
  • Strong interpersonal and communication skills (verbal and written) bridging scientific and business needs, integrating clinical science, disease area knowledge, and operational requirements.
  • Incumbent must be able to work with colleagues at all levels of responsibility and authority.
  • Ability to work on multiple projects with aggressive timelines
  • Action oriented, flexible, able to adapt to changes in priorities, projects, and daily activities.
  • Strong presentation skills
  • Strong MSP skills

Physical Requirements
  • Up to 20% travel

Keenova offers employees a Total Rewards package which includes competitive pay and benefits. To learn more about our Total Rewards benefits please visit: Keenova Careers | Serve and Grow with Purpose | Keenova
The expected base pay range for this position is $285K - $315K. Please note that base pay offered may vary depending on factors including job-related knowledge, skills, and experience.
This position is eligible for a bonus in accordance with the terms of the applicable program. Bonuses are awarded at the Company's discretion.
Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.
#LI-HYBRID
#LI-JP1
At Keenova, we believe that no one should be alone in their pursuit of better health. This purpose drives us as we pair quality therapeutics with human support-showing up in big moments and small to help patients find comfort and confidence.
We bring deep expertise and resolve to every therapeutic area we serve, including immunology, urology, men's health, orthopedics, critical care, and pediatric endocrinology. We work with patients, care partners, and physicians to help them navigate healthcare system complexity and access therapies that make a meaningful difference.
We are Keenova-keen to solve, keen to serve. Learn more at www.keenova.com.

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