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Careers
Comac Medical is a Full Service CRO/SMO providing clinical research services across 30 countries. After more than 24 years on the field of clinical research we have a global presence. We take pride in our strong growth and solid reputation we’ve built within the drug development industry.
Overview

Our team‘s experience and expertise has distinguished Comac Medical which has become a leading CRO on the Balkan region. Our employees are remaining the most valuable asset. We recognize their essential contributions in building relationships with our clients and associates. We provide training and development to our staff needs’ to support them remain on top of their respective fields. We invest in employee professional development and personal growth, we reward their performance with compensation and benefits.

The Company Offers:
  • Work for successful and dynamic international company
  • Excellent internal training and career development opportunities in a perspective professional field
  • Stimulate and result orientated remuneration package

If you are interested apply on hr@comac-medical.com with your CV and cover letter describing why your experience and skills make you a good candidate for the position.

Recent Job Offers
Project leader

Great job opportunity for a CLINICAL REASRCH PROEJCT LEADER for one of the most reputable, full-service providers of CRO and SMO.

Established in 1997, with locations in Central & Eastern Europe and 290 full-time dedicated professionals, COMAC MEDICAL is a recognized leader in clinical research and provides innovative and non-conventional solutions of high quality for pharmaceutical industry.

Currently we are looking for a proven professional to obtain the role with a flying start and deep dive into the daily tasks with confidence and knowledge.

 

What is expected to be done?

 

  • Monitor and manage project milestones and timelines as per the contract obligations;
  • Determine project-specific oversight metrics, as needed, in agreement with the client;
  • Perform risk assessment and propose mitigation strategy for the project;
  • Prepare, oversee, and review documents related to assigned clinical research project;
  • Provide regular updates of project status to the client and operational team;
  • Ensure effective and proper communication between all parties involved in the project;
  • Coordinate and conduct internal kick-off meeting as well as of kick-off meeting with the client;
  • Organize and supervise of project-specific training;
  • Oversee and control all logistic procedures related to the study and serve as a signal point of contact for the management and client;
  • Fully involved in resolving project issues, as well as take part in procedure improvement initiatives;
  • Supervise of project submission/approval process to EC/RA
  • Support quality group in preparation of project-specific audit as needed
  • Translation of project-specific documents, when necessary
  • Participate in marketing activities, client presentations, and proposal development

 

What is required for the role?

 

  • Graduate or postgraduate degree, preferably in the filed of Biology, Pharmacy, Chemistry or other relevant;
  • Minimum 3 years of experience in the leading role in a clinical research filed;
  • Excellent knowledge of clinical research process;
  • Excellent knowledge of current ICH/GCP guidelines and country-specific regulations;
  • Exceptional problem-solving, organizational, and leadership skills;
  • Outstanding communication skills – able to successfully convey massages across both dedicated team and external teams involved in the clinical research;
  • Ability to keep deadlines for multiple projects in a demanding working environment;
  • Ability to pay attention to details, absorb and analyse specific project data;
  • Working knowledge of Word, Excel, and Power Point;
  • Fluency in English language;

 

 

Why to join Comac Medical?

 

  • Great team of knowledgeable, high-achieving and experienced professionals;
  • International and diverse work atmosphere;
  • Challenging projects in a different therapeutical area as well as in early phases;
  • Opportunity to enrich professional skills and progress in career development;
  • Work from home policy
  • Competitive remuneration;
  • Additional health insurance and food vouchers;
  • Professional trainings;

 

Core strengths of Comac Medical

 

  • Proven track record for quality and delivery;
  • Established and trusted relationships with KOLs;
  • Motivated, capable and dedicated team;
  • Global full-service capabilities;

 

If you are interested, challenged and convinced that the job opportunity is exactly for you, do not hesitate and send your detailed resume in English.

Only the shortlisted candidates will be contacted in a timely manner.

Data Manager - Bulgaria

Great job opportunity for a Data Manager for one of the most reputable, full-service providers of CRO and SMO.

