Human Resources Specialist

Location : New Haven, CT

Benefits : At Invicro you will be learning, challenging yourself, and having fun while collaborating with teammates through the open exchange of ideas.

Our outstanding benefits program includes medical, dental, vision, 401k with a 4% employer match, FSA, paid sick leave, and generous paid time off (PTO) program.

You can learn more about the benefits here.

Overview :

The Clinical Research Coordinator is responsible for coordinating and administering research study associated activities.

Assists in project planning. Ensures the smooth and efficient day-to-day operation of research and data collection activities.

This position requires frequent close interactions with participants, physicians and other staff members. Complete, accurate and timely reporting of data is essential.

Essential Job Functions :

• Participates in clinical research studies from study initiation through close-out and archiving.
• Under the direction of the Principal Investigator, undertakes all essential, operational and patient care responsibilities associated with day-to-day clinical trial and study visit activities following good clinical practice guidelines.
• Recruits, screens and enrolls subjects according to specific protocol requirements
• Works closely with the protocol and completes the consenting process, along with reviewing inclusion / exclusion criteria to determine eligibility of study participants.
• Develops, maintains and version controls source documents and tracking logs relevant to the study.
• Completes study visit activities including EKGs, phlebotomy, taking vital signs, laboratory sample processing and shipment.
• Conducts adverse event information collection, concomitant medication review, and neuropsychological scales.
• Manages study monitoring visits; completes the study Case Report Form (CRF).
• Ensures diagnostic specimens are packaged per IATA (International Air Transport Association) guidelines.
• Abides by Good Clinical Practices (GCP) and complies with all company Standard Operating Procedures (SOP).
• Assists with IRB and Regulatory submissions.

Required Qualifications

• Bachelor’s Degree in a science or relevant field.
• 1-5+ years of relevant experience.
• Knowledge of Good Clinical Practices (GCP) and other Regulations.
• Must be detail oriented, organized, and able to multitask in fast paced environment.
• Excellent communication, interpersonal and facilitation skills.
• Ability to work collaboratively with other members of the clinical research team and other sites.
• Computer competency including proficiency in Microsoft Word, Excel and PowerPoint.
• Ability to perform EKGs, vital signs, and phlebotomy.
• Understanding Phases I-IV drug development process.

Position Specifics :

• Monday - Friday
• Infrequent Weekend and Holiday Work
• Not a remote position

What We Offer :

• Competitive salary
• Full Benefits
• 401k with generous matching
• Flexible vacation policy

Invicro is an Equal Opportunity Employer. We maintain a drug-free work environment. All qualified applicants will receive consideration for employment without regard to actual or perceived race (and traits historically associated with race, including, but not limited to hair texture and protective hairstyles such as braids, locks, and twists), color, creed, religion, citizenship status, sex or gender (including pregnancy, childbirth and related medical conditions), parental status, sexual orientation, gender identity, gender expression (including transgender status), national origin, ancestry, age, marital status or protected veteran status and will not be discriminated against on the basis of physical or mental disability, protected medical condition as defined by applicable state or local law, genetic information, political affiliation or any other characteristic protected by applicable federal, state, or local laws and ordinances.

Invicro does not accept unsolicited resumes from individual recruiters, third party recruiting agencies, outside recruiters or firms without an executed contract in place.

We are not responsible for any fees related to resumes that are unsolicited or are received by Invicro. Such resumes will be deemed the sole property of Invicro and will be processed accordingly.