Clinical Research Staffing stock photo
March 17th, 2017

GVP Pharmacovigilance Audits – Senior GVP Audit/Project Manager Needed

Our client needs a full-time Senior GVP Audit/Project Manager to handle their GVP Pharmacovigilance Audits. This person will plan and perform domestic and international GVP audits to assess the company’s compliance to local and international government regulations. They will also assess internal SOPs as they relate to GVP Quality Assurance and regulatory compliance. This position is located Read the rest of this entry »

March 2nd, 2017

Clinical Operation Manager Needed, Remote / Work from Home

Clinical Operation Manager needed by our client to co-ordinate clinical study design and implementation at a program and functional level according to Good clinical practice (GCP).

Clinical Operation Manager Qualifications

  • Position requires a minimum of a Bachelor of Science degree and at least 5 years of clinical study management experience, including at least 2 years of phase III study management experience (7 years of clinical management experience for Sr. Manager or graduate level education with at least 3 years of clinical study management experience) in clinical research within a pharmaceutical or biotech environment or relevant CRO experience.
  • Experience working in therapeutic areas in ophthalmology will be a plus.
  • Good understanding of clinical study implementation process.
  • Willingness to travel up to 30%, as necessary, consistent with study or functional needs.

Read the rest of this entry »

February 17th, 2017

Oncology Medical Writer Needed, Remote Work

Our client is in need of an experienced oncology medical writer. The medical writer will translate the scientific hypotheses of clinical trials into lay terms for patient population and patient navigators. Ideally, you have experience in consumer-facing communication.

The client is developing software to better match stage Read the rest of this entry »

February 10th, 2017

QA Engineer – Medical Devices & IVD Manufacturer, Los Angeles, CA

QA Engineer needed to manage the selection, qualification, and monitoring of suppliers including finished device, OEM, and contract manufacturers. This person will play a key role in working with suppliers to resolve quality issues (SCAPAs), resolving internal non-conforming product issues, addressing incoming inspection challenges, including development and review of inspection procedures, overseeing equipment calibration, maintenance and validation, and maintaining accurate and complete documentation of these activities in compliance with the requirements of the Quality System Regulation (21 CFR 820) and ISO 13485.


  • B.S. in in a technical discipline (i.e. science or engineering)
  • Five or more years of relevant experience in an FDA regulated industry
  • 3-5 years of which is in Quality Assurance
  • ASQ Certification as Quality Engineer (CQE) or equivalent, preferred

Read the rest of this entry »

February 3rd, 2017

Senior Regulatory Affairs Associate

(Chicago Area, IL)



This position is ideal for Ideal for someone looking to lead Regulatory strategy at the company’s facility located in the Chicago area.


This Regulatory Affairs Professional will be responsible for:

February 1st, 2017

Laboratory Assistant – Medical Devices & IVD Manufacturer, Los Angeles, CA

Laboratory Assistant needed to perform routine equipment maintenance, assure adequate stock and labeling of laboratory reagents and consumables, manage chemical and biological waste, sanitize lab surfaces, and monitor environmental controls.


  • B.S. in Chemistry, molecular biology or biological sciences
  • 1-4 years hands-on experience in a regulated, laboratory environment
  • Knowledge of GLP, CLIA and HIPAA regulations governing handling and testing of patient samples in a clinical lab
  • Knowledge of safety precautions required for working with blood borne pathogens
  • Medical background preferred which includes medical terminology applicable to a clinical laboratory

Read the rest of this entry »

January 28th, 2017

VP Clinical Development – Rare and Orphan Diseases

VP Clinical Development for a small clinical-stage pharma company in Los Angeles San Fernando Valley. Candidate needs to have a MD, be experienced in rare and orphan disease studies and have significant experience clinical trials.



  • M.D. or D.O. with specialty training, preferably CNS diseases
  • 10 -15 years of progressive experience through all the phases of drug development would be ideal
  • Management of clinical trials (Phases 1 – 3)
  • Experience in orphan and rare diseases, pediatrics and/or neurology preferred

Read the rest of this entry »

January 26th, 2017

Product Development Engineer- Medical Devices & IVD Manufacturer, Los Angeles, CA

Product Development Engineer needed to oversee the development and manufacture of low cost, plastic devices including disposable blood collection devices.


