Top 7 Clinical research associate Jobs in Williamsburg Va

Clinical Research Coordinator I
TIDEWATER PHYSICIANS MULTISPECIALTY GROUP P C —Newport News, VA
- From $52,243 a year
- Full-time
- Ability to walk for extended periods
- Word processing
- HIPAA
RN Oncology Clinical Research Coordinator
Riverside Hospital Services —Gloucester, VA
- $68,000 - $93,500 a year
- Full-time
- Nursing
- Patient monitoring
- RN License
Quick Apply

More jobs to discover

Find similar jobs that you might be interested in.

RN Oncology Clinical Research Coordinator
Riverside Hospital Services —Gloucester, VA
Performs duties related to the conduct of clinical trials in accordance with RHS policies, protocol requirements as well as all local, state, and federal…
$68,000 - $93,500 a year
Quick Apply
Clinical Research Nurse/Coordinator
Virginia Oncology Associates —Norfolk, VA
Current BCLS or ACLS certification required. OCN, SoCRA, or ACRP certification preferred. Experience with computer data entry and database management.
$47,964.80 - $128,939.20 a year

Show more similar jobs

Explore jobs in cities nearby

Check out jobs in cities near your current location, Columbus

Clinical Research Assistant - Oncology
The Ohio State University Wexner Medical Center —Columbus, OH
Bachelor's degree in biological sciences, health sciences, social sciences, or other related field, or an equivalent combination of education & experience…
12d
Lab Services Coordinator - Clinical Trials Processing Lab
The Ohio State University Wexner Medical Center —Columbus, OH
Participates in data entry and management, quality control, audits and FDA inspections, continuous quality improvement and inventory management of clinical…
12d

Show more jobs in cities nearby

I want to receive the latest job alert for clinical research associate in williamsburg va

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

clinical research associate jobs near williamsburg va

Clinical Research Coordinator jobs in Newport News, VA

Clinical Research jobs in Reno, NV

Clinical Nurse Coordinator jobs in East Grand Forks, MN

Clinical Nurse Coordinator jobs in Baton Rouge, LA

Clinical Psychologist jobs in Austin, TX

Clinical Nurse Coordinator jobs in Columbus, OH

Nurse Practitioner jobs in Lafayette, IN

Clinical Nurse Coordinator jobs in Racine, WI

Mds Coordinator jobs in Cherry Hill, NJ

Clinical Research Coordinator jobs in Minneapolis, MN

Clinical Nurse Instructor jobs in Collin County, TX

Clinical Research Coordinator jobs in Santa Monica, CA

Clinical Research Coordinator jobs in Irvine, CA

Supply Chain Coordinator jobs in New Jersey

Patient Care Coordinator jobs in Chicago, IL

Clinical Research Coordinator jobs in San Francisco, CA

Clinical Research Coordinator I

TIDEWATER PHYSICIANS MULTISPECIALTY GROUP P C -
Newport News, VA

Apply Now

Job Details

Full-time
From $52,243 a year

Qualifications

Driver's License

Full Job Description

Position Summary

The Clinical Research Coordinator I conduct high quality clinical research following the highest ethical and regulatory standards of care.

