Clinical Trial Participant Recruitment Manager Task
4 days ago
**Overall Purpose of the Position**:
The Clinical Trial Participant Recruitment Manager is responsible for overseeing the recruitment of participants for clinical research studies. The role involves managing a team of recruiters, developing, implementing, and managing strategies to recruit and retain participants for clinical trials. This role ensures recruitment targets are met while adhering to regulatory standards, ethical guidelines, and study protocols. The manager works closely with clinical teams, sponsors, community engagement teams and other relevant external stakeholders to optimize recruitment processes, improve participant diversity, and ensure high-quality data collection.
**Key Performance Areas (KPAs) & Responsibilities include, but not limited to**:
**Recruitment Strategy Development**
- Developing recruitment plans tailored to specific clinical trials, aligned with target demographics, study requirements, and timelines.
- Collaborating with study coordinators and principal investigators to understand study requirements and target populations.
- Utilising data analytics and market research to identify effective recruitment channels and strategies.
**Participant Outreach and Engagement**
- Developing and managing outreach campaigns using digital platforms, community engagement, and healthcare networks.
- Fostering, building and maintaining relationships with patient advocacy groups, community organisations, and healthcare providers to promote trial awareness.
**Team Management and Collaboration**
- Leading, mentoring and managing recruitment teams, including coordinators and outreach specialists, ensuring clear communication and goal alignment.
- Collaborating with clinical investigators, study sponsors, CROs and other relevant stakeholders to align recruitment efforts with study objectives.
**Operational Management**
- Overseeing the day-to-day operations of the recruitment team to ensure smooth and efficient processes.
- Monitoring recruitment metrics and key performance indicators (KPIs) to assess the effectiveness of recruitment strategies and implement improvements as needed.
- Ensuring that recruitment activities are conducted in accordance with regulatory requirements and ethical guidelines.
- Fostering a culture of accountability and transparency within the recruitment team.
**Regulatory and Ethical Compliance**
- Ensuring all recruitment activities comply with SA GCP (Good Clinical Practice), Ethical and other relevant regulatory standards.
- Overseeing the creation of participant-facing materials to ensure ethical, clear, and culturally sensitive communication.
**Monitoring, Reporting and Communication**
- Tracking recruitment and other relevant metrics, including enrolment rates, participant retention, and diversity statistics.
- Providing status updates to team leads in a regular and relevant manner
- Communicating efficiently with all stakeholders
- Preparing detailed reports on recruitment progress for internal stakeholders and sponsors.
**Innovation and Process Improvement**
- Exploring and implementing innovative recruitment methods, such as leveraging social media campaigns, mobile technology, and AI-driven tools.
- Continuously evaluating the effectiveness of recruitment strategies and refine processes to enhance efficiency and participant experience
**Ideal Requirements**
- Bachelor’s degree in Life Sciences, Public Health, Marketing, or related field
- At least 2 years of experience in clinical trial recruitment, healthcare marketing, or patient engagement (preferred)
- Proven track record of meeting recruitment goals for diverse populations or similar experience.
- Experience in team supervision / management and leadership
- Proficiency in the use of clinical trial management systems (CTMS) or similar tools
- Familiarity with digital marketing tools.
**Key Personal Inherent Characteristics**
- Effective communication and interpersonal skills.
- Ability to work collaboratively across diverse teams and with external stakeholders.
- Problem-solving and decision-making abilities under time-sensitive conditions.
- Strong organisational skills, with the ability to oversee multiple tasks, projects, and team members
- Adaptability in recruitment strategy implementation
- Commitment to ethical recruiting practices and inclusivity in participant engagement
- Results-oriented, proactive, and self-motivated with a focus on driving success in clinical trial recruitment
**Details**:
**Area**:Parow, Cape Town
**Contract Type**: Permanent
**Applications Close**:16 December 2024
TASK reserves the right to withdraw this advertisement and not fill the above-mentioned vacancy at any stage during the recruitment process.
