Top 87 Research associate Jobs in Houston, Tx

Experienced Clinical Research Associate (Level II) - FSP - Alzheimer's - Central US
Thermo Fisher Scientific —Texas
- Full-time
- Hybrid work
- Nursing
- RN License
- Writing skills
Post Doctorate Research Associate
ExxonMobil —Spring, TX
- Office
- Analysis skills
- Doctor of Philosophy
Research Assistant I
MD Anderson —Houston, TX
- $18.99 - $28.61 an hour
- Full-time
- No experience needed
- Master's degree
- Bachelor's degree
- AD&D insurance
- Paid holidays
Research Associate (Path & Lab)
UTHealth Houston —Houston, TX
- Mid-level
- 3 years
- Master's degree
- Health insurance
- Employee discount
Research Associate
Texas A&M University —Houston, TX
- 8 hour shift
- Mid-level
- University
- Bachelor's degree
- AD&D insurance
- Paid holidays
Research Associate 2
University of Houston —Houston, TX
- Full-time
- Mid-level
- 3 years
- Analysis skills
7d
Research Associate 1
University of Houston —Houston, TX
- Full-time
- Mid-level
- Analysis skills
- University
7d
Design Research Associate
Midstream & Terminal Services —Houston, TX
- $55,000 - $60,000 a year
- Management
- Public speaking
- Mid-level
Research Assistant I
Houston Methodist Academic Institute —Houston, TX
- Full-time
- Hospital
- No experience needed
- English
3d
Consulting Associate, Environmental Scientist (Assistant Wetland Delineator)
ERM Group —Houston, TX
- Full-time
- Hybrid work
- Bachelor of Science
- Master's degree
- Driver's License
5d
Research Assistant II
MD Anderson —Houston, TX
- $21.63 - $32.69 an hour
- Full-time
- No experience needed
- Mid-level
- Master's degree
- AD&D insurance
- Paid holidays
Research Technician - Rooney CAGT
Houston Methodist Academic Institute —Houston, TX
- Full-time
- Hospital
- No experience needed
- English
Senior Clinical Research Associate (level dependent on experience)
CTI Clinical Trial Services, Inc —Houston, TX
- Hybrid work
- Nursing
- Mid-level
- Master's degree
- Paid parental leave
- Tuition reimbursement
Quick Apply
Research Assistant I (Part Time) - Integrative Biology and Pharmacology
UTHealth Houston —Houston, TX
- Part-time
- No experience needed
- Bachelor's degree
- Entry level
- Health insurance
- Employee discount
4d
Research Assistant I-CHG-The Brown Foundation Institute of Molecular Medicine
UTHealth Houston —Houston, TX
- No experience needed
- Bachelor's degree
- Communication skills
- Health insurance
- Employee discount
4d
Research Technician I
Rice University —Houston, TX
- $18.00 - $21.19 an hour
- Overtime
- Writing skills
- Databases
- High school diploma or GED
14d
Research Assistant I-CTCR--The Brown Foundation Institute of Molecular Medicine
UTHealth Houston —Houston, TX
- Writing skills
- No experience needed
- Bachelor's degree
- Health insurance
- Employee discount
10d
Equity Research Associate- E&P (Energy)
Raymond James Financial, Inc. —Houston, TX
- Full-time
- Writing skills
- Mid-level
- Analysis skills
- Paid holidays
- Health insurance
11d
Research Assistant I - Psychological Intervention and Research Laboratory for Mood Spectrum Disorders/UT Brain Collection
UTHealth Houston —Houston, TX
- Psychiatry
- No experience needed
- University
- Health insurance
- Employee discount
Senior Clinical Research Associate
Immatics US —Houston, TX
- $120,000 - $135,000 a year
- Full-time
- Background check
- Nursing
- Pass drug screening
- Paid parental leave
- Paid holidays

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Experienced Clinical Research Associate (Level II) - FSP - Alzheimer's - Central US

Thermo Fisher Scientific -
Texas

Apply Now

Job Details

Full-time

Qualifications

Customer communication
Driver's License

Full Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.