Established in 1997, with locations in Central & Eastern Europe and 290 full-time dedicated professionals, COMAC MEDICAL is a recognized leader in clinical research and provides innovative and non-conventional solutions of high quality for pharmaceutical industry.

Currently, we are looking for an inspiring Leader to join our Data Management team of highly achieved and dedicate professionals.

 What is expected to be done?

  • Act as Lead Data Manager, coordinate data management team to successful completion of clinical trial projects within given timelines;
  • Interact with clients and project manager as main contact person
  • Prepare and review paper CRF, annotated CRF, EDC specification, Data Validation Specification, Data Management Plan
  • Set-up and validate the study-specific clinical database;
  • Develop CRF Completion Guidelines;
  • Supervise double data entry process;
  • Monitor coding and medical review processes related to clinical database
  • Prepare Data Transfer Agreements;
  • Perform QC of the database in case of double data entry;
  • Track and clean the data in the clinical database;
  • Prepare of study specific data management documents for trial master file;
  • Assist Quality Group in preparation of data management SOPs;
  • Support Quality Group in preparation of audit on the Data Management activities;

 

What is required for the role?

  • University degree in Mathematics, Computer Science or relevant fields;
  • At least 2 years of experience in Data Management in the clinical trial settings;
  • Thorough knowledge of current ICH/GCP guidelines and applicable regulations;
  • Strong working knowledge of SDTM, CDISC controlled terminology;
  • Experience with SAS and/or SQL;
  • Excellent analytical capabilities, inclination to non-standard problem solving;
  • Excellent organizational, communication and interpersonal skills;
  • Positive attitude and ability to interact with all levels of staff;
  • Proficiency in English;
  • Ability to keep and work with tight deadlines;

 

Why to join Comac Medical?

  • Great team of knowledgeable, high-achieving, and experienced professionals;
  • International and diverse work atmosphere;
  • Challenging projects in a different therapeutical area as well as in early phases;
  • Opportunity to enrich professional skills and progress in career development;
  • Work from home policy
  • Competitive salary and social benefits;

 

Core strengths of Comac Medical:

  • Dedicated state-of-art Phase I Unit;
  • Proven track record for quality and delivery;
  • Established and trusted relationships with KOLs;
  • Motivated, capable and dedicated team;
  • Global full-service capabilities;

 

 Do not ignore this opportunity! Check it out!

I will be glad to speak to you and give you more details about the company, projects, values, people etc

 

 

Clinical Research Associate - Croatia

Great job opportunity for a CLINICAL RESEARCH ASSOCIATE for one of the most reputable, full-service providers of CRO and SMO, COMAC MEDICAL,  with headquarter in Sofia, Bulgaria.

Established in 1997, with locations in Central & Eastern Europe and 290 full-time dedicated professionals, we are a recognized leader in clinical research and provides innovative and non-conventional solutions of high quality for pharmaceutical industry.

 

Currently we are looking for a professional to join our Croatian Team

What is expected to be done:

  • Conducts feasibility studies and site qualification visits;
  • Develops and ensures strong site relationship through all phases of the trial;
  • Gains in-depth understanding of the study protocol and related procedures;
  • Prepares study documentation e.g. draft protocols, draft CRFs;
  • Collects, reviews, and monitors required regulatory documentation;
  • Communicates with Investigators and site staff on issues related to protocols;
  • Conducts recruitment, retention, protocol deviations, regulatory documentation, site audits/inspections and overall site performance;
  • Performs remote and on-site monitoring & oversight activities;
  • Identifies, assesses and resolves site performance, quality or compliance problems
  • Escalates if necessary, by following CRA Escalation Pathway in collaboration with CTL/CMM/PL;
  • Assists in planning and execution of Investigator Meetings or other study related meetings;
  • Assume additional responsibilities as required by Project Manager;

What is required for the role?

