Director of Clinical Science - San Diego CA
Company: Msccn
Location: San Diego
Posted on: April 2, 2026
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Job Description:
Job Description ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our
organization works with partner companies to source qualified
talent for their open roles. The following position is available to
Veterans, Transitioning Military, National Guard and Reserve
Members, Military Spouses, Wounded Warriors, and their Caregivers .
If you have the required skill set, education requirements, and
experience, please click the submit button and follow the next
steps. Unless specifically stated otherwise, this role is "On-Site"
at the location detailed in the job post. The Director of Clinical
Science plays a key role in clinical development of RazyeBio
radiopharmaceuticals for oncology indications. Working in
collaboration with clinical operations, pharmacovigilance and other
functions the position is responsible for various aspects of
ongoing clinical trial program-related activities within the
relevant therapeutic area. These activities include, but are not
limited to, clinical study start-up/execution/close out, data
analysis/reporting, and potentially support of NDA/MAA filings. Job
Responsibilities: Acquires and utilizes knowledge of clinical trial
design to develop or oversee development of specific study concept
synopses and protocols. Participates in protocol review discussions
concerning scientific and procedural aspects of study design. In
collaboration with Medical Writing and Clinical Operations,
prepares study protocols, amendments, specific sections of study
manuals and Investigator meeting materials, and other documents as
needed with appropriate guidance and supervision. Works with
medical writing vendors to coordinate writing and reviewing of
protocols, ICFs, IBs and other clinical trial documents as needed
Contributes to the design, development, and review of CRFs, Data
Management Manuals, and Data Analysis Plans. Reviews ongoing
clinical data and interacts with CROs to ensure data queries are
addressed and data is clean for database locks. Organizes and
oversees Data Review Committee meetings, including preparation of
slides and other review and meeting materials. With MD supervision,
addresses questions regarding scientific and related procedural
issues from Investigators. Participates in Site initiation visits
and study start up activities. Establishes and maintains positive
relationships with clinical trial investigators and site staff.
Contributes to interactions with key thought leaders in gaining
input on protocols and study designs and strategic direction
Contributes to the preparation and/or review of data listings,
summary tables, study results, manuscripts, and scientific
presentations. Assists in the preparation/review of INDs,
regulatory documents, IND annual report/DSURs, Investigator
Brochures, and NDAs/MAAs. Supports priorities within functional
area. Anticipates moderately complex obstacles within a clinical
study and, with guidance, implements solutions. May be asked to
coordinate teams and provide direction. May lead two or more
specific components of departmental strategic initiatives. Able to
enter a new therapeutic area and summarize scientific information
that is available in published literature to integrate into new
study development. Excellent verbal and written communication
skills and interpersonal skills are required to maintain working
relationship with team members to ensure scientific integrity of
clinical studies. May be sought out for advice by others within the
company to help make better decisions and resolve moderately
complex problems. Additional Qualifications/Responsibilities
Education and Experience: Bachelor's degree in Biological Sciences,
healthcare, or a related field, with 8 years of relevant scientific
and/or drug development experience OR an MS degree with 6 years of
relevant scientific and/or drug development experience. Or PharmD
or PhD with 5 years of experience in clinical research or clinical
pharmacology in a biotech/pharmaceutical company, contract research
organization, or academic institution. Demonstrated ability to be a
fast learner. Demonstrated ability to be flexible and adaptable to
change, to move between projects easily and provide
support/expertise where needed. Experienced with Microsoft Office
(Excel, PowerPoint, etc.) as well as job-related programs such as
SpotFire. Knowledge of FDA, EMA and ICH regulations and guidelines.
Ability to effectively collaborate cross-functionally, across all
levels of the organization. Physical demands: While performing the
duties of this job, the employee is regularly required to sit,
reach with hands and arms, and talk or hear. The employee must
occasionally lift and/or move up to 20 pounds. Specific vision
abilities required by this job include close vision and distance
vision. Work Environment: The noise level in the work environment
is usually moderate. If you come across a role that intrigues you
but doesn’t perfectly line up with your resume, we encourage you to
apply anyway. You could be one step away from work that will
transform your life and career. Compensation Overview: San Diego -
RayzeBio - CA: $227,418 - $275,577
Keywords: Msccn, Santa Ana , Director of Clinical Science - San Diego CA, Science, Research & Development , San Diego, California
