ZipRecruiter

Log In

1

Fda Researcher Jobs in Spring, TX (NOW HIRING)

DM CLINICAL RESEARCH GROUP

CRC II (4268)

Tomball, TX · On-site

$23 - $30.50/hr

The Clinical Research Coordinator II will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP ...

DM CLINICAL RESEARCH GROUP

CRC II (3996)

Houston, TX · On-site

$21.75 - $29/hr

The Clinical Research Coordinator II will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP ...

DM Clinical

Site Manager (4138)

Houston, TX · On-site

The Site Manager's job is to ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide ...

previous page

Showing results 41-60

All JobsFda Researcher JobsFda Researcher Jobs in Spring, TX

Fda Researcher information

See Spring, TX salary details

$26.7K

$100.6K

$146.4K

How much do fda researcher jobs pay per year?

As of Sep 15, 2026, the average yearly pay for fda researcher in Spring, TX is $100,648.00, according to ZipRecruiter salary data. Most workers in this role earn between $59,600.00 and $137,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an FDA researcher?

To thrive as an FDA Researcher, you need a strong background in biological sciences, chemistry, or a related field, often supported by an advanced degree (MS or PhD). Familiarity with laboratory information management systems (LIMS), regulatory databases, and compliance certifications such as Good Laboratory Practice (GLP) is typically required. Critical thinking, attention to detail, and clear scientific communication are vital soft skills in this role. These competencies are essential for ensuring research integrity, regulatory compliance, and the advancement of public health.

What are some common challenges FDA researchers face when conducting regulatory studies?

FDA researchers often encounter challenges related to balancing scientific rigor with regulatory timelines. Strict protocols and documentation requirements can make study design and execution more complex, especially when coordinating with multiple stakeholders such as review teams and external partners. Additionally, researchers must stay updated on evolving regulatory guidelines and policies, which requires ongoing professional development. Effective communication and adaptability are key to overcoming these obstacles while ensuring that research supports public health objectives.

How much do FDA researchers make?

FDA researchers typically earn a median annual salary of around $70,000 to $120,000, depending on experience, education, and specific role. Entry-level positions may start lower, while senior or specialized roles can exceed this range, often requiring relevant scientific or regulatory expertise.

What does a FDA researcher do?

An FDA researcher conducts scientific studies and analyzes data related to food, drugs, medical devices, or cosmetics to ensure safety and efficacy. They often work in laboratories, review research protocols, and collaborate with regulatory teams to support approval processes and policy development.

What are popular job titles related to Fda Researcher jobs in Spring, TX?

For Fda Researcher jobs in Spring, TX, the most frequently searched job titles are:

What job categories do people searching Fda Researcher jobs in Spring, TX look for?

The top searched job categories for Fda Researcher jobs in Spring, TX are:

What cities near Spring, TX are hiring for Fda Researcher jobs?

Cities near Spring, TX with the most Fda Researcher job openings:

Fda Researcher jobs near you

Sub Investigator (NP)

Houston, TX • On-site

Dm Clinical Research Group
See more jobs at Dm Clinical Research Groupexternal

$44K - $44K/yr

Other

Posted 13 days ago

Job description

The Sub-Investigator (Nurse Practitioner) is accountable and responsible for ensuring adherence to protocol requirements, protecting the rights and welfare of subjects, assuring the integrity of subject generated data and directing the conduct of research according to federal and state regulations and guidance documents.DUTIES & RESPONSIBILITIESCompleting DMCR-required training, including GCP and IATA.Maintaining a working knowledge of current FDA regulations, GCP/ICH guidelines, organizational SOPs, guidance documents, and study protocols.Maintaining a current, up-to-date curriculum vitae and current licensure to practice.Assisting in managing the activities and performance of the clinical staff affiliated with the site.Performing clinical-related procedures and/or making important trial-related decisions delegated by the Principal Investigator.Performing clinical safety assessments and monitoring for study trial participation to include such items as: physical exams, EKGs, phlebotomy, and lab work evaluationPossessing a thorough understanding of the requirements of each protocol.Managing the medical care of subjects; protecting the rights and welfare of subjects.Ensuring documentation of study-related procedures, processes, and events.Attending investigator meetings as necessary for study participation.Any other matters as assigned by managementKNOWLEDGE & EXPERIENCEEducation:Bachelors or Masters in NursingExperience:Previous clinical research experienceNursing experience in a clinical settingCredentials:Current nursing licensure in good standing (Physician Assistant or Nurse Practitioner)Knowledge and Skills:Basic clinical and patient care skillsKnowledge of nursing and medical principles and techniquesClinical research knowledgeStrong communication skills, both written and verbalStrong diagnostic skillsEthical and legal healthcare principles in patient careProficient communication and comprehension skills both verbal and written in the English language are required.Proficient Bi-lingual (English/Spanish) communication and comprehension skills both in verbal and written are preferred. #J-18808-Ljbffr

Apply