  • Graduate or postgraduate degree, preferably in the filed of Biology, Pharmacy, Chemistry or other relevant;
  • At least 3 years of experience as a Clinical Research Associate/Clinical Monitor;
  • Excellent knowledge of clinical research process;
  • Good knowledge of all functional areas of clinical trial management;
  • Working knowledge of current ICH/GCP guidelines and applicable country-specific regulations;
  • Excellent organizational, communication (verbal and written)
  • Positive attitude and ability to interact with various levels of personnel
  • Good analytical and problem-solving skills;
  • Ability to travel for site monitoring and/or co-monitoring activities, attend investigator meetings or vendor visits/audits, as required (up to 30%)
  • Ability to keep tight deadlines and work in a dynamic environment;
  • Working knowledge of Word, Excel, and Power Point
  • Fluency in English language

Why to join Comac Medical?

  • Great team of knowledgeable, high-achieving and experienced professionals;
  • International and diverse work atmosphere;
  • Challenging projects in a different therapeutic area as well as in early phases;
  • Opportunity to enrich professional skills and progress in career development;
  • Competitive remuneration;
  • Professional trainings;

Core strengths of Comac Medical

  • Proven track record for quality and delivery;
  • Established and trusted relationships with KOLs;
  • Motivated, capable and dedicated team;
  • Global full-service capabilities;

If you are interested, challenged and convinced that the job opportunity is exactly for you, do not hesitate and send your detailed resume in English.

Only the shortlisted candidates will be contacted in a timely manner.

IT Service Desk and QA Specialist - Bulgaria

Great job opportunity for an IT Service Desk and QA Specialist in one of the most reputable, full-service providers of CRO and SMO

Established in 1997, with locations in Central & Eastern Europe and 290 full-time dedicated professionals, COMAC MEDICAL is a recognized leader in clinical research and provides innovative and non-conventional solutions of high quality for the pharmaceutical industry.

In this role, you will provide maintenance of the computer desktop environment by analyzing requirements, resolving problems, installing hardware and software solutions, and supporting the internal IT Help desk. You will be responsible for the administration and internal support of the Company’s PCs, printers, servers and related equipment. Tasks include end-user support, license tracking, and performing PC maintenance, upgrades and configurations.

 

What is expected to be done?

  • Provide helpdesk support and resolve problems to the end user’s satisfaction
  • Monitor and respond quickly and effectively to requests received through the IT help desk
  • Respond to queries either in person or over the phone and monitor pending support requests based on priority
  • Modify configurations, utilities, software default settings, etc. for the local workstation
  • Utilize and maintain the asset management
  • Assist with on-boarding of new users
  • Train computer users and write training manuals, if needed
  • Ensure each workstation is properly equipped
  • Install, test and configure new workstations, peripheral equipment and software
  • Maintain inventory of all equipment, software and software licenses
  • Report issues to the IT Manager
  • Assign users and computers to proper groups in Active Directory
  • Perform timely workstation hardware and software upgrades as required
  • Document internal and external procedures as well as some software systems
  • Collaborate with development team members regarding testing strategies, plans and scheduled releases
  • Support and help team members with automation QA tasks
  • Analyse, describe and track defects in a bug tracking system
  • Design, develop, maintain and improve test documentation
  • Contribute to adjust Test Automation to a Continuous Delivery Process

 

What is expected of the role?

  • University degree in IT specialty is preferable
  • Excellent command of spoken and written English
  • Previous experience in a similar position will be considered an advantage;
  • Advanced knowledge of Windows OS and Linux OS
  • Very good attention to detail, excellent analytical capabilities
  • Responsible, pro-active, well-organized, and committed person, team player
  • Ability to work under pressure and to keep tight deadlines
  • Knowledge and experience in test case design end execution
  • Experience with web applications manual and automation testing
  • Knowledge and experience with testing methodologies and techniques and QA processes

 

Why join Comac Medical?