Major Duties and Responsibilities

Become familiar with the design of proposed and implemented studies.
Review study protocols to evaluate factors such as sample collection processes, data management plans, and potential risks to subject patients.
Communicate well with patients, medical personnel, research sponsors, and institutional review boards (IRBs).
Assess eligibility of potential subjects through screening interviews, review of medical records, and discussion of patient status with physicians and nurses.
Inform patients and caregivers of study designs, risks, and outcomes to be expected.
Organize sites for study equipment and supplies.
Contact industry representatives to ensure that the equipment and software specifications needed for successful study completion are available.
Attend meetings required by research sponsors; some travel and overnight stays may be required.
Enroll patients in clinical studies, ensuring that informed consent is obtained and documented in accordance with all applicable regulatory and ethical requirements at the federal, state, and local levels.
Schedule subjects for appointments, procedures, or inpatient stays as required by study protocols.
Order the drugs and/or devices necessary for studies.
Dispense medication and/or medical devices, calculate dosages, and provide instruction for patients as necessary.
Comfortable handling lab specimens which may include blood, urine, vaginal fluids, joint aspirants, sputum or others.
Competent in the processing, labeling specimen tubes, filling out requisitions, working with dry ice, storing and shipping lab specimens as required.
Collect and maintain study data, which may be either electronic and/or printed, depending on the study.
Obtain subject follow-up information and communicate with health care providers and subjects as necessary.
Register protocol patients with appropriate statistical centers as required.
Prepare and maintain records of study activities, including case report forms, drug dispensation records, and regulatory compliance.
Prepare and maintain study-related protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, and progress reports.
Record adverse events and side effect data and confer with investigators regarding the reporting of events to oversight agencies.
Collaborate with investigators to prepare reports and presentations concerning clinical study procedures, results, and conclusions.
Track enrollment status of subjects, document causes of dropout, and document efforts to contact subjects.
Become familiar with relevant electronic medical records and HIPAA law.
Monitor studies to ensure compliance with protocol design.
Monitor studies to ensure compliance with federal, state and local regulations and TPMG's ethical policies.
Prepare for and participate in audits conducted by study sponsors, federal agencies, and specifically designated review groups.
Maintain contact with sponsors to schedule and coordinate site visits and answer questions about all issues with records or data
Identify protocol problems, inform investigators of problems, and assist resolution of such problems
Confer with health care professionals to determine the best recruitment practices for studies.
Develop advertising and other informational materials to be used in subject recruitment.
Meet with physician groups as needed.
Participate in preparation and management of research budgets.
Participate in the billing process for studies and oversee monetary disbursements.
Participate in training and quality assurance programs.
Review scientific literature, participate in continuing education activities, or attend conferences and seminars to maintain current knowledge of clinical study affairs and issues.
Ability to work well independently and with a team.
Ability to refocus attention easily after multiple interruptions.
Ability to remain organized despite multiple paper charts being utilized at the same time.
Using your own transportation to purchase dry ice for laboratory specimen shipments and taking the packages to USPS, UPS, and or FedEx for delivery as needed.
Willing to perform work related tasks off-site when necessary.
Willing and eager to learn new things.
Other duties as assigned.

Compensation starts at $52,243 per year, with the final annual salary determined by the candidate's relevant experience and qualifications.

Knowledge, Skills and Abilities

Knowledge of appropriate medical terminology.
Knowledge of appropriate email etiquette and effective communication.
Knowledge of clinical study affairs and issues.
Ability to work scheduled hours as defined in the job offer and to use time effectively.
Ability to determine appropriate course of action in more complex situations.
Ability to present information to top management, public groups, and/or boards of directors effectively.
Ability to define problems, collect data, establish facts, and draw valid conclusions.
Ability to manage multiple and simultaneous responsibilities.
Ability to read and understand oral and written instructions and follow written protocols.
Ability to manage data, prepare spread sheets, and apply mathematical concepts such as probability, statistical inference, and basic concepts of algebra and geometry to practical situations.

Education / Training / Requirements

Bachelor’s degree from a four-year college or university, one to two years related experience and/or training, or equivalent combination of education and experience.
Patient care experience is highly desired.
Legible handwriting is a requirement.
Phlebotomy experience desired but not required.
GCP certification, IATA certification desired but not required for consideration.
Current driver’s license and reliable vehicle
Certification by the Association of Clinical Research Professionals (ACRP) or similar organization is preferred but not required.
Ability to learn new tasks and apply skills and knowledge to various work activities.

Physical Demands

Ability to stand and walk for long periods of time.
Ability to sit for extended periods of time.
Ability to climb or balance for limited periods of time.
Ability to occasionally reach, bend, stoop and lift up to 50 lbs. *
Ability to grasp and hold up to 25 lbs.*
Ability to hear normal voice level communications in person or through the telephone.
Ability to speak clearly and understandably.
Ability to taste and smell.
Ability to look at a computer screen for many hours of the day.

Success Factors

Alignment with Company Mission and Core Values
Excellent Time Management/Organized
Open Communication/Positive
Goal Driven
Excellent Customer Service
Juggles Multiple Priorities
Accuracy and Attention to Detail
Accomplished in word processing and worksheet utilization

All statements are essential functions of the position unless identified as non-essential by an asterisk (*).

Apply Now

Refine Your Search

clinical research associate jobs in williamsburg va

Clinical Research Coordinator I

RN Oncology Clinical Research Coordinator

More jobs to discover

Explore jobs in cities nearby

I want to receive the latest job alert for clinical research associate in williamsburg va

Explore jobs in more locations

Job Seeker Tools

Employer Tools

Browse

Stay Connected