  • At least 5 years of experience in the development of medical devices
  • Bachelor’s degree in an engineering discipline preferred.
  • Mechanical and/or electrical engineering background
  • Experience in manufacturing, development, project management or commercial roles in a regulated (FDA, ISO) manufacturing environment.
  • Computer aided design (CAD) / SolidWorks or similar software package

Additional Expertise: Knowledge & Skills

January 24th, 2017

VP Genomic Research, Los Angeles CA

VP Genomic Research needed to manage operational and logistical tasks of genomic test development to ensure efficient execution of studies for molecular diagnostic products within established budgets and timelines, ensuring all activities occur in compliance with the appropriate regulations.  The candidate will be responsible for designing the test development process, directing a team of molecular biologist, computational biologists, and clinical scientists. Read the rest of this entry »

January 23rd, 2017

Director of IVD Manufacturing and Supply Chain

Director of IVD Manufacturing and Supply Chain needed for an in-vitro diagnostics (IVD) client in Los Angeles, CA. The role is responsible for working with Product Development to select and manage key suppliers. Work alongside management and sales to establish forecasts and delivery schedules for key materials. This role will also negotiate Supply Contracts and assist in Read the rest of this entry »

January 21st, 2017

VP Clinical Affairs needed in Los Angeles, CA

VP Clinical Affairs needed to develop and implement clinical studies and molecular diagnostics validation strategy. The VP will coordinate the efforts of internal and external resources to ensure fast patient recruitment, trial site selection, trial plan optimization, and execution of trials with a focus on data quality. The candidate must be Read the rest of this entry »

September 27th, 2016

Top 25 Biotech Companies – Career Search

The Top 25 biotech companies have convoluted career sites. It is frequently difficult to find where to search jobs and often more complicated than it needs to be.

Career Search All of Them at Once

Genetic Engineering and Biotechnology News (GEN) published a list of the Top 25 Biotech companies. Their list is based on total market capitalization. Interested in searching for your next job at these top companies? Use our search engine below. Tweet: Easier way to #jobsearch the top 25 #biotech companies. Use this search engine @meirxrs #clinicalresearch #pharma It only includes career pages of the companies that made GEN’s list*.
Read the rest of this entry »

August 19th, 2016

Oncology Research Nurse

An Oncology Research Nurse is needed by our client in Santa Monica, CA. Candidate should have experience in Oncology and wants grow by serving patients enrolled in clinical trials. Read the rest of this entry »

August 3rd, 2016

Business Development / Sales -Cardio Medical Devices

Business Development, Sales Manager, or Account Manager with more than 5 years of experience selling to the cardiovascular medical device industry needed. The position calls for someone to sell auditing and testing services to medical device companies. The candidate should demonstrate they have built a book of business within the medical device industry and increased revenues. Read the rest of this entry »

July 12th, 2016

Clinical Research Services

Clinical Research Services help optimize your development timelines, whether your company is developing a biologic, drug or medical device. We offer a range of services to help you achieve your objectives.

We have separate legal entities (staffing, recruiting and CRO). Each helps you solve your Read the rest of this entry »

June 16th, 2016

Biotechnology Jobs vs Biotechnology Careers

Biotechnology jobs are for short-term goals.

Biotechnology careers include your long-term goals. You can manage this journey through a combination of education, certifications and experience. Only then can you arrive at the destination you are most interested in.

Biotechnology jobs includeClinical Trials, Clinical Research, Quality, Regulatory, and Medical Affairs, Engineering and Software. Research in food, pharmaceuticals, biologics, and medical devices are sometimes lumped in with biotechnology.Keywords for biotechnology jobs and biotechnology careers


Skip to Search for Jobs


Let’s begin your career progression with Read the rest of this entry »

May 17th, 2016

Commercial Development Director / Sales (East Coast, West Coast, Europe)

The Commercial Development Director will set a road map for the sales team. The client is a Contract Manufacturer that provides bulk drug formulation and manufacturing. They also provide primary and secondary packaging capabilities for solid dose drugs. Their technologies include granulation, coating, blending, encapsulation, compression and drying of tablets and capsules.