  • Working for a successful international company, the opportunity for career development in a perspective professional field
  • Competitive remuneration
  • Friendly working environment
  • Additional benefits – food vouchers, additional health insurance

 

Core strengths of Comac Medical:

 

  • Dedicated state-of-art Phase I Unit
  • Proven track record for quality and delivery
  • Established and trusted relationships with KOLs
  • Motivated, capable and dedicated team
  • Global full-service capabilities

 

Do not ignore this opportunity! Check it out!

Only the short-listed candidates will be contacted in a timely manner.

Site Coordinator - Bulgaria

Great job opportunity for a SITE COORDINATOR for one of the most reputable, full-service providers of CRO and SMO

Established in 1997, with locations in Central & Eastern Europe and 290 full-time dedicated professionals, COMAC MEDICAL is a recognized leader in clinical research and provides innovative and non-conventional solutions of high quality for the pharmaceutical industry.

Currently, we are looking for a professional to work closely with the CLINICAL SITE MANAGER, to coordinate clinical research studies activities, to streamline processes, administration and communication between teams involved in the study.

 

What is expected to be done?

  • Support all types of feasibility inquiries at the respective site;
  • Assist the site team with regards to subject pre-selection and recruitment;
  • Help the site team in subjects’ visits planning and preparation;
  • Organize various source of documentation;
  • Complete Case Report Form and maintain Investigator Site File;
  • Participate and coordinate any trainings and meetings (incl. Investigator Meetings) related to a specific study;
  • Collaborate with the site team for any adverse events and safety information reporting and escalation;
  • Organize and coordinate logistic of study medication, other study supplies and biological samples;
  • Ensure timely site equipment maintenance and calibration;
  • Handle subject expenses reimbursement;
  • Support project team in the collection of site-specific documents;
  • Support the site team in audit/inspection preparation, as needed

What is required for the role?

  • Graduate or postgraduate degree, preferably in the filed of Biology, Pharmacy, Chemistry or other relevant;
  • One year of experience in the leading role in a clinical research filed;
  • Very good knowledge of clinical research process;
  • Sound knowledge of current ICH/GCP guidelines and country-specific regulations;
  • Particularly good organizational and coordination skills;
  • Excellent communication skills both written and spoken;
  • Working knowledge of Word, Excel, and Power Point;
  • Fluency in English language;

Why join Comac Medical?

  • Great team of knowledgeable, high-achieving and experienced professionals;
  • International and diverse work atmosphere;
  • Challenging projects in a different therapeutical area as well as in early phases;
  • Opportunity to enrich professional skills and progress in career development;
  • Competitive remuneration;
  • Additional health insurance and food vouchers;
  • Professional trainings;

Core strengths of Comac Medical

  • Proven track record for quality and delivery;
  • Established and trusted relationships with KOLs;
  • Motivated, capable and dedicated team;
  • Global full-service capabilities;

 

If you are interested, challenged, and convinced that the job opportunity is exactly for you, do not hesitate and send your detailed resume in English.

Only the shortlisted candidates will be contacted in a timely manner.

Clinical Trial Assistant - Bulgaria

Great job opportunity for a CLINICAL TRIAL ASSISTANT for one of the most reputable, full-service providers of CRO and SMO.

Established in 1997, with locations in Central & Eastern Europe and over, COMAC MEDICAL is a recognized leader in clinical research and provides innovative and non-conventional solutions of high quality for the pharmaceutical industry.

Currently, we are looking for a professional to work closely with our Project Leaders, coordinate clinical research project activities, and assist in streamlining processes and communication between parties involved.

 

What is expected to be done?

  • Support Project Leaders in the organization of project-specific training, аs directed
  • Support Project Leaders/Associate Project Leads in the creation and filing of project management documents
  • Support Project Leaders/Associate Project Leads in the organization of internal kick-off meetings as well as kick-off meetings with the client
  • Translation of project-specific documents, when necessary
  • Assume additional responsibilities as directed by Project Manager

What is required for the role?

  • Graduate or postgraduate degree
  • Working knowledge of current ICH/GCP guidelines and applicable country-specific regulations.
  • Proficiency in English
  • Ability to work under pressure and to keep tight deadlines
  • Working knowledge of Word, Excel, and Power Point.

