Top 25 Clinical manager Jobs in Edinburg Tx

Clinical Research Coordinator
Pinnacle Clinical Research —Edinburg, TX
- Full-time
- Spanish
- Vital signs
- BLS Certification
- Paid holidays
- Disability insurance
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10d
Clinical Research Coordinator (Contract)
Pinnacle Clinical Research —Edinburg, TX
- Contract
- Spanish
- Vital signs
- BLS Certification
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10d
Clinical Nurse Coordinator Emergency Room
Rio Grande Regional Hospital —McAllen, TX
- Full-time
- Surgery
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Clinical Sales Specialist, Surgical Pain - Houston, TX
Avanos Medical —Texas
- $65,000 - $75,000 a year
- Full-time
- Remote
- Nursing
- Mid-level
- Windows
- Health insurance
- 401(k) matching
Clinical Registered Nurse Coordinator FSED
Rio San Juan FSED —San Juan, TX
- Full-time
- Mid-level
- Children
- Pediatrics
- Employee stock purchase plan
- Disability insurance
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Clinical Sales Specialist, Interventional Pain - North Texas (DFW, TX)
Avanos Medical —Texas
- $80,000 - $95,000 a year
- Full-time
- Remote
- Marketing
- Mid-level
- Windows
- Health insurance
- 401(k) matching
Clinical Nurse Coordinator Freestanding ED
Rio San Juan FSED —San Juan, TX
- Full-time
- Mid-level
- Children
- Pediatrics
- Employee stock purchase plan
- Disability insurance
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8d
Clinical Patient Navigator- Medical Office Coordinator
Healogics —Edinburg, TX
- $16.17 - $19.84 an hour
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Surgery
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14d
Clinical Behavioral Manager - FT - Days - BH Admin
DHR Health —Edinburg, TX
- Full-time
- Nursing
- RN License
- Customer service
LVN QI Coordinator -PT Days - Clinical Certification
DHR Health —Edinburg, TX
- Part-time
- Acute care
- Spanish
- LVN
NPST Clinical Operations Manager
Nurse Practitioner Services of Texas —Weslaco, TX
- Weekends as needed
- Nursing
- RN License
- Computer literacy
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Assistant Clinical Director
Empower Behavioral Health —Edinburg, TX
- $85,000 - $90,000 a year
- 8 hour shift
- Experience working with individuals with developmental disabilities
- Ability to walk for extended periods
- Mid-level
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Clinical Social Worker
Texas Oncology —McAllen, TX
- Full-time
- Spanish
- Master of Social Work
- Management
- Wellness program
- Disability insurance
RN Clinical Liaison
Gentiva —McAllen, TX
- Full-time
- CPR Certification
- Nursing
- Management
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Clinical Nurse Coordinator RN Day Surgery
Rio Grande Regional Hospital —McAllen, TX
- Full-time
- Surgery
- Mid-level
- Children
- Employee stock purchase plan
- Disability insurance
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Clinical Nurse Coordinator Special Care Unit
Rio Grande Regional Hospital —McAllen, TX
- Full-time
- Mid-level
- Children
- Employee stock purchase plan
- Disability insurance
Quick Apply
Clinical Donation Coordinator I - PeeDee Region
WE ARE SHARING HOPE SC —United States
- On call
- Mid-level
- Operating room
- 2 years

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Clinical Research Coordinator

Pinnacle Clinical Research -
Edinburg, TX

Quick Apply

Job Details

Full-time
10 days ago

Benefits

Paid holidays
Disability insurance
Health insurance
Dental insurance
401(k)
Flexible spending account
Paid time off
Vision insurance
Life insurance

Qualifications

BLS Certification
High school diploma or GED
ICH guidelines
Clinical quality assurance standards
Cross-functional communication

Full Job Description

Summary: The Clinical Research Coordinator will manage the day-to-day operations of assigned clinical trials and ensure that pre-established work scope, study protocol, and regulatory requirements are followed. They will recruit and screen study participants, document and report on the daily operations of a study, and report on participant status. This person must be able to understand clinical trial priorities and establish a workflow to complete all required activities promptly. This position is responsible for a broad range of duties involving confidential information. Strong communication and organizational skills are essential, along with a proactive, problem-solving mindset.

The Clinical Research Coordinator must be organized, excel at multi-tasking, detail-oriented, an excellent communicator, and be able to provide high-quality participant care. This person will collaborate very closely with other members of the team, pharmaceutical sponsors, and external vendors, and, therefore, must be highly collaborative, goal-oriented, flexible, and communicative. An ideal candidate will be responsive, thoughtful, empathetic, initiative-taking, a team player, and able to manage multiple projects effectively and efficiently. This role reports directly to the Clinical Operations Manager.

