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Volunteer Director Bioanalytical information

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$29.5K

$76.9K

$119.5K

How much do volunteer director bioanalytical jobs pay per year?

As of Aug 8, 2026, the average yearly pay for volunteer director bioanalytical in the United States is $76,855.00, according to ZipRecruiter salary data. Most workers in this role earn between $56,500.00 and $90,000.00 per year, depending on experience, location, and employer.

What does a volunteer director bioanalytical do?

A Volunteer Director Bioanalytical oversees and coordinates volunteer-based bioanalytical projects or teams, often within research organizations, non-profits, or academic institutions. They are responsible for recruiting, training, and managing volunteers who assist in bioanalytical tasks such as sample collection, data analysis, and laboratory work. Additionally, they ensure compliance with safety and quality standards while facilitating communication between volunteers and scientific staff. Their work supports the efficient and ethical conduct of bioanalytical studies, often contributing to research in fields like public health, pharmaceuticals, or environmental science.

What are some common challenges faced by a volunteer director bioanalytical and how can they be addressed?

A Volunteer Director in a bioanalytical environment often encounters challenges such as coordinating diverse volunteer skill sets, ensuring compliance with laboratory safety standards, and maintaining clear communication between scientists and non-technical volunteers. To address these, it's important to provide thorough orientation and ongoing training tailored to each volunteer's background, establish clear protocols for lab work, and foster an inclusive team atmosphere where questions are encouraged. Regular check-ins and collaborative planning sessions also help streamline workflow and keep everyone aligned on project goals.

What is the difference between Volunteer Director Bioanalytical vs Volunteer Laboratory Supervisor?

AspectVolunteer Director BioanalyticalVolunteer Laboratory Supervisor
Required CredentialsRelevant scientific knowledge, possibly certifications in bioanalysis or related fieldsLaboratory management experience, possibly certifications in lab safety or supervision
Work EnvironmentResearch labs, clinical trial settings, nonprofit research organizationsLaboratories, research facilities, healthcare settings
Employer & Industry UsagePharmaceutical, biotech, research nonprofitsResearch institutions, healthcare providers, nonprofit labs
Common Search & Comparison IntentUnderstanding roles in bioanalytical research and volunteer managementComparing lab supervision roles in volunteer or nonprofit settings

The Volunteer Director Bioanalytical focuses on overseeing bioanalytical research projects and managing volunteer teams in scientific settings. In contrast, the Volunteer Laboratory Supervisor typically manages laboratory operations and staff in research or healthcare labs. Both roles require scientific knowledge and experience working in lab environments, but their responsibilities differ in scope and focus.

What are the key skills and qualifications needed to thrive as a volunteer director bioanalytical?

To excel as a Volunteer Director Bioanalytical, you need a solid background in bioanalytical science, project management experience, and often an advanced degree in a life science field. Familiarity with laboratory information management systems (LIMS), regulatory compliance (such as GLP/GCP), and analytical instrumentation is typically required. Exceptional leadership, communication, and organizational skills help coordinate volunteer teams and ensure project objectives are met. These competencies are crucial for maintaining scientific rigor, regulatory adherence, and effective management of volunteer-driven bioanalytical projects.
More about Volunteer Director Bioanalytical jobs
What cities are hiring for Volunteer Director Bioanalytical jobs? Cities with the most Volunteer Director Bioanalytical job openings:
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Volunteer Director Bioanalytical jobs near you
Infographic showing various Volunteer Director Bioanalytical job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 13% Part Time, 1% Temporary, and 1% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $76,855 per year, or $36.9 per hour.

Sr. Director, Clinical Science (Autoimmune)