Why join Comac Medical?

  • We are proud of our great team of knowledgeable, high-achieving, and experienced professionals
  • You will be a part of an International and diverse work environment
  • Be a part of challenging projects in a different therapeutic area as well as in early phases
  • We offer a competitive remuneration
  • You will receive and will participate in a number of training to enrich your professional knowledge

Core strengths of Comac Medical:

  • Proven track record for quality and delivery
  • Established and trusted relationships with KOLs
  • Motivated, capable and dedicated team
  • Global full-service capabilities

If you are interested, challenged and convinced that the job opportunity is exactly for you, do not hesitate and send your detailed resume in English.

Only the shortlisted candidates will be contacted in a timely manner.

Senior Project Manager - Romania

Join Comac Medical as a Senior Project Manager and play a pivotal role in advancing healthcare through innovative clinical research.

Key responsibilities:

Project Planning and Set Up:

  • Lead project initiation to closure, ensuring relevant information gathering.
  • Collaborate with internal teams for resource allocation and feasibility activities.
  • Create comprehensive project management plans, oversee submission processes, and organize kick-off meetings.
  • Act as a single point of contact with clients and mentor team members.

Project Execution and Control:

  • Track and control project milestones, ensuring consistent organization and execution.
  • Provide regular updates to clients and operational teams.
  • Manage project-specific training, issue resolution, and logistic procedures.

Business Development:

  • Participate in marketing activities, client presentations, and proposal development.
  • Represent Comac Medical in professional and industry meetings.

Qualifications:

  • Graduate or postgraduate in relevant field.
  • Minimum 4 years of clinical trial management experience.
  • Proficiency in English.
  • Thorough knowledge of clinical research processes, ICH/GCP guidelines, and country-specific regulations.
  • Strong organizational, communication, and leadership skills.
  • Ability to work under pressure and meet tight deadlines.
  • Computer literacy, including MS Office and e-Clinical systems.

 

Apply now and contribute to the success of groundbreaking clinical trials with Comac Medical!

 

 

Clinical Research Associate - Lithuania

As a Clinical Research Associate you will:

  • Conduct feasibility studies and site qualification visits
  • Develop and maintain strong relationships with sites throughout the trial phases
  • Gain an in-depth understanding of study protocols and related procedures
  • Prepare study documentation, including draft protocols and CRFs
  • Collect, review, and monitor required regulatory documentation
  • Communicate effectively with Investigators and site staff regarding protocol-related issues
  • Perform recruitment, retention, protocol deviation, regulatory documentation, and site audits/inspections
  • Engage in remote and on-site monitoring and oversight activities
  • Identify, assess, and resolve site performance, quality, or compliance issues
  • Collaborate with CTL/CMM/PL to escalate issues if necessary, following the CRA Escalation Pathway
  • Assist in planning and executing Investigator Meetings or other study-related meetings
  • Assume additional responsibilities as required by the Project Manager

 

Qualifications for the role:

  • Graduate or postgraduate degree, preferably in Biology, Pharmacy, Chemistry, or a related field
  • Minimum of 3 years of experience as a Clinical Research Associate/Clinical Monitor
  • Excellent knowledge of the clinical research process
  • Good understanding of all functional areas of clinical trial management
  • Working knowledge of current ICH/GCP guidelines and applicable country-specific regulations
  • Excellent organizational and communication skills (verbal and written)
  • Positive attitude with the ability to interact with personnel at various levels
  • Strong analytical and problem-solving skills
  • Willingness to travel for site monitoring and/or co-monitoring activities, attend investigator meetings, or vendor visits/audits (up to 30%)
  • Ability to meet tight deadlines and work in a dynamic environment
  • Proficiency in Word, Excel, and PowerPoint
  • Fluency in English

 

Why join COMAC MEDICAL?