As part of our global team, you’ll have the opportunity to perform and coordinate all aspects of the clinical monitoring and site management process. As a Clinical Research Associate (Level II), you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation. You will manage procedures and guidelines from different sponsors and/or monitoring environments (i.e., FSO, FSP, Government, etc.). Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability. You will ensure audit readiness and develop collaborative relationships with investigational sites. Detailed tasks and responsibilities assigned to your role are outlined in the task matrix.

What You’ll Do:

Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site and remote monitoring activities. Assess investigational product through physical inventory and records review. Documents observations in reports and letters in a timely manner using approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner. Conducts monitoring tasks in accordance with the approved monitoring plan. Participates in the investigator payment process. Ensures a shared responsibility with other project team members on issues/findings resolution. Investigates and follows-up on findings as applicable.
Participates in investigator meetings as necessary. Identifies potential
investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Performs trial close out and retrieval of trial materials.
Ensures that required essential documents are complete and in place, according to ICH-GCP and applicable regulations. Conducts on-site file reviews as per project specifications.
Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are updated per agreed study conventions (e.g. Clinical Trial Management System).
Facilitates effective communication between investigative sites, the client company and the PPD project team through written, oral and/or electronic contacts.
Responds to company, client and applicable regulatory requirements/audits/inspections.
Maintains & completes administrative tasks such as expense reports and timesheets in a timely manner.
Contributes to the project team by assisting in preparation of project publications/tools, and sharing ideas/suggestions with team members.
Contributes to other project work and initiatives for process improvement, as required.

Education and Experience Requirements:

Bachelor's degree in a life sciences related fieldor a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification.
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 1 years as a clinical research monitor) or completion of PPD Drug Development Fellowship.
Valid driver's license where applicable.

In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills and Abilities:

Proven clinical monitoring skills
Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
Demonstrated ability to attain and maintain a working knowledge of ICH GCPs, applicable regulations and procedural documents
Well-developed critical thinking skills, including but not limited to: critical mindset, in-depthinvestigation for appropriate root cause analysis and problem solving
Ability to manage Risk Based Monitoring concepts and processes
Good oral and written communication skills, with the ability to communicate effectively with medical personnel
Ability to maintain customer focus through the utilization of good listening skills, attention to detail and the ability to perceive customers’ underlying issues
Good organizational and time management skills
Effective interpersonal skills
Attention to detail
Ability to remain flexibile and adaptable in a wide range of scenarios
Ability to work in a team or independently as required
Good computer skills: solid knowledge of Microsoft Office and the ability to learn appropriate software
Good English language and grammar skills
Good presentation skills

Working Conditions and Environment:

Work is performed in an office/ laboratory/clinical/and/or home office environment with exposure to electrical office equipment.
Frequent drives to site locations. Frequent travel, generally 60-80% but more for some individuals. May also include extended overnight stays.
Exposure to biological fluids with potential exposure to infectious organisms.
Personal protective equipment required such as protective eyewear, garments and gloves.
Exposure to fluctuating and/or extreme temperatures on rare occasions

Apply Now

Refine Your Search

research associate jobs in houston, tx

Experienced Clinical Research Associate (Level II) - FSP - Alzheimer's - Central US

Post Doctorate Research Associate

Research Assistant I

Research Associate (Path & Lab)

Research Associate

Research Associate 2

Research Associate 1

Design Research Associate

Research Assistant I

Consulting Associate, Environmental Scientist (Assistant Wetland Delineator)

Research Assistant II

Research Technician - Rooney CAGT

Senior Clinical Research Associate (level dependent on experience)

Research Assistant I (Part Time) - Integrative Biology and Pharmacology

Research Assistant I-CHG-The Brown Foundation Institute of Molecular Medicine

Research Technician I

Research Assistant I-CTCR--The Brown Foundation Institute of Molecular Medicine

Equity Research Associate- E&P (Energy)

Research Assistant I - Psychological Intervention and Research Laboratory for Mood Spectrum Disorders/UT Brain Collection

Senior Clinical Research Associate

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