20 Best Study Manager jobs (Hiring Now!)

Clinical Research Coordinator
CenExel Rocky Mountain Clinical Research —Englewood, CO
CCRC certification not required, but preferred. O Responsible for timely data entry and query resolution. Knowledge of all components of the research process as…
$29 - $32 an hour
Quick Apply
Clinical Research Coordinator (CRC)-FT
Evolution Research Group —Columbus, OH
Manage studies with Principal Investigator, Site Director, and Recruitment Manager to develop effective programs for study enrollment.
Estimated: $49.3K - $62.4K a year
Quick Apply
Clinical Research Coordinator
Alliance for Multispecialty Research, LLC —Fort Myers, FL
Advise Investigator, Sub-Investigator and staff on protocols, procedures required for the successful implementation and completion of each clinical research…
From $25 an hour
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3d
Clinical Research Coordinator
Alliance for Multispeciality Research —New Orleans, LA
Attach original document to certified copy before filing in the patient’s chart. Advise Investigator, Sub-Investigator and staff on protocols, procedures…
$24 - $27 an hour
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12d
Senior Clinical Research Coordinator
Evolution Research Group —Staten Island, NY
Manage studies with Principal Investigator, Site Director, and Recruitment Manager to develop effective programs for study enrollment.
$30 - $38 an hour
Quick Apply
12d
Clinical Study Manager (USA - REMOTE)
VivoSense Inc —Boston, MA
This is a multi-faceted role in which you will have the opportunity to lead the scientific offering on client projects including 1) driving all phases of…
$90,000 - $120,000 a year
Quick Apply
16h
Clinical Research Site Manager
Alliance for Multispeciality Research, LLC —Layton, UT
Hire, train and develop new team members to meet organizational needs. Provide timely feedback on employee performance, helping to develop a team members skill…
$90,000 - $95,000 a year
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4d
Senior Clinical Data Manager
Celldex Therapeutics, Inc. —New Haven, CT
Initiate CRF development for new clinical trials and protocol amendments; collaborate with internal team and responsible vendor on CRF development, database…
Estimated: $124K - $157K a year
Clinical Research Coordinator I Registered Nurse
Novant Health —Charlotte, NC
Licensure/Certification: Current RN licensure in appropriate state, required. Additional Skills (preferred): Good Clinical Practice (GCP), Human Subjects…
Estimated: $57K - $72.2K a year
7d
Regulatory Study Start-Up Specialist
Care Access —Remote
The Regulatory Study Start-Up Specialist will oversee all details of regulatory for assigned trials for both the traditional and decentralized site models and…
Estimated: $64.1K - $81.2K a year
Quick Apply
4d
Remote Clinical Trial Manager
Medilink Therapeutics —Remote
Coordinates the development and distribution of critical study documents, including ICFs, operational documents, study reference documents, study newsletters,…
$125,000 - $145,000 a year
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Clinical Project Manager
Technical Resources International, Inc. —Bethesda, MD
Broad multidisciplinary understanding of the pharmaceutical clinical research and development processes with hands on regulatory, clinical operations, or…
Estimated: $106K - $134K a year
Remote Clinical Data Manager
Redbock- an NES Fircroft company —Remote
CLINICAL DATA MANAGER- Part time remote contract position*. 5+ years of Clinical Data experience. Must be strong with excel-will be using daily.
$50 - $60 an hour
Quick Apply
Non-Clinical Study Manager
Astellas —South San Francisco, CA
Understanding of gene therapy and/or novel biologics concepts and methodologies, in particular as they relate to nonclinical study design and data analysis.
$114,800 - $153,000 a year
3h
Clinical Research Nurse Coordinator
University of Alabama at Birmingham —Birmingham, AL
Bachelor's degree in a related field and three (3) years of related experience required. May provide oversight to junior clinical research coordinators (CRC)…
Estimated: $54.2K - $68.6K a year
Clinical Research Coordinator/Medical Assistant
Alliance for Multispecialty Research, LLC —Layton, UT
Advise Investigator, Sub-Investigator and staff on protocols, procedures required for the successful implementation and completion of each clinical research…
$20 - $23 an hour
Quick Apply
4d
Clinical Research Coordinator (medical research trial coordinator with 1 year experience)
One of a Kind Clinical Research Center CA LLC —Napa, CA
Data collection, entry, query resolution. Our site is responsible for coordinating a clinical trial start up, participant recruitment, trial management and…
$23 - $25 an hour
Quick Apply
Medical Assistant/Clinical Research Coordinator
Alliance for Multispecialty Research, LLC —Wichita, KS
Advise Investigator, Sub-Investigator and staff on protocols, procedures required for the successful implementation and completion of each clinical research…
$24 an hour
Quick Apply
Study Coordinator
Albert Einstein College of Medicine —Bronx, NY
Arrange meetings of study partners, develop meeting agendas, and facilitate meeting; Work with Principal Investigator to refine and finalize research protocols,…
$30 an hour
Study Coordinator
University of North Carolina at Chapel Hill —Chapel Hill, NC
The position will have the primary responsibility for carrying out study related procedures accurately, for monitoring the safety and well-being of study…
$53,772 - $68,000 a year
4d

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Clinical Research Coordinator

CenExel Rocky Mountain Clinical Research - Englewood, CO

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Job Details

Full-time $29 - $32 an hour

Benefits

Health savings account
Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance
401(k) matching
Employee discount
Flexible schedule
Life insurance

Qualifications

Microsoft Word
CCRC
Microsoft Excel
Clinical research
Phlebotomy
Clinical trials
Good Clinical Practice
Computer skills
Neurology
1 year
Care plans

Full Job Description

About Us:

Each of CenExel’s research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.

Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.

Job Summary:

Responsible for coordinating all aspects of clinical trials with the strictest adherence to ICH, GCP, protocol, and company guidelines, regulations, and policies.

Essential Responsibilities and Duties:

· Coordinating all aspects of patient involvement from study initiation until study completion;

· Study start-up:

· o assist in the creation of thorough and accurate source documents;

· o Work collaboratively with other internal departments, sponsors and investigators to ensure protocols are understood and assist in the trainings of staff members

· o Participate in IMs and SIVs; communicating with sponsors and representatives

· o Ensure site receives accurate information and supplies from sponsors (i.e.: source, protocol, scales, supplies, approvals, contacts, etc.)

· Screening participants for actively enrolling studies

· o Assist in reviewing all participant history from Pre-Enrollment and Enrollment departments confirming information with potential participant and study physician

· o Educating potential participants and caregivers on protocol specific details and expectations;

· o Working with the physician to address all questions and concerns related to the trial and informed consent process;

· o Maintaining thorough knowledge of study specific inclusion/exclusion criteria

· Coordinating scheduled visits and adhering to protocol visit windows and timelines

· o Perform or follow up on safety and efficacy assessments per protocol  vital signs, EKGs, blood draws and other assessments as assigned

· o Collaborating with the research pharmacist to perform drug accountability and compliance at each visit and educating subject on proper dosing regimen

· o Accurate and timely completion of source documents recording subject’s participation in study

· o Communicate closely with all departments to ensure study visits are coordinated in compliance with protocol and GCP guidelines

· o Assist investigators in collection of information from study subjects regarding AEs, concomitant medications and other changes throughout participation

· o Responsible for subject scheduling, in coordination with Recruiting

· o Responsible for timely data entry and query resolution

· o Timely reporting of study events (SAEs, protocol deviations, etc) to appropriate departments and other outside agencies (Sponsors, CRO’s, etc.)

· o Following subjects through study completion and creating follow-up care plan with physician, study subject and primary care provider;

· Ensuring preparation for and facilitating of all study monitoring visits and following up promptly with monitor follow-up letters

· Prompt and professional communication with sponsors, representatives and other study related parties

· Maintaining professional and appropriate interactions with study subjects, caregivers, sponsors and all other study related personnel, and staff members

· Keeping management informed of study status and any study-related issues

· Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.

Education/Experience/Skills:

At least 1 years of experience working as a Clinical Research Coordinator.
CCRC certification not required, but preferred
Experience in neurology not required, but preferred
Knowledge of “good clinical practices” for clinical research as defined by the Code of Federal Regulations (CFR).
Demonstrate organizational skills to efficiently and effectively manage multiple clinical trials while providing accurate information in a timely manner.
Communicate and work effectively with a diverse team of professionals
Phlebotomy and ECGs experience not required, but preferred
Knowledge of all components of the research process as it pertains to clinical trials and studies, i.e., IRB procedures and processes, data management, etc.
Demonstrated interpersonal skills to work with physicians, administrators, work colleagues, representatives from sponsors and others to achieve maximum efficiency in reaching and maintaining workplace goals in a professional manner.
Must be self-directed and be able to manage multiple projects and responsibilities.
Computer skills using PC platform computers with proficiency in Excel and Word to enter data and generate correspondence accurately and experience with various EDC platforms
Experience with IRB portals, such as WIRB and Advarra preferred
A critical thinker with strong attention to detail and superb problem-solving abilities.

Compensation: $28-32/h.

Application window will close on June 25th, 2024.

Working Conditions

Indoor, office environment.
Essential physical requirements include sitting, typing, standing, and walking.
Lightly active position, occasional lifting of up to 20 pounds.
Reporting to work, as scheduled, is essential.

CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.

Job Type: Full-time

Pay: $29.00 - $32.00 per hour

Benefits:

401(k) matching
Dental insurance
Employee discount
Flexible schedule
Health insurance
Health savings account
Life insurance
Paid time off
Vision insurance

Experience:

Clinical research: 1 year (Required)
randomizing patients: 1 year (Required)
conducting patients visits: 1 year (Required)

Ability to Commute:

Englewood, CO 80113 (Required)

Work Location: In person

Quick Apply

Study Manager jobs

Clinical Research Coordinator

Clinical Research Coordinator (CRC)-FT

Clinical Research Coordinator

Clinical Research Coordinator

Senior Clinical Research Coordinator

Clinical Study Manager (USA - REMOTE)

Clinical Research Site Manager

Senior Clinical Data Manager

Clinical Research Coordinator I Registered Nurse

Regulatory Study Start-Up Specialist

Remote Clinical Trial Manager

Clinical Project Manager

Remote Clinical Data Manager

Non-Clinical Study Manager

Clinical Research Nurse Coordinator

Clinical Research Coordinator/Medical Assistant

Clinical Research Coordinator (medical research trial coordinator with 1 year experience)

Medical Assistant/Clinical Research Coordinator

Study Coordinator

Study Coordinator

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