Associate Director Clinical Research Science
Associate Director Clinical Research Science
Mural Oncology
Waltham, MA
See who Mural Oncology has hired for this role
Mural Oncology is a clinical-stage oncology business focused on discovering and developing immunotherapies that may meaningfully improve the lives of patients with cancer. By leveraging its core competencies in immune cell modulation and protein engineering, Mural Oncology has developed a portfolio of novel, investigational cytokine therapies designed to address areas of unmet need for patients with a variety of cancers. The Company's lead product candidate, nemvaleukin alfa, is an investigational, engineered interleukin-2 (IL-2) cytokine designed to capture and expand the therapeutic benefits of high-dose recombinant human IL-2, while mitigating its hallmark toxicities.
Associate Director, Clinical Research Science
The Clinical Development Group collaborates closely and maintains excellent working relationships with various internal groups, including but not limited to: Clinical Operations, Biometrics, Data Management, Pharmacovigilance & Drug Safety, Translational Medicine, Preclinical Science, Regulatory Affairs, and Medical Affairs. Clinical programs are developed in conjunction with input from external subject matter experts and consultants and are executed through partnerships with clinical research organizations.
Clinical Development is composed of a "hands-on" group of dedicated professionals. Team members work flexibly and collaboratively together in a matrix environment, with a high degree of personal accountability for the success of novel and aggressive clinical programs and timelines.
Responsibilities
The CRS contributes to five key areas:
Ensures Quality Medical Science
An advanced degree (Ph.D. or Pharm.D.) in a related field A background in life sciences 4+ years of experience working in the pharmaceutical industry Clinical study design, data collection, analysis, and data interpretation skills Experience working in oncology and or immuno-oncology Experience interacting with clinical investigators and medical experts Excellent verbal, written, and interpersonal communication skills (fluency in English is required) Domestic travel (approximately
Preferred Qualifications
Associate Director, Clinical Research Science
The Clinical Development Group collaborates closely and maintains excellent working relationships with various internal groups, including but not limited to: Clinical Operations, Biometrics, Data Management, Pharmacovigilance & Drug Safety, Translational Medicine, Preclinical Science, Regulatory Affairs, and Medical Affairs. Clinical programs are developed in conjunction with input from external subject matter experts and consultants and are executed through partnerships with clinical research organizations.
Clinical Development is composed of a "hands-on" group of dedicated professionals. Team members work flexibly and collaboratively together in a matrix environment, with a high degree of personal accountability for the success of novel and aggressive clinical programs and timelines.
Responsibilities
The CRS contributes to five key areas:
Ensures Quality Medical Science
- Leadership position in developing clinical study protocols, heath authority documents and other study related documents
- Ensures the study team, CRO and clinical trial sites understand and comply with the study protocol
- Serves as the Clinical Scientist on the study team and supports the Medical Monitor in leading review and interpretation of clinical data
- Ensures CRF design supports data collection in alignment with the protocol in collaboration with Data Management
- Collaborates cross-functionally as well as with the CRO to monitor clinical data to ensure quality, completeness, and integrity of trial conduct and patient safety via review of protocol deviations
- Contributes to clinical development plans
- Conducts literature searches for new indications for a given molecule including treatment, epidemiology etc.
- Provides scientific and clinical rationale to health authority communications
- Supports clinical positions in regulatory interactions
- Contributes to scientific publications including posters, abstracts, and manuscripts
- Develops content and presents at Investigator Meetings and provides protocol or other study-related training to CRAs as well as research staff at trial clinical sites
- Communicates and/or collaborates with external experts such as Data Monitoring Committee Members, Trial Steering Committee, Principal Investigators, Key Opinion Leaders, Cooperative Groups, etc.
- Works cross-functionally with other internal groups (eg, Clinical Operations, Biometrics, Data Management, Pharmacovigilance & Drug Safety, Translational Medicine, Preclinical Science, Regulatory Affairs, Medical Affairs, Business Development, and New Product Planning)
Preferred Qualifications
- Direct involvement with human intervention research
- Track record of publications with human experimental research
- Experience with ICH, GCP and relevant regulatory requirements
-
Seniority level
Director -
Employment type
Full-time -
Job function
Research, Analyst, and Information Technology -
Industries
Biotechnology Research
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