218 Medical Researchers jobs in Los Angeles

Our client, a renowned pharmaceutical innovator based in **Los Angeles, California, US**, is seeking an exceptional Lead Clinical Research Scientist to spearhead critical research initiatives. In this role, you will be at the forefront of designing and executing clinical trials, contributing significantly to the development of novel therapeutics. You will lead a team of dedicated research professionals, providing scientific guidance and strategic direction from study inception through to regulatory submission. This position demands a deep understanding of pharmaceutical R&D processes, regulatory affairs (FDA, EMA), and advanced statistical methodologies. You will be responsible for protocol development, data analysis, interpretation of results, and the preparation of comprehensive scientific reports and publications. The ideal candidate possesses a strong track record in clinical development, particularly in areas such as oncology, immunology, or rare diseases. Your expertise will be vital in identifying target patient populations, designing effective trial endpoints, and ensuring the ethical and scientific integrity of all research activities. You will collaborate closely with internal departments, including preclinical development, regulatory affairs, and medical affairs, as well as external partners such as principal investigators, clinical sites, and contract research organizations (CROs). A Master's or Ph.D. in a relevant scientific discipline (e.g., Pharmacology, Biochemistry, Biomedical Sciences) is required, coupled with substantial experience in clinical trial management and data interpretation. This role requires exceptional leadership qualities, strong analytical and critical thinking skills, and the ability to effectively communicate complex scientific information to diverse audiences. You will contribute to the strategic planning of the company's R&D pipeline, ensuring that clinical development programs are robust, efficient, and aligned with global regulatory requirements. We are looking for a proactive, results-oriented individual who can thrive in a fast-paced, dynamic research environment and make a tangible impact on patient lives. The ability to mentor and develop junior scientists will also be a key aspect of this leadership position.

Key Responsibilities:

• Lead the design, execution, and interpretation of clinical trials for novel drug candidates.
• Develop clinical trial protocols, Investigator's Brochures, and study reports.
• Oversee data analysis and ensure the scientific integrity of clinical study results.
• Provide scientific and strategic direction to clinical research teams.
• Collaborate with internal and external stakeholders, including regulatory bodies, investigators, and CROs.
• Ensure compliance with all relevant regulatory guidelines and ethical standards.
• Contribute to the development of regulatory submissions (e.g., IND, NDA).
• Present scientific findings at internal meetings and external conferences.
• Mentor and guide junior clinical research staff.
• Identify and evaluate new research opportunities and therapeutic areas.

Qualifications:

• Ph.D. or Master's degree in a relevant life science field (e.g., Pharmacology, Medicine, Biology, Biochemistry).
• Minimum of 7 years of progressive experience in clinical research within the pharmaceutical or biotechnology industry.
• Proven experience in clinical trial design, execution, and data analysis across various phases (Phase I-IV).
• In-depth knowledge of pharmaceutical R&D, regulatory affairs, and clinical trial methodology.
• Strong understanding of statistical principles applied to clinical trials.
• Excellent leadership, project management, and communication skills.
• Demonstrated ability to publish and present scientific data.
• Experience in specific therapeutic areas such as oncology, immunology, or cardiovascular diseases is highly desirable.
• Familiarity with Good Clinical Practice (GCP) guidelines.

Our client, a pioneering pharmaceutical company, is seeking a highly motivated and experienced Senior Clinical Research Scientist specializing in Oncology to join their dedicated research team in Los Angeles, California. This critical role focuses on the design, execution, and interpretation of clinical trials for novel cancer therapies. The ideal candidate will possess a deep understanding of oncology drug development, clinical trial methodologies, regulatory requirements, and statistical analysis. You will be instrumental in advancing the oncology pipeline, contributing to life-saving treatments for patients.

Key Responsibilities:

• Lead the scientific and operational aspects of clinical trials for oncology assets, from protocol development to final study report.
• Design clinical trial protocols, including study objectives, endpoints, patient selection criteria, and statistical analysis plans.
• Oversee the execution of clinical trials, ensuring adherence to Good Clinical Practice (GCP), regulatory guidelines, and ethical standards.
• Analyze and interpret complex clinical data, identifying trends, safety signals, and efficacy findings.
• Collaborate with cross-functional teams, including translational science, regulatory affairs, medical affairs, and biostatistics.
• Prepare clinical study reports, manuscripts for publication, and presentations for scientific conferences.
• Manage relationships with investigators, clinical research organizations (CROs), and other external partners.
• Contribute to the development of regulatory submissions (e.g., IND, NDA).
• Stay abreast of the latest scientific advancements and clinical research trends in oncology.

