Patient Recruitment Manager (Clinical Research)

CBH Health

$70K — $95K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Fluent in English and Spanish, both written and verbal.
  • Bachelor's Degree or equivalent experience preferred.
  • Knowledge of clinical sponsor requirements and participant evaluation processes.
  • Understanding of clinical protocols from Phase I to Phase IV.
  • Strong organizational and record maintenance skills.
  • Ability to work independently and as part of a team.
  • Capable of managing multiple projects with a flexible approach.

Responsibilities

  • Develop recruitment programs to enhance clinical trial participation.
  • Act as a liaison with referral sources and new staff training.
  • Identify and implement strategies for improving patient enrollment.
  • Supervise Recruitment Specialists and overall recruitment operations.
  • Evaluate and optimize the enrollment process for studies.
  • Conduct outreach and organize special events for referral connections.
  • Champion adherence to compliance and best practices in recruitment.

Benefits

  • Supportive work environment with opportunities for professional development.
  • Gain experience in managing and training a team.
  • Exposure to a wide range of clinical research protocols.
  • Potential for flexible task management in a dynamic setting.
Full Job Description
Job Summary:

The Patient Recruitment Manager will be responsible for creating programs and solutions to support clinical trial recruitment and retention.

Essential Responsibilities and Duties:
  • Communicates and reaches out to referral connections, sponsors, or potential providers.
  • Acts as the liaison for outside referring sources.
  • Trains new staff members in the department.
  • Identifies strategies to improve patient enrollment in research protocols in collaboration with Principal Investigator and/or site leadership.
  • Supervises Recruitment Specialists and oversees recruitment department.
  • Determines study support required for trials and understand enrollment needs and timelines of trials.
  • Develops pre-screen scripts for new studies.
  • Evaluates enrollment process to ascertain if current process recruits optimal study participant population.
  • Conducts outreach and special events as needed and conducts presentations to various referral sources.
  • Hires, trains, supervises, and evaluates personnel. Champions and enforces the strictest adherence to best practices, FDA Code of Federal Regulations, ICH (International Conference on Harmonization), GCP (Good Clinical Practices), CenExel standard operating procedures, site Working Practices, protocol, and company guidelines and policies. Retrains and implements corrective and preventative actions, as needed.
  • 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:
  • Must be able to effectively communicate verbally and in writing in both English and Spanish.
  • Bachelor's Degree or equivalent experience preferred.
  • Knowledge of sponsors/study requirements and participant evaluation procedures.
  • Understanding of clinical protocols Phase I to Phase IV.
  • Skill in organization and record maintenance.
  • Ability to work independently as well as functioning as part of a team.
  • Must be self-directed and able to work with minimal supervision.
  • Able to take a flexible approach to shifting priorities.
  • Able to manage multiple projects and responsibilities.
  • Motivated to work consistently in a fast paced and rapidly changing environment.


Working Conditions
  1. Indoor, Office environment.
  2. Essential physical requirements include sitting, typing, standing, and walking.
  3. Lightly active position, occasional lifting of up to 20 pounds.
  4. Reporting to work, as scheduled, is essential.
  5. On site work arrangement.

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