Reference Number: JO-2109-475857
Senior Director Clinical Development B-Cell
Rate: £250,800 – 266,400
Job Type: Permanent
Location: United States

Senior Director Clinical Development B-Cell Program

World Class Biopharmaceutical Company  

Location: Remote flexibility 

Salary: $320,000 – $340,000 basic salary

Benefits: 25% Bonus, Equity, Medical Benefits & more  


Cpl Physicians are exclusively supporting a clinical stage biopharmaceutical company currently leading the way in oncology development. With over $300M in funding, their novel platform/technology is allowing them to expand into new disease areas at a rapid rate. With a focus across Hematology & Solid Tumors the organization are seeking a Senior Medical Director Clinical Development who ideally has a scientific understanding in the Lymphoma space to work closely with the leadership team to support on two ongoing early phase studies. 


The Senior Medical Director will join the business at a rapid time of growth and will have access to a large number of resources. Working closely with the Vice President Clinical Development this individual will immediately be responsible for the medical monitoring and oversight of 2 studies in the B-Cell program. As the company continues to grow this role allows for a large amount of cross functional exposure to include interactions with regulatory authorities, close partnership with current investigators and input into the wider clinical development plans. This role will come with long term progression allowing you to develop into a more senior role with the business. Ideally individuals will have experience in Lymphoma, but general Oncology/Hematology backgrounds are also of great interest. You will be involved not only in the regulatory discussions but also a high level of contribution to the broader clinical development strategy. 


Responsibilities will include:

• Responsible for the oversight and Medical Monitoring of 2 early phase clinical studies 

• High level of interaction with current investigators with input into regulatory activities 

• Support the Vice President and leadership team with wider clinical development plans and strategies 

• Formulate study designs, lead protocol development, and support cross functional teams in study start-up activities 

• Involved in all aspects of the study conduct with hands-on direct involvement 

• Responsible for playing a key role in Health Authority Interactions reviewing available data that could support future clinical trials 

• Attend and present at investigator meetings and site initiation visits 



• Medical Degree (MD, MBBS, DO)

• Prior industry experience in Clinical Development/Research is preferred 

• Board Certified Physicians in Hematology / Medical Oncology in Academia will be considered

• Medical Monitoring experience 

• Scientific understanding in various Oncology/Hematology disease areas

• Early phase clinical development experience responsible for designing and executing trials 

• Excellent communication skills with a high level of intellectual curiosity 



The successful candidate will receive an executive level basic salary with a benefits package to include the likes of a bonus scheme, stock options, medical benefits and more 


CPL Physicians is a specialist US based retained search and contingent staffing firm focusing exclusively on the recruitment of pharmaceutical physicians for pharmaceutical companies, biotechnology firms, Clinical Research Organisations (CROs) and Regulatory Authorities.

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