The successful candidate will hold a Ph.D. or M.D. in a relevant scientific discipline (e.g., Oncology, Pharmacology, Medicine) with a minimum of 5-7 years of experience in clinical research within the pharmaceutical or biotechnology industry, specifically focusing on oncology. Demonstrated experience in designing and leading Phase I-III clinical trials is required. Strong knowledge of oncology therapeutics, biomarkers, and current treatment landscapes is essential. Excellent scientific writing, presentation, and communication skills are mandatory. This role is based at our client's state-of-the-art facility in Los Angeles, California, US . We are seeking a driven and collaborative scientist who is passionate about translating scientific discoveries into meaningful treatments for cancer patients, contributing significantly to the company's mission to improve global health outcomes through innovative pharmaceutical development.

Our client, a pioneering biopharmaceutical company, is seeking a highly accomplished Senior Clinical Research Scientist specializing in Oncology to join their esteemed fully remote research team. This critical role will drive the design, execution, and interpretation of cutting-edge clinical trials aimed at developing novel cancer therapies. You will be instrumental in shaping the clinical development strategy, ensuring scientific rigor, and translating groundbreaking discoveries into life-saving treatments. This position offers the flexibility of remote work, allowing you to contribute from anywhere in the US.

Responsibilities:

• Lead the development of clinical trial protocols, ensuring scientific integrity, regulatory compliance, and alignment with strategic objectives.
• Provide scientific and medical expertise throughout the clinical trial lifecycle, from study design and site selection to data analysis and regulatory submission.
• Analyze and interpret complex clinical trial data, including efficacy, safety, and biomarker data, to inform decision-making and future development strategies.
• Collaborate closely with cross-functional teams, including preclinical research, regulatory affairs, medical affairs, statistics, and operations, to ensure seamless trial execution.
• Engage with key opinion leaders (KOLs) and investigators to foster strong relationships and gather critical scientific insights.
• Contribute to the preparation of scientific publications, abstracts, and presentations for major medical conferences.
• Evaluate new drug candidates and therapeutic strategies within the oncology space.
• Ensure adherence to Good Clinical Practice (GCP) guidelines and all applicable regulatory requirements.
• Mentor junior scientists and contribute to the overall scientific growth of the clinical development team.
• Stay abreast of the latest advancements in oncology research, including emerging targets, therapeutic modalities, and competitive landscape.

Qualifications:

• Ph.D. or M.D. in a relevant life science discipline (e.g., Oncology, Immunology, Molecular Biology, Pharmacology).
• Minimum of 6 years of experience in clinical research, with a significant focus on oncology drug development within the pharmaceutical or biotechnology industry.
• Deep understanding of oncology, cancer biology, and current treatment paradigms.
• Proven experience in designing and managing Phase I, II, and III clinical trials.
• Strong knowledge of regulatory requirements (FDA, EMA) and GCP guidelines.
• Excellent scientific writing and communication skills, with a demonstrated ability to present complex data clearly.
• Demonstrated ability to work independently and collaboratively in a remote team environment.
• Experience with biomarker strategy and analysis is highly desirable.
• Strong analytical and problem-solving skills.
• Track record of scientific contributions (publications, presentations).

This is an exceptional opportunity to make a profound impact on the lives of cancer patients worldwide.

Our client, a pioneering biopharmaceutical company, is seeking a highly experienced and innovative Lead Clinical Research Scientist specializing in Oncology to join their cutting-edge research division in Los Angeles, California, US . This is an on-site position requiring a deep understanding of cancer biology, clinical trial design, and regulatory affairs. The Lead Clinical Research Scientist will be instrumental in driving the development of novel oncology therapeutics from early-stage research through to clinical trials. You will collaborate with a multidisciplinary team of scientists, clinicians, and regulatory experts to advance our client's pipeline and bring life-saving treatments to patients.

