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Medical Director Clinical Development Jobs in Florida

Medical Director

Tampa, FL · On-site

$220 - $300/hr

... development, and enhance the patient experience. This role offers the opportunity to balance ... Opportunity to combine clinical practice with medical leadership * Outpatient primary care ...

The Medical Director oversees the activities of group providers, analyzes results and provides ... Collaborates in the development and periodic review of written clinical policies, guidelines and ...

The Medical Director oversees the activities of group providers, analyzes results and provides ... Collaborates in the development and periodic review of written clinical policies, guidelines and ...

Leads various initiatives related to medical care delivery and clinical services, including cost ... Participates in and leads future development initiatives for the organization. * Delivers direct ...

Leads various initiatives related to medical care delivery and clinical services, including cost ... Participates in and leads future development initiatives for the organization. * Provides direct ...

We are seeking a Medical Director to join our team at Independent Living Systems (ILS). ILS, along ... Provide clinical expertise and guidance in the development of health plan policies and programs.

Medical Director

Miami, FL · On-site

$90 - $125/hr

Policy Development: Assist in developing, implementing, and updating clinical protocols. * Provider ... May not serve as the Medical Director for more than five (5) healthcare clinics with a cumulative ...

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Medical Director Clinical Development information

See Florida salary details

$9.7K

$173.6K

$266.8K

How much do medical director clinical development jobs pay per year?

As of Sep 6, 2026, the average yearly pay for medical director clinical development in Florida is $173,647.00, according to ZipRecruiter salary data. Most workers in this role earn between $148,000.00 and $212,600.00 per year, depending on experience, location, and employer.

What does a medical director clinical development do?

A Medical Director of Clinical Development is responsible for overseeing the planning, execution, and management of clinical trials for new drugs or medical products. They work closely with cross-functional teams, such as regulatory affairs, clinical operations, and research scientists, to ensure that clinical studies are designed effectively and conducted in compliance with regulatory standards. Their role also includes reviewing and interpreting clinical data, providing medical expertise, and contributing to the overall strategy for product development. Medical Directors play a crucial role in ensuring the safety and efficacy of new therapies before they reach the market.

How does a medical director clinical development typically collaborate with cross-functional teams during a clinical trial?

As a Medical Director in Clinical Development, you will regularly collaborate with cross-functional teams such as clinical operations, regulatory affairs, biostatistics, data management, and pharmacovigilance. Your role involves providing medical and scientific guidance, ensuring protocol adherence, and addressing safety or efficacy concerns throughout the trial. Effective communication and teamwork are essential for aligning on trial objectives, managing timelines, and resolving any emerging issues. This collaborative environment fosters a comprehensive approach to advancing clinical programs and supports the successful execution of clinical trials.

What are the key skills and qualifications needed to thrive as a medical director clinical development, and why are they important?

To thrive as a Medical Director Clinical Development, you need an advanced medical degree (MD or equivalent), extensive clinical research experience, and a deep understanding of regulatory requirements and drug development processes. Familiarity with electronic data capture systems, clinical trial management software, and GCP/ICH guidelines is typically required. Strong leadership, strategic thinking, and exceptional communication skills help drive multidisciplinary teams and manage complex projects. These skills ensure the safe, efficient, and compliant progression of clinical programs from conception through regulatory approval.

What is the difference between Medical Director Clinical Development vs Medical Scientist?

AspectMedical Director Clinical DevelopmentMedical Scientist
Required CredentialsMD or DO, clinical research experience, industry certificationsMD, PhD, or equivalent, research-focused
Work EnvironmentPharmaceutical companies, biotech firms, clinical trial oversightResearch institutions, academia, laboratories
Employer & Industry UsageCommonly employed in industry to oversee clinical developmentPrimarily in research and academia, less in industry

The Medical Director Clinical Development typically oversees clinical trials and ensures regulatory compliance within the industry, requiring medical credentials and industry experience. Medical Scientists focus on research and discovery, often working in labs or academic settings. While both roles require advanced degrees, their work environments and primary responsibilities differ significantly.

What are popular job titles related to Medical Director Clinical Development jobs in Florida?

For Medical Director Clinical Development jobs in Florida, the most frequently searched job titles are:

What job categories do people searching Medical Director Clinical Development jobs in Florida look for?

The top searched job categories for Medical Director Clinical Development jobs in Florida are:

What cities in Florida are hiring for Medical Director Clinical Development jobs?

Cities in Florida with the most Medical Director Clinical Development job openings:

Infographic showing various Medical Director Clinical Development job openings in Florida as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $173,647 per year, or $83.5 per hour.