Preferred Experience

  • Bachelor’s Degree Science/Business
  • Five plus years of selling in the Contract Manufacturing market
  • Operational Experience

Read the rest of this entry »

May 13th, 2016

Director Account Management – Southern California

The Director Account Management will help establish pharmacies in clinics. Read the rest of this entry »

March 11th, 2016

Clinical Project Manager (Part-Time Contract ) – Philadelphia, PA

A Clinical Project Manager (part time contract) is needed for a Contract Research Organization (CRO) to work in their office in the Philadelphia area. This position will report directly to the Chief Medical Officer and includes responsibility for coordinating and managing all aspects of clinical study activities to maintain regulatory compliance and meet company timelines and goals for the clinical development program.  Looking for Read the rest of this entry »

February 2nd, 2016

Clinical Affairs Director – TX or Upper Midwest

Clinical Affairs Director will lead and manage the Clinical Affairs Department globally, reporting to Read the rest of this entry »

January 20th, 2016

Clinical Studies Manager – Austin, TX

Clinical Studies Manager plays a major role in coordinating clinical studies, from qualification of clinical study sites through monitoring of clinical study activities and completion of Read the rest of this entry »

January 9th, 2016

Clinical Pharmacist, Los Angeles


January 8th, 2016

VP Clinical Operations in San Diego, CA

Education & Experience:

January 8th, 2016

VP Medical Affairs in San Diego

Education & Experience:

January 7th, 2016

Medical Device Compliance Auditor for Boston or Minneapolis Area

Medical Device Quality and Regulatory Compliance professionals needed for two opportunities to assess non-active medical devices and their manufacturers per the European Medical Devices Directives, other applicable Regulatory Systems and International standards, including related client and project management

  • 50% Audit
  • Perform regulatory audits of clients per European Medical Device Directives (AIMD, MDD, IVDD), Canadian Medical Device Regulations (CMDR), Japanese Pharmaceutical Affairs Law (JPAL) and International quality system standards (e.g. ISO 13485)
  • 50% Technical Document Review
  • Perform evaluations of regulatory submissions including: Clinical, Design Dossier, Technical File Review

Read the rest of this entry »

November 13th, 2015

GMP Regulations for Friday the 13th

Happy Friday the 13th! Remember, if you need a GMP or Quality specialist who knows the regulations below then don’t be scared. Call MEIRxRS. Read the rest of this entry »

November 11th, 2015

Quality Apprenticeship Program Featured on

Quality Apprenticeship on website

Quality Apprenticeship on website

The State of California, Department of Industrial Relations has listed our two Quality Apprenticeships: Chemistry Quality Control Technician and Microbiology Quality Control Technician. These represent two out of the three apprenticeships available in the Health Services category.

The Division of Apprenticeship Standards (DAS) creates Read the rest of this entry »

October 7th, 2015
FSMA Food Safety Modernization Act

FSMA Food Safety Modernization Act ensures the quality and safety of our food supply.

FSMA Half Day Workshop Attendees Give 4.6 Stars

Did you make the QLN FSMA half day workshop in Irvine? The 97 attendees seemed extremely satisfied with the Sept 24th, 2015 event, giving it an overall rating of 4.6 (scale 1-5).

Easy FSMA Launched

EasyFSMA website was launched by the Quality Leadership Network (QLN) members, which includes Rosemarie Christopher, our CEO. as a venue to disseminate information about the Food Safety Modernization Act (FSMA) and other Read the rest of this entry »

September 30th, 2015

Director of Quality GCP in San Diego, CA

We are searching for a Director of Quality GCP in San Diego, CA for a client in Phase III Trials. Candidates must have at least 4 years of experience in GCP to be considered.

Read the rest of this entry »

September 8th, 2015
Sample Clinical Trial Timeline used by Clinical Planning Manager

Sample Clinical Trial Manager Timeline

Sr. Clinical Planning Manager

Large Pharma Client Needs Your Clinical Trial Expertise!

A Clinical Planning Manager, capable of handling 12 teams with 25 members each of both internal and external members, is urgently needed by our client. You will use your 8 + years of industry experience to proactively identify potential pitfalls and steer the team around them. You will Read the rest of this entry »

August 17th, 2015

FSMA Compliance Workshop 2015


FSMA Compliance Workshop

Download the PDF flyer

FSMA will impact your food business. Find out how and what to do about it. This is a free half day workshop on Food Safety and Modernization Act (FSMA) compliance.