Responsibilities:

• Design and oversee the execution of clinical trial protocols for oncology drug candidates.
• Analyze and interpret complex clinical trial data, translating findings into actionable strategies.
• Provide scientific and clinical expertise to cross-functional teams, including preclinical research, regulatory affairs, and medical affairs.
• Author and contribute to scientific publications, presentations, and regulatory submissions.
• Stay abreast of the latest advancements in oncology research, therapeutic approaches, and competitive landscape.
• Collaborate with key opinion leaders (KOLs) in the field of oncology.
• Contribute to the development of long-term research strategies and portfolio planning.
• Ensure compliance with all Good Clinical Practice (GCP) guidelines and relevant regulatory requirements.
• Manage budgets and resources for assigned clinical research projects.
• Mentor junior scientists and research staff.
• Participate in scientific conferences and meetings to represent the company and present research findings.
• Contribute to the identification and evaluation of new research opportunities and potential collaborations.

Qualifications:

• Ph.D. or M.D. in a relevant scientific discipline (e.g., Oncology, Immunology, Molecular Biology, Pharmacology).
• Minimum of 8 years of relevant experience in clinical research, with a significant focus on oncology drug development.
• Proven track record of designing and conducting Phase I-III clinical trials.
• Extensive knowledge of cancer biology, tumor immunology, and current oncology treatment paradigms.
• Strong understanding of GCP, regulatory guidelines (e.g., FDA, EMA), and drug development processes.
• Excellent analytical, statistical, and data interpretation skills.
• Exceptional scientific writing and presentation abilities.
• Proven ability to lead and motivate scientific teams.
• Strong collaboration and communication skills, with the ability to engage effectively with internal and external stakeholders.
• Experience with biostatistics and clinical trial data management systems.
• Ability to travel as needed for scientific meetings and site visits.

This critical role in Los Angeles, California, US demands a visionary scientist dedicated to making a profound impact on cancer treatment. Join a team committed to innovation and patient care, working at the forefront of pharmaceutical research. Our client offers a competitive compensation package, comprehensive benefits, and a stimulating research environment.

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.
**Working at Abbott**
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You'll also have access to:
+ Career development with an international company where you can grow the career you dream of .
+ Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
+ An excellent retirement savings plan with high employer contribution
+ Tuition reimbursement, the Freedom 2 Save ( student debt program and FreeU ( education benefit - an affordable and convenient path to getting a bachelor's degree.
+ A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
+ A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.
**The Opportunity**
This position works out of our **Sylmar, CA** location in the **Cardiac Rhythm Management** division.
As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats.
**Senior** **Principal** **Clinical** **Research** **Scien** **tist** **,** will be viewed as a leader on scientific and medical matters related to clinical trial design, clinical evaluations, risk management, strategy, management, and/or analysis of data. Expert in writing/managing clinical evaluation (plans and reports) or clinical trial protocols, risk master lists, clinical trial registrations and results postings, clinical study project timelines and scientific publications. Leads various study support groups and cross-functional teams in order to develop clinical strategy. Interacts with regulatory agencies as needed, and will use their scientific and medical knowledge in order to provide directives to teams as well as study sites. Be able to mentor other clinical scientists within Clinical Research.
**What You'll Work On**
+ Provide scientific leadership to the team, advising on different aspects of clinical evaluations and trial strategies, risk management, design, data analysis, and/or a variety of scenarios for a robust strategy and planning.
+ This position will require significant interactions with cross-functional teams within (Biostatics, RA, Clinical Operations, Data Management, Safety, Science, Clinical Affairs, etc) and outside (R&D, strategic marketing, Clinical R&D, Quality Engineering, Product Performance Group, Risk Management) clinical-regulatory organization, and some interactions with principal investigators in the trials.
+ Responsible for the delivery of the development of clinical evaluation plans or reports, and/or study protocols, the resulting reports and able to lead scientific discussions.
+ Interprets results in preparation for product applications by evaluating clinical and scientific and risk data and literature, and staying abreast of current clinical practice.
+ Presents scientific data by communicating accurate, succinct summaries of clinical results at industry gatherings, investigational meetings and regulatory agency meetings.
+ Facilitates regulatory submissions and communications by communicating with Regulatory Affairs during the submission process.
+ Participates in and supports audits.
+ Financial, budgetary, and legal interactions are expected as directed by the manager.
+ Responsible for compliance with applicable Corporate and Divisional Policies and procedures.
+ Will perform this job in a quality system environment.
**Required Qualifications**
+ Bachelors Degree in related field OR an equivalent combination of education and work experience
+ Minimum 10 years
+ At least 5 years of clinical trial, risk management, or clinical evaluation experience.
+ Comprehensive knowledge of specified functional area. Uses in-depth knowledge of business unit functions and cross group dependencies/ relationships. Is recognized as an expert in work group and across functions. Will perform this job in a quality system environment. Failure to adequately perform tasks can result in noncompliance with governmental regulations. Works on complex problems where analysis of situations or data requires an in-depth evaluation of various factors. Exercises judgment within broadly defined practices and policies in selecting methods, techniques and evaluation criteria for obtaining results. Has broad knowledge of various technical alternatives and their potential impact on the business.
Apply Now ( more about our health and wellness benefits, which provide the security to help you and your family live full lives:** ( your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at , on Facebook at and on Twitter @AbbottNews and @AbbottGlobal.
The base pay for this position is $146,700.00 - $293,300.00. In specific locations, the pay range may vary from the range posted.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email