Duties and Responsibilities:

Clinical Trial Execution:

Exercise judgement within the allowable limits defined within clinical trial protocols, standard operating procedures, and the direction from the study investigator, Operations Manager, and Site Director or Regional Director
Maintain participant privacy and data confidentiality, complying with the appropriate sponsor requirements and regulations, which include the FDA, ICH GCP, HIPAA, institutional review board determinations, and institutional policies and procedures
Complete study-directed assessments with participants, which may include, but are not limited to, informed consent, medical history, adverse events, Fibroscan, memory screen, test article handling, appointment scheduling, records review, treatment coordination, and collecting vital signs
Complete documentation and data management-related tasks as instructed by supervisor and compliance leadership in accordance with GCP and other regulatory guidelines
Function as a liaison with pharmaceutical sponsors and external vendors, including but not limited to, participating in monitoring visits and audits
Responsible for participant management and engagement from the recruitment of study participants to study completion, as applicable.
Respond to internal and external requests for information promptly
Identify opportunities to improve participant care and satisfaction
With a solutions-oriented and collaborative mindset, resolve study-related challenges within a reasonable time set by the supervisor
Establish, develop, and maintain productive relationships with internal and external personnel to achieve a high standard of research outcomes.
Coordinate multiple projects with competing priorities and deadlines as needed, based on clinical trial protocol directives and study volume
Attends the investigator’s meeting, pre-study site visit, study initiation visit, and all other study-related visits hosted by monitors or sponsor representatives as appropriate
Track enrollment status reports to ensure study sites stay on track to meet enrollment goals
Track study-specific status reports to ensure all required information regarding site issues, deviations, and CRF status is kept current

Administration:

Create memos, emails, and letters related to study activities
Create and maintain reports and/or spreadsheets as requested
Assist regulatory personnel in maintaining study documents and ensure electronic regulatory documents are saved and uploaded appropriately
Responsible for reporting safety information to regulatory agencies
Perform quality checks on source documents specific to the study
Assist with the Corrective and Preventive Action Plan (CAPA) process as needed

Duties, responsibilities, and activities may change, or new ones may be assigned at any time.

Education / Experience:

High school diploma or general education degree (GED) required
Bachelor’s Degree in a scientific area of study preferred or equivalent combination of education, training, and experience
1 year of experience as a Clinical Research Assistant or Coordinator
1-2 years of experience in Clinical Research
Proficient in all Microsoft Office applications and Clinical Research IO (CRIO) or equivalent CTMS
Must have strong knowledge of ICH/GCP guidelines
Must complete GCP training before interacting with participants and must recertify every 2 years or as applicable
Trained and certified in the administration of Fibroscan and memory screens as required by the study portfolio and individual experience. Training to be provided
Must have basic life support (BLS) training, provided during onboarding
Demonstrated organizational skills and outstanding time management, including keen attention to detail, with the ability to track multiple projects at one time
Strong written and oral communication skills
Knowledge of basic medical terminology
Possess impeccable integrity and personal and professional values that are consistent with PCR’s high standards and mission
Comply with the company policies, code of ethics, and guiding values always
Proficient in Spanish and English preferred

Supervisory Responsibilities: None

Certificates and Licenses: Valid Driver’s License

Knowledge, Skills, and Other Abilities:

Must be able to effectively communicate with all levels of internal and external contacts
Demonstrated ability to manage a high-volume workload with multiple clinical trials while maintaining accuracy and compliance.
Ability to work independently and multitask in a fast-paced team environment
Strong people skills, including the ability to interact with individuals from diverse backgrounds and to oversee confidential matters and sensitive information with discretion and judgment
Must possess a positive, friendly, and professional demeanor, particularly when interacting with research participants
Must be able to work independently and collaborate with a team
Ability to interpret clinical research protocols
Strong problem-solving and decision-making skills, particularly when under pressure
Proactive at identifying, addressing, and solving issues in real time
Energetic self-starter, results-oriented, and able to work effectively in an entrepreneurial environment

Work Environment and Physical Demands:

The work environment and physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Work is performed in an office/laboratory and/or a clinical environment.
Exposure to biological fluids and/or bloodborne pathogens.
Personal protective equipment is required, such as protective eyewear, garments, and gloves.
Occasional travel may be required, domestic and/or international.
Ability to work in an upright and/or stationary position for 6-10 hours per day.
Frequent mobility required.
Occasional squatting, kneeling, or bending.
Light to moderate lifting and carrying (or otherwise moving) objects, including medical equipment, with a maximum lift of 20-50 lbs.

Benefits of working at Summit Pinnacle Clinical Research:

401k
Medical, dental, vision, long-term disability, short-term disability, FSA, and life insurance
3 weeks of paid time off
14 paid company holidays
Scrub uniform voucher (specific positions apply)
And more!

Summit Clinical Research Solutions is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, disability, gender, national origin, age, genetic information, military or veteran status, sexual orientation, gender identity, marital status, or any other protected Federal, State/Province, or Local status unrelated to the performance of the work involved.

Quick Apply

Refine Your Search

clinical manager jobs in edinburg tx

Clinical Research Coordinator

Clinical Research Coordinator (Contract)

Clinical Nurse Coordinator Emergency Room

Clinical Sales Specialist, Surgical Pain - Houston, TX

Clinical Registered Nurse Coordinator FSED

Clinical Sales Specialist, Interventional Pain - North Texas (DFW, TX)

Clinical Nurse Coordinator Freestanding ED

Clinical Patient Navigator- Medical Office Coordinator

Clinical Behavioral Manager - FT - Days - BH Admin

LVN QI Coordinator -PT Days - Clinical Certification

NPST Clinical Operations Manager

Assistant Clinical Director

Clinical Social Worker

RN Clinical Liaison

Clinical Nurse Coordinator RN Day Surgery

Clinical Nurse Coordinator Special Care Unit

Clinical Donation Coordinator I - PeeDee Region

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