Meeting our employment equity goals will be acknowledged during the recruitment process.
**About the Company**:
TASK is a South African headquartered, multinational clinical research institute that conducts clinical trials to determine the treatment effects o
-
Senior Clinical Trial Recruitment Manager
1 week ago
Cape Town, South Africa TASK Full time**About the Company**: TASK is a South African headquartered, multinational clinical research institute that conducts clinical trials to determine the treatment effects of novel medicinal products or devices in healthcare and offers services in conducting complex clinical trials in a wide variety of therapeutic areas. **Overall Purpose of the...
-
Clinical Trial Recruiter
7 hours ago
Cape Town, South Africa TASK Full time**Overall Purpose of the Position**: The Clinical Trial Recruiter (Nurse) will be responsible for supporting the recruitment of participants for various clinical trials conducted across TASK’s Cape Town sites. This role involves establishing new relationships, identifying recruitment opportunities, and executing recruitment strategies in collaboration with...
-
Cape Town, South Africa TASK Full time**Overall Purpose of the Position**: The Clinical Trial Assistant I (CTA I) plays a crucial role in supporting the efficient operation of clinical research activities by providing comprehensive administrative and data management assistance. The Clinical Trial Assistant I ensures the smooth execution of daily study tasks, maintains accurate study...
-
Research Nurse Task Clinical Research Centre
7 hours ago
Cape Town, South Africa TASK Full time**Overall Purpose of the Position**: The purpose of this role is to perform procedures following the visit schedule as stipulated in each protocol and monitor the health and safety of the participants, and document the response to an intervention, which is typically new drug or therapy in the source documents. The Research Nurse (RN) will be responsible for...
-
Research Nurse Task Clinical Research Centre
2 weeks ago
Cape Town, South Africa TASK Full time**About the Company**: TASK is a South African headquartered, multinational clinical research institute that conducts clinical trials to determine the treatment effects of novel medicinal products or devices in healthcare and offers services in conducting complex clinical trials in a wide variety of therapeutic areas. **Overall Purpose of the...
-
Research Physician
4 days ago
Cape Town, South Africa TASK Full time**Overall Purpose of the Position**: To fulfil the role of Sub-Investigator or Principal Investigator in oncology-focused clinical trials, assessing the safety and efficacy of novel cancer treatments or diagnostic options while upholding strict ethical and scientific standards. **Key Performance Areas (KPAs) & Responsibilities include, but not limited...
-
Study Coordinator Task Brooklyn
2 weeks ago
Cape Town, South Africa TASK Full time**Overall Purpose of the Position**: A study coordinator plays a pivotal role in the execution and management of clinical trials conducted at the research site. The position needs to acquire in-depth knowledge of relevant study protocols and will be responsible for coordinating various aspects of the clinical trial process to ensure compliance with...
-
Impactful Clinical Trials Coordinator
2 weeks ago
Cape Town, South Africa Task Applied Science Full timeA clinical research institute is seeking a study coordinator in Cape Town. The role involves managing clinical trials, ensuring compliance with regulatory standards, and coordinating participant recruitment. The ideal candidate will have a nursing qualification and experience in clinical trials. Strong organizational and communication skills are essential....
-
Clinical Trial Administrator
4 days ago
Cape Town, South Africa TASK Full time**Overall Purpose of the Position**: As a highly organised and detailed-oriented individual, the Clinical Trial Administrator will be responsible for managing the processing and handling of clinical research samples in compliance with relevant policies, procedures and regulatory standards. The role involves coordinating the receiving, processing, storing and...
-
Research Nurse Task Brooklyn
4 days ago
Cape Town, South Africa TASK Full time**Overall Purpose of the Position**: The purpose of this role is to perform procedures following the visit schedule as stipulated in each protocol and monitor the health and safety of the participants, and document the response to an intervention, which is typically new drug or therapy in the source documents. The Research Nurse (RN) ensures that the...