Breakfast and refreshments are sponsored by the American Society for Quality (ASQ) Food, Drug & Cosmetic Division, the Quality Leaders Network (QLN) Food Group, RxRS Apprenticeship Program and Food Safety Net Services.


FSMA is designed to ensure food quality from the farm to fork. FSMA requires all Read the rest of this entry »

July 22nd, 2014

Oncology Research Nurses (Contract/Perm)

Immediate need for experienced Oncology Research Nurses to work at a large clinical trial site in Los Angeles.

1) One Nurse is needed to fulfill a 3-4 month contract
2) Second Nurse is needed as a full-time direct hire Read the rest of this entry »

October 7th, 2013



The Food Science and Nutrition Department at Cal Poly, San Luis Obispo, CA is seeking a full-time, academic year, tenure-track position beginning January 6, 2013. For details, qualifications, and application instructions (online faculty application required), visit WWW.CALPOLYJOBS.ORG and refer to Requisition #102980 . Review Begin Date: October 15, 2013. EEO

May 15th, 2013

Business Development Professional, Los Angeles CA

Qualified candidate should have a measure of success in building clinical trials services
• Establish new accounts
• Coordinate with Site Director to assure alignment between sales and execution of clinical trials
• Develop strategic alliances with large accounts
• Collaborate with CEO and Site Director to develop plans to expand into new therapeutic areas
• Bachelor’s degree in Business Management, Marketing or related field and at least five years related experience
Clinical Research Organization experience preferred OR
• Relevant sales of Clinical Research Services
Please contact:
~position closed~

May 15th, 2013

Manager of Regulatory Affairs, Orange County CA

Job Description
• Manage Regulatory Affairs activities to include, but not limited to:
o Canadian Regulatory Submissions
o International Regulatory Submissions Teams
o Emerging Market Regulatory Strategy
o Global Product Assessments and Approvals
o Product Development Teams
o Regulatory Guidance for
 Change Control
 Product Review Boards

• BS degree minimum in life sciences, advanced degree preferred
• 8+ years of experience in medical device industry
• FDA and Global Regulation requirements for Medical Device product lifecycle
Please contact:
Lewie Casey
Talent Manager
Phone: 818-552-4173

May 15th, 2013

Director of Regulatory Affairs, Orange County CA

Job Description
• Direct Regulatory Affairs activities to include, but not limited to:
o Domestic and Global Regulatory Intelligence
o Regulatory Strategy
o Regulatory Communication
o Global Read the rest of this entry »

May 15th, 2013

Ph.D. Peptide-Synthesis Chemist, Los Angeles CA

Ph.D. peptide-synthesis chemist to produce, purify, and package synthetic peptides. The ideal candidate would have demonstrable experience in modern, automated peptide synthesis and HPLC purification, as well as a strong background in organic chemistry. Pharmaceutical or biotech experience highly desired.

Jan Clements
Talent Manager

May 15th, 2013

PhD Scientist –  Los Angeles, CA

Ph.D. scientist to perform analytical work and manage an analytical laboratory. The ideal candidate would have demonstrable experience managing a medium- to high-volume analytical lab in California, in either the biotech, pharmaceutical, or a related field, and also broad knowledge of modern analytical and instrumental methods.


~position closed~

May 15th, 2013

Sr. Manager/Director of Medical Education – Orange County, CA

As part of Global Medical Affairs, the Sr. Manager/Director of Medical Education is responsible for the successful execution of company Medical Affairs programs, including:

• Plan, manage and execute company’s New Customer Training and certification program worldwide, implement Staff and Surgeon training modules, develop strategies for training global field team.
• Associated to training and monitoring activities, the candidate will support implementation and execution of company’s podium and evidence plan, including:
o Planning, design, and execution of Read the rest of this entry »

May 8th, 2013

Clinical/Regulatory Medical Writer, Los Angeles CA

This position is for a medical writer with clinical and regulatory writing experience (not preclinical) and  will be based at Headquarters in the Los Angeles area (not home-based). Write clinical study reports, data summary reports, publications and promotional materials.


May 8th, 2013

Sr. Biostatistician, Los Angeles CA

This position oversees statistical aspects of assigned projects and provides support in study design, statistical analysis, and reporting of data. Plans, organizes, coordinates, and reviews activities of biostatistics activities. Read the rest of this entry »

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