Xencor

San Diego, CA • On-site

$84K - $115K/yr

Full-time

Medical, Retirement

Re-posted 22 days ago

Job description

Introduction:
Xencor is a public, clinical-stage biopharmaceutical company located in the Los Angeles area (Pasadena) and in San Diego. Our focus is developing high-potential XmAb® bispecific T-cell engagers and additional engineered drug candidates that leverage our differentiated technology platforms, and we are advancing our pipeline toward clinical proof-of-concept decisions. Our goal is to create high-impact therapeutics for patients with cancer and other serious diseases. More than 20 XmAb drug candidates engineered with our technology are in clinical development, and three XmAb medicines have been marketed by partners. For more information, please visit www.xencor.com. We have an excellent opportunity for a Sr. Director, Clinical Science (Autoimmune), to join our team.
This is a hybrid or remote position. Hybrid would be based out of our San Diego or Pasadena, CA locations.
Summary:
Responsible for facilitating successful and timely initiation and completion of the Company's clinical development programs in Inflammatory Bowel Disease (IBD) and other autoimmune programs by executing and monitoring medical aspects of selected global clinical trials. This role will support the design, execution, monitoring, and interpretation of randomized, placebo-controlled clinical trials in IBD as well as studies in healthy volunteers.
Primary Responsibilities:
  • Creates required clinical trial documents including clinical protocols, investigator brochures, DSURs and clinical modules of the IND (in concert with Study Medical Directors)
  • Works closely with Clinical Operations to execute the clinical trial with high quality and according to timelines
  • Performs ongoing review of clinical data, query generation/resolution and data analysis, including review of draft listings to support data cleaning and interpretation
  • Provides scientific expertise to Clinical Operations by responding to questions and/or by clarifying issues arising during study conduct
  • Provides internal safety monitoring for clinical trials in collaboration with the Study Medical Director
  • Provides medical input for the clinical database build, CRFs, monitoring plan, data management plan, safety monitoring plan and statistical analysis plan
  • Develops and maintains relationships with clinical trial investigators and therapeutic area key opinion leaders
  • Leads review of study data (e.g., tables, listings and figures and emerging bioanalytical data) and develops CSRs, clinical presentations and publications
  • Supports other members of Clinical Development and Regulatory Affairs departments as required
  • Participates as a standing member of multidiscipline Project Teams
  • Adheres to all department and company-wide policies regarding conduct, performance and procedures
  • Provides oversight and direction to direct and indirect reports, as applicable, in accordance with the organization's policies and procedures. The responsibilities may include, but are not limited to recruiting, training, communicating job expectations, appraising and managing job performance, delivering feedback and coaching, and providing career development planning and opportunities
  • Performs other duties as required.

Education/Experience/Skills:
Position requires a BS degree in life sciences; PhD, RN, PharmD or MS preferred and a minimum of 15 years of directly relevant pharmaceutical industry experience in clinical development and a minimum of 4 years' experience of focus in assigned therapeutic area. Experience as a clinical scientist responsible for data review, safety monitoring, protocol development, supporting data analyses, interpretation and publications also required, as well as clinical research experience in IBD on randomized, placebo-controlled trials. Prior experience with translational medicine/early phase clinical trials, monoclonal antibody biologics/immunotherapy, and relevant tasks throughout the entire study life cycle, from study concept to database lock and CSR is preferred.
Position also requires:
  • Strong initiative, motivation, organization and hands on approach with outstanding attention-to-detail
  • Expertise in analysis and interpretation of emerging clinical data, including use of software packages to analyze data (e.g., pivot tables) and EDC: MS Office Suite, Visio, GraphPad Prism, Spotfire, Medidata RAVE, Inform etc.
  • Ability to work independently and prioritize multiple tasks and goals to ensure timely, on-target and within-budget accomplishments
  • Excellent written and oral communication skills and interpersonal skills
  • Ability to adjust style/contents to suit the audience/purpose
  • Self-starter, highly motived, highly organized and hands on with outstanding attention-to-detail
  • Ability to demonstrate competencies applicable for job based on Xencor's Leadership Competency Model
  • Ability to lead cross-functional teams

Occasional travel may be required, including travel between Xencor's Pasadena and San Diego offices. Work for this position is generally performed at Xencor's worksite and requires full-time commitment.
Expected Base Salary Range: $247,700 - $309,000
The actual salary will be based on the selected candidate's qualifications, including skills, competencies, education and experience. Xencor offers a competitive total rewards package including 401k match, healthcare coverage, ESPP and a broad range of other benefits. In addition, this position will be eligible for an annual bonus and equity grant. For more information, please see https://xencor.com/careers/.
Americans with Disabilities Act (ADA) Statement
The Company will provide reasonable accommodations (such as a qualified sign language interpreter or other personal assistance) with the application process upon your request as required to comply with applicable laws. If you have a disability and require assistance in this application process, please contact HR@xencor.com.
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Reasonable Accommodations may be made to enable qualified individuals with disabilities to perform the essential functions.
Equal Employment Opportunity (EEO) Statement
The Company is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, sexual orientation, gender or gender identity, national origin, disability status, protected veteran status or any other characteristic protected by state or federal law.
Xencor does not accept profiles or resumes from recruiting vendors without a binding written agreement. Any unsolicited submission of services and or resumes in no way creates an obligation or duty by Xencor, implied or otherwise.
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About Xencor

Sourced by ZipRecruiter

Industry

Biotechnology research and development

Company size

201 - 500 Employees

Headquarters location

Pasadena, CA, US

Year founded

1997

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