Description
Coordinate day-to-day activities for clinical research studies across various therapeutic areas
Perform direct patient-facing duties, including informed consent, visit scheduling, and follow-up
Manage all aspects of patient recruitment and enrollment across studies, including database reviews, outreach, pre-screening, and communications
Confidently perform blood draws and handle biospecimen processing and shipping in accordance with protocol requirements
Maintain and manage study documentation, source data, and regulatory binders across numerous systems
Support monitoring visits and participate in both internal and external audits
Communicate effectively with sponsors, CROs, investigators, and internal departments
Provide general support to the team and step in across functions as needed to meet study goals
Additional Skills & Qualifications
Required Qualifications:
Minimum 3 years of clinical research coordinator (CRC) experience for industry-sponsored, interventional clinical trials for investigational drugs
Proficiency in patient care, regulatory management, lab specimen handling, monitoring, and auditing
Excellent multitasking, time management, and organizational abilities
Willingness and ability to travel regularly (up to 50%) across sites
Preferred Qualifications:
Fluent in Spanish (spoken and written)
Certified Clinical Research Coordinator (CCRC) certification
Prior experience with multi-site clinical trials or decentralized trial models
Familiarity with clinical trial management systems (CTMS) and electronic regulatory platforms
Flexibility, initiative, and a team-oriented mindset are essential
Candidates must be comfortable working in a fast-paced, high-accountability environment
Pay and Benefits
The pay range for this position is $31.00 - $40.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Los Angeles,CA.
Application Deadline
This position is anticipated to close on Oct 3, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.

Description
The Clinical Research Coordinator contributes to the overall
operational management of clinical research/trial/study activities from design,
set up, conduct, through closeout. The position has responsibility for the
implementation of research activities for one or more studies. The incumbent
recognizes and performs necessary tasks to manage projects and prioritizes work
to meet necessary deadlines. The incumbent is responsible for planning and
organizing necessary tasks to ensure adherence to the study protocol and
applicable regulations, such as institutional policy and procedures, FDA Code
of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP).
The Clinical Research Coordinator collaborates with the Principal Investigator
(PI), ancillary departments, central research infrastructure teams, sponsors,
institutions, and other entities as needed to support the administration of all
aspects of studies, including, but not limited
to, compliant conduct, financial management, and adequate personnel support.
_This is a 24 month, part-time limited position that may convert to career._
Salary Range: $33.63 - $54.11/HourlyQualifications
All Required:
+ Bachelors Degree or 1-3 years of previous study coordination or clinical research coordination experience.
+ Strong verbal and written communication skills along with strong interpersonal skills to effectively establish rapport, and build collaborate relationships.
+ Strong organizational capabilities to organize multiple projects and competing deadlines for efficiency and cost effectiveness.
+ Analytical skills sufficient to work and solve address problems and identify solutions with reasoned judgement.
+ Ability to adapt to changing job demands and priorities; work flexible hours to accommodate research deadlines.
+ Ability to respond to situations in an appropriate and professional manner.
+ Ability to concentrate and focus in a work environment that contains distracting stimuli and competing deadlines.
+ Ability to be flexible in handling work delegated by more than one individual.
+ Typing and computer skill/ability including word-processing, use of spreadsheets, email, data entry. Ability to navigate numerous software programs and applications.
+ Ability to handle confidential material information with judgement and discretion.
+ Working knowledge of the clinical research regulatory framework and institutional requirements.
+ Mathematical skills Sufficient to prepare clinical research budgets, knowledge of math ability and knowledge of clinical trials research budgeting process to assist with the preparation of clinical trial budgets.
+ Working knowledge of FDA Code of Federal Regulations (CFR) and ICH Good Clinical Practice (GC) for clinical research.
+ Be available to work in more than one environment, travel to meetings, off-site visits, conferences, etc.
UCLA Health welcomes all individuals, without regard to race, sex, sexual orientation, gender identity, religion, national origin or disabilities, and we proudly look to each person's unique achievements and experiences to further set us apart.

