IQVIA
Clinical Research Coordinator, On-Site, Horsham, Pennsylvania
IQVIA, Horsham, Pennsylvania, United States, 19044
Clinical Research Coordinator, On-Site, Horsham, Pennsylvania
Join to apply for the
Clinical Research Coordinator, On-Site, Horsham, Pennsylvania
role at
IQVIA .
Please note this position is fully on-site at the site in Horsham, PA.
Join a collaborative, patient-centered team where your contributions directly support groundbreaking studies and improved patient outcomes. This is more than just a CRC role – it’s a unique opportunity to deepen your expertise in clinical trial coordination, grow within a supportive environment that values professional development, and make real progress toward your career goals. It’s an ideal fit for a hardworking, driven, and passionate individual who thrives in a fast‑paced, team‑oriented setting and is eager to make a meaningful impact through clinical research.
Overview Coordinate and participate in clinical research studies ensuring that studies are carried out according to protocol, contracted scope of work, good clinical practice, sponsor and Avacare standard operating procedures (SOPs) and any relevant local guidelines and regulations.
Essential Functions
Coordinate clinical research studies conducted by a supervising principal investigator.
Assist as backup CRC on other studies.
Develop and implement patient recruitment strategies; actively recruit to ensure enrollment targets are achieved.
Obtain informed consent of research subjects.
Develop strong working relationships and maintain effective communication with study team members.
Complete all protocol related training.
Perform patient/research participant scheduling.
Collect patient/research participant history.
Collect and maintain source documentation.
Manage inventory and administer test articles/investigational product to participants.
Perform data entry and query resolution.
Support the collection and review of required essential study documents and reports. Order supportive study supplies (e.g., contracts, IXRS, lab kits, nonclinical supply materials, imaging, and laboratory handling manuals).
Adhere to an IRB approved protocol.
Support the safety of research subjects, report adverse events.
Coordinate protocol related research procedures, study visits, and follow‑up.
Facilitate pre‑study, site qualification, study initiation, monitoring visits, and study close‑out activities.
Collect, process and ship laboratory specimens.
May be asked to perform special project responsibilities and travel to other clinic locations, within the area, when needed.
Comply with Avacare and Sponsor policies, standard operating procedures (SOPs) and guidelines.
Perform other duties as assigned.
Qualifications
Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines.
Clinical Research Coordinator experience within a similar setting.
Clinical skills experience including obtaining vitals, phlebotomy, EKG, etc.
Knowledge and experience of site operations and the drug development process.
Effective communication.
Computer proficiency in use of Microsoft Word, Excel.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
Seniority Level:
Entry Level
Employment Type:
Full‑time
Job Function:
Research, Analyst, and Information Technology
Industries:
Hospitals and Health Care
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law.
The potential base pay range for this role, when annualized, is $36,600.00 – $91,300.00. The actual base pay offered may vary based on a number of factors including job‑related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part‑time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
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Clinical Research Coordinator, On-Site, Horsham, Pennsylvania
role at
IQVIA .
Please note this position is fully on-site at the site in Horsham, PA.
Join a collaborative, patient-centered team where your contributions directly support groundbreaking studies and improved patient outcomes. This is more than just a CRC role – it’s a unique opportunity to deepen your expertise in clinical trial coordination, grow within a supportive environment that values professional development, and make real progress toward your career goals. It’s an ideal fit for a hardworking, driven, and passionate individual who thrives in a fast‑paced, team‑oriented setting and is eager to make a meaningful impact through clinical research.
Overview Coordinate and participate in clinical research studies ensuring that studies are carried out according to protocol, contracted scope of work, good clinical practice, sponsor and Avacare standard operating procedures (SOPs) and any relevant local guidelines and regulations.
Essential Functions
Coordinate clinical research studies conducted by a supervising principal investigator.
Assist as backup CRC on other studies.
Develop and implement patient recruitment strategies; actively recruit to ensure enrollment targets are achieved.
Obtain informed consent of research subjects.
Develop strong working relationships and maintain effective communication with study team members.
Complete all protocol related training.
Perform patient/research participant scheduling.
Collect patient/research participant history.
Collect and maintain source documentation.
Manage inventory and administer test articles/investigational product to participants.
Perform data entry and query resolution.
Support the collection and review of required essential study documents and reports. Order supportive study supplies (e.g., contracts, IXRS, lab kits, nonclinical supply materials, imaging, and laboratory handling manuals).
Adhere to an IRB approved protocol.
Support the safety of research subjects, report adverse events.
Coordinate protocol related research procedures, study visits, and follow‑up.
Facilitate pre‑study, site qualification, study initiation, monitoring visits, and study close‑out activities.
Collect, process and ship laboratory specimens.
May be asked to perform special project responsibilities and travel to other clinic locations, within the area, when needed.
Comply with Avacare and Sponsor policies, standard operating procedures (SOPs) and guidelines.
Perform other duties as assigned.
Qualifications
Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines.
Clinical Research Coordinator experience within a similar setting.
Clinical skills experience including obtaining vitals, phlebotomy, EKG, etc.
Knowledge and experience of site operations and the drug development process.
Effective communication.
Computer proficiency in use of Microsoft Word, Excel.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
Seniority Level:
Entry Level
Employment Type:
Full‑time
Job Function:
Research, Analyst, and Information Technology
Industries:
Hospitals and Health Care
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law.
The potential base pay range for this role, when annualized, is $36,600.00 – $91,300.00. The actual base pay offered may vary based on a number of factors including job‑related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part‑time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
#J-18808-Ljbffr