Clinical Development Medical Director, Hematology

Pfizer

Tampa, FL • On-site

$240 - $400/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 8 days ago


Key responsibilities

  • Oversee the design, conduct, and analysis of late-phase clinical trials in Hematology.

  • Provide medical monitoring activities including eligibility assessment, data review, and safety monitoring.

  • Collaborate with cross-functional teams to review and interpret clinical data, and communicate findings to stakeholders.


Pfizer rating

8.2

Company rating: 8.2 out of 10

Based on 126 frontline employees who took The Breakroom Quiz

33rd of 86 rated pharmaceutical


Job description

Clinical Development Medical Director, Hematology page is loaded## Clinical Development Medical Director, Hematologytime type: 全职posted on: 发布于昨天job requisition id: 4961307**Job Summary**The medical director provides Clinical Development leadership and expertise on Late phase clinical trials, including overseeing the design, conduct, and analysis within Hematology. The medical director works closely with other functions such as regulatory affairs, pharmacovigilance, biostatistics, and medical affairs to ensure that the clinical development program meets the scientific, ethical, and regulatory standards. The medical director also provides medical expertise and guidance to the clinical operations team, the investigators, and the external stakeholders such as health authorities, ethics committees, and patient advocacy groups.**Job Responsibilities***Study-level Clinical Development Leadership*· Collaborate with Clinical Scientist(s) to provide clinical leadership across 2-3 study team(s) that is scientifically rigorous and aligns with company objectives.· Conduct medical monitoring activities including eligibility assessment, data review and safety monitoring.· Lead peer-to-peer interactions with investigators.· Serve as the point of contact for clinical issues between the study team, investigators, ethics committees, steering committees, and regulatory authorities.· Lead and contribute to development and maintenance of clinical trial and regulatory documents, in collaboration with Clinical Scientist and the cross-functional team.*Strategic Guidance, Clinical Insights & Interpretation*· Collaborate with Clinical Scientist to review and interpret clinical data, identify key findings and implications, and communicate to internal and external stakeholders.· Maintains a high level of clinical expertise and professional competence by staying abreast of the latest developments, literature, and guidelines to advise on and drive current and future clinical development plans.**Basic Qualifications*** Clinical Development experience required* Medical Degree with 4+ years experience* As medically qualified individual, the successful candidate must have the following qualifications:+ Obtained a primary medical degree (e.g., MD, DO, MBBS, MBChB) from a recognized medical school/university.+ Been licensed by a licensing body/health authority to prescribe medicines independent of Supervision for at least 2 years post their intern/house officer/foundation period.**Preferred Qualifications*** Late-stage clinical development experience preferred* Hematology experience preferred* Board certified/eligible in oncology or equivalent preferred**Organizational Relationships**Reports to Global Development Lead or Senior/Executive Medical DirectorPartners closely subject matter experts within cross-functional study team, Pfizer Oncology Division and counterparts in other divisions within Pfizer.Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.**NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS**Ability to travel to conferences and for team meetings ~4 times per yearRelocation assistance may be available**Work Location Assignment:** **This is a hybrid role requiring you to live within commuting distance and work on-site an average of 2.5 days per week**The annual base salary for this position ranges from $239,900.00 to $399,800.00. In addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 25.0% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life's moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site - U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.This role is posted in multiple locations. If you are applying for the role in an secondary job posting location where pay transparency regulations apply, your Talent Advisor will share the local pay information with you during the first interview.Relocation assistance may be available based on business needs and/or eligibility.Candidates must be authorized to be employed in the U.S. by any employer.U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.**Sunshine Act**Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider's name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.**EEO & Employment Eligibility**Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.Pfizer endeavors to make accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email disabilityrecruitment@pfizer.com. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on .Medical #J-18808-Ljbffr

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About Pfizer

Sourced by ZipRecruiter

All over the world, Pfizer colleagues work together to positively impact health for everyone, everywhere. Our colleagues have the opportunity to grow and develop a career that offers both individual and company success; be part of an ownership culture that values diversity and where all colleagues are energized and engaged; and the ability to impact the health and lives of millions of people. Pfizer, a global leader in the biopharmaceutical industry, is continuously seeking top talent who are inspired by our purpose to innovate to bring therapies to patients that significantly improve their lives. Our Health and Science System Specialists Team provides leadership across patient care settings in the complex Hospital, Health System, and Key Medical Group environment to bring value to our customers and patients in this dynamic ecosystem.

Industry

Pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

New York, NY, US

Year founded

1849