Description Coordinate day-to-day activities for clinical research studies across various therapeutic areas Perform direct patient-facing duties, including informed consent, visit scheduling, and follow-up Manage all aspects of patient recruitment and enrollment across studies, including database reviews, outreach, pre-screening, and communications Confidently perform blood draws and handle biospecimen processing and shipping in accordance with protocol requirements Maintain and manage study documentation, source data, and regulatory binders across numerous systems Support monitoring visits and participate in both internal and external audits Communicate effectively with sponsors, CROs, investigators, and internal departments Provide general support to the team and step in across functions as needed to meet study goals Additional Skills & Qualifications Required Qualifications: Minimum 3 years of clinical research coordinator (CRC) experience for industry-sponsored, interventional clinical trials for investigational drugs Proficiency in patient care, regulatory management, lab specimen handling, monitoring, and auditing Excellent multitasking, time management, and organizational abilities Willingness and ability to travel regularly (up to 50%) across sites Preferred Qualifications: Fluent in Spanish (spoken and written) Certified Clinical Research Coordinator (CCRC) certification Prior experience with multi-site clinical trials or decentralized trial models Familiarity with clinical trial management systems (CTMS) and electronic regulatory platforms Flexibility, initiative, and a team-oriented mindset are essential Candidates must be comfortable working in a fast-paced, high-accountability environment Pay and Benefits The pay range for this position is $31.00 - $40.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type This is a fully onsite position in Los Angeles,CA. Application Deadline This position is anticipated to close on Oct 3, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email for other accommodation options.

About Us:

Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.

Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full-time employees after 30 days of employment, including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.

Hourly Range: 20.00 - 23.00/hr ( Depending on education, experience, and skillset)

We have 2 shifts available ( 8:00 am to 4:30 pm, OR 8:30 am to 5:00 pm)

• Monday - Friday + must be able to work rotating weekends.

Job Summary:

With moderate oversight, the Pharmacy Technician I will assist in providing support of clinical investigational drug trials; provide accurate and efficient dispensing of medication, and perform cross-functional duties as required.

Essential Responsibilities and Duties:

• Monitors pharmacy activities daily to ensure adherence to study protocols and dispensing procedures.
• Prepare and dispense investigational drugs in accordance with the IRB-approved protocols under the supervision of the Pharmacist or site management.
• Assist Pharmacist or site management in preparing blinded study products.
• Ensure the appropriate storage of investigational drugs according to the protocol and FDA guidelines.
• Monitor temperature of pharmacy storage areas and alert Pharmacist or site management of any temperature excursions of study drug.
• Assists in ordering, receiving, unpacking and storing pharmaceuticals and supplies.
• Rotates stock to ensure use before expiration date.
• Monitors expiration date and supply of drug for clinical trials.
• Prepares medication for dispensing to patients enrolled in inpatient study protocols.
• Supports and ensures strictest adherence to best practices, FDA Code of Federal Regulations, ICH (International Conference on Harmonization), GCP (Good Clinical Practices), CenExel standard operating procedures, site working Practices, protocol, and company guidelines and policies.
• Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.

Education/Experience/Skills:

• Must be able to effectively communicate verbally and in writing.
• Certified Pharmacy Technician required.
• Minimum of 1 year related experience preferred.
• Knowledge of basic pharmacy practices and procedures.
• Knowledge of medications and medical supplies.
• Ability to maintain quality control standards.
• Ability to react calmly and effectively in emergency situations.
• Ability to interpret, adapt, and apply guidelines and procedures.
• Attention to detail.

Working Conditions

1. Indoor, Clinic environment.
2. Essential physical requirements include sitting, typing, standing, walking.
3. Lightly active position, occasional lifting of up to 20 pounds.
4. Reporting to work, as scheduled, is essential.
5. On-site work arrangement.

CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.

Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.