  • Join a team of knowledgeable, high-achieving, and experienced professionals
  • Experience an international and diverse work atmosphere
  • Take on challenging projects in various therapeutic areas, including early phases
  • Enhance your professional skills and progress in your career development
  • Enjoy competitive remuneration and access to professional trainings

 

If you are interested, challenged, and convinced that this job opportunity is the right fit for you, don’t hesitate to send your detailed resume in English.

Please note that only shortlisted candidates will be contacted in a timely manner.

 

Senior Project Manager - Poland

Join Comac Medical as a Senior Project Manager and play a pivotal role in advancing healthcare through innovative clinical research.

Key responsibilities:

Project Planning and Set Up:

  • Lead project initiation to closure, ensuring relevant information gathering.
  • Collaborate with internal teams for resource allocation and feasibility activities.
  • Create comprehensive project management plans, oversee submission processes, and organize kick-off meetings.
  • Act as a single point of contact with clients and mentor team members.

Project Execution and Control:

  • Track and control project milestones, ensuring consistent organization and execution.
  • Provide regular updates to clients and operational teams.
  • Manage project-specific training, issue resolution, and logistic procedures.

Business Development:

  • Participate in marketing activities, client presentations, and proposal development.
  • Represent Comac Medical in professional and industry meetings.

Qualifications:

  • Graduate or postgraduate in relevant field.
  • Minimum 4 years of clinical trial management experience.
  • Proficiency in English.
  • Thorough knowledge of clinical research processes, ICH/GCP guidelines, and country-specific regulations.
  • Strong organizational, communication, and leadership skills.
  • Ability to work under pressure and meet tight deadlines.
  • Computer literacy, including MS Office and e-Clinical systems.

 

Apply now and contribute to the success of groundbreaking clinical trials with Comac Medical!

Clinical Research Associate - Poland

As a Clinical Research Associate you will:

  • Conduct feasibility studies and site qualification visits
  • Develop and maintain strong relationships with sites throughout the trial phases
  • Gain an in-depth understanding of study protocols and related procedures
  • Prepare study documentation, including draft protocols and CRFs
  • Collect, review, and monitor required regulatory documentation
  • Communicate effectively with Investigators and site staff regarding protocol-related issues
  • Perform recruitment, retention, protocol deviation, regulatory documentation, and site audits/inspections
  • Engage in remote and on-site monitoring and oversight activities
  • Identify, assess, and resolve site performance, quality, or compliance issues
  • Collaborate with CTL/CMM/PL to escalate issues if necessary, following the CRA Escalation Pathway
  • Assist in planning and executing Investigator Meetings or other study-related meetings
  • Assume additional responsibilities as required by the Project Manager

 

Qualifications for the role:

  • Graduate or postgraduate degree, preferably in Biology, Pharmacy, Chemistry, or a related field
  • Minimum of 3 years of experience as a Clinical Research Associate/Clinical Monitor
  • Excellent knowledge of the clinical research process
  • Good understanding of all functional areas of clinical trial management
  • Working knowledge of current ICH/GCP guidelines and applicable country-specific regulations
  • Excellent organizational and communication skills (verbal and written)
  • Positive attitude with the ability to interact with personnel at various levels
  • Strong analytical and problem-solving skills
  • Willingness to travel for site monitoring and/or co-monitoring activities, attend investigator meetings, or vendor visits/audits (up to 30%)
  • Ability to meet tight deadlines and work in a dynamic environment
  • Proficiency in Word, Excel, and PowerPoint
  • Fluency in English

 

Why join COMAC MEDICAL?

  • Join a team of knowledgeable, high-achieving, and experienced professionals
  • Experience an international and diverse work atmosphere
  • Take on challenging projects in various therapeutic areas, including early phases
  • Enhance your professional skills and progress in your career development
  • Enjoy competitive remuneration and access to professional trainings

 

If you are interested, challenged, and convinced that this job opportunity is the right fit for you, don’t hesitate to send your detailed resume in English.

Please note that only shortlisted candidates will be contacted in a timely manner.

 

SUBMIT RFP