CRA/Sr CRA Early Development Services

Job description

PPD’s mission is to improve health.

It starts as an idea to find a cure.

It becomes a life saved.

All in-between, it’s you! We know that meaningful results not only require the right approach, but also the right people.

We invite you to re-imagine health promoting protocols with us, working alongside our talented, bright and energetic teams.



Our global Early Development Services (EDS) is focused on Phase I trials which are designed to assess the safety (pharmacovigilance), tolerability, pharmacokinetics, and pharmacodynamics of an investigational drug or biologic.

Across a number of therapeutic areas, we specialize in the monitoring of these study designs: First in Human, Single Ascending Dose (SAD), Multiple Ascending Dose (MAD), Food Effect (FE), Drug-Drug Interaction (DDI), Bioavailability, Bioequivalence, ADME, Ethnic Bridging, Renal Impairment, and Hepatic Impairment.



At PPD we hire the best, develop ourselves and each other, and recognize the power of being one team.

We offer continued career advancement opportunities, award winning training and benefits focused on the health and wellbeing of our employees.

Summarized Purpose:

As an EDS CRA you will be part of designated Early Development Services Team at PPD, responsible for conducting early phase studies with our network sites and phase I units.

You will be responsible for managing and maintaining relationships with early phase network sites.

You will be involved in the development of study specific plans; perform and coordinate all aspects of the clinical monitoring, site management oversight, support clinical management activities and interactions with sponsors.

Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation.

Manages procedures and guidelines from different sponsors and/or monitoring environments.

Acts as a site processes specialist, ensuring that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations and SOPs to guarantee subjects rights, well-being and data reliability.

Ensures audit readiness.

Develops collaborative relationships with investigational sites.

Detailed tasks and responsibilities assigned to role are outlined in the task matrix.



Essential Functions:

* Monitors investigator sites: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks.

Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site and remote monitoring activities.

Assess investigational product through physical inventory and records review.

Documents observations in reports and letters in a timely manner using approved business writing standards.

Escalates observed deficiencies and issues to project leads expeditiously and follow all issues through to resolution.

May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner.

Conducts monitoring tasks in accordance with the approved monitoring plan.

Participates in the investigator payment process.

Ensures a shared responsibility with other project team members on issues/findings resolution.

Investigates and follows-up on findings as applicable.



* Participates in investigator meetings as necessary.

Identifies potential investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites.

Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted.

Performs trial close out and retrieval of trial materials.



* Ensures that required essential documents are complete and in place, according to ICH-GCP and applicable regulations.

Conducts on-site file reviews as per project specifications.



* Provides trial status tracking and progress update reports to the Project lead and Client company as required.

Ensures study systems are updated per agreed study conventions (e.

g.

Clinical Trial Management System).



* Facilitates effective communication between investigative sites, the client company and the PPD project team through written, oral and/or electronic contacts.

* Responds to company, client and applicable regulatory requirements/audits/inspections.



* Maintains & completes administrative tasks such as expense reports and timesheets in a timely manner.

* Contributes to the project team by assisting in preparation of project publications/tools and sharing ideas/suggestions with team members.



* Contributes to other project work and initiatives for process improvement, as required.







Education and Experience:
Bachelor's degree in a life science related field or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification.



Previous experience as a CRA with 2 - 3 years experience that provides the knowledge, skills, and abilities to perform the job (comparable to 3 years as a clinical research monitor).



Valid driver's license where applicable.



In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills and Abilities:

* Effective clinical monitoring skills
* Excellent understanding and demonstrated application of FDA guidelines, ICH GCPs, applicable regulations and procedural documents
* Well-developed critical thinking skills, including but not limited to: critical mindset, in-depth investigation for appropriate root cause analysis and problem solving.


* Manages Risk Based Monitoring concepts and processes
* Ability to mentor and train other monitors in a positive and effective manner
* Ability to evaluate medical research data and proficient knowledge of medical terminology
* Effective oral and written communication skills, with the ability to communicate effectively with medical personnel
* Ability to maintain customer focus through the utilization of good listening skills, attention to detail and the ability to perceive customers’ underlying issues
* Excellent interpersonal skills
* Strong attention to detail Effective organizational and time management skills
* Ability to remain flexible and adaptable in a wide range of scenarios
* Excellent team player with team building skills
* Ability to work independently as required
* Ability to utilize problem-solving techniques applicable to constantly changing environment
* Good computer skills: proficient knowledge of Microsoft Office and the ability to learn appropriate software
* Good English language and grammar skills
* Effective presentation skills
Working Environment:
PPD values the health and wellbeing of our employees.

We support and encourage individuals to create a healthy and balanced environment where they can thrive.

Below is listed the working environment/requirements for this role:

Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.



Able to work upright and stationary for typical working hours.



Able to work in non-traditional work environments.



Able to use and learn standard office equipment and technology with proficiency.



Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.



May have exposure to potentially hazardous elements typically found in healthcare or laboratory environments.



This role requires independent travel up to 80%, inclusive of traveling in automobiles, airplanes, and trains.



PPD Defining Principles:
- We have a strong will to win - We earn our customer’s trust - We are game changers - We do the right thing - We are one PPD

If you resonate with our five principles above, and ultimately wish to accelerate the delivery of safe and effective therapeutics for some of the world’s most urgent health needs, then please submit your application – we’d love to hear from you.





**Job:** **Clinical Research Associates*

**Organization:** **NZ BU*


**Title:** *CRA/Sr CRA - Early Development Services*

**Location:** *NZ-NZ-Auckland-Auckland NZ Westhaven Drive*

**Requisition ID:** *223063*

PPD is an affirmative action employer that values diversity as a strength fosters and environment of mutual respect.

PPD provides equal employment opportunities without regard to age, race, color, pregnancy, national origin, religion, sex, gender identity, sexual orientation, disability, veteran status or other status within any other protected group

Required Skill Profession

Other General