Clinical Data Monitor II Information

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Covance Inc.

Covance, with headquarters in Princeton, New Jersey, is one of the world’s largest and most comprehensive drug development services companies, with annual revenues greater than $2 billion, employees in more than 60 countries, and more than 11,000 employees worldwide. NONCLINICAL DEVELOPMENT(Toxicology, Research Products, Analytical Services) * Managed 443 compound development programs (>250 IND/CTA enabling), with over 100 different sponsors, which led to 41 IND/CTA applications in 2... Read More

Address	210 Carnegie Ctr Princeton, NJ 08540 (609) 452-8550
Website	www.covance.com/
Holding	No Holding Details

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Clinical Data Monitor II

COVANCE is a market leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries.

At our central Leeds site, we conduct phase I and IIa clinical trials on healthy human volunteers at our state of the art 72 bed clinical ward. These trials play an essential role in developing a host of new medicines which improve the lives of millions.

We are currently recruiting for a Clinical Data Monitor II to join our Clinical Operations team. As a Clinical Data Monitor II, you will be involved in all aspects of the capture and review of data generated in studies performed at the Clinic. The duties and responsibilities may include:

• Review draft protocols, Case Report Form’s (CRFs), completed study CRFs paying particular attention to data capture issues and return/ supplying comments to the relevant people.
• Attend project Start Up Meetings, contributing to all data capture issues where appropriate.
• Assist with query solutions.
• Ongoing daily Quality Check of Study data.
• Liaise with the Clinical Data Monitor I regarding the schedule of data transfer into the Data Monitoring department.
• Review the completed study CRFs and release into the Data Management department.
• Schedule the signing of completed CRFs with the Principal or Associate Investigator.
• Organise and authorise the photocopying of completed CRFs. Despatch the completed CRFs to the Sponsor according to the agreed schedule.
• Review relevant Standard Operating Procedures (SOPs) and introduce new SOPs as appropriate.
• Attend process review meetings (as required) when the department is involved.

You will typically be educated to degree level or equivalent in a life science subject. You should ideally have recent relevant experience applicable to this role.

We Offer

Covance’s ongoing success offers team members unsurpassed growth and career development opportunities.

At Covance, we help make the miracles of medicine a reality. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career.

There is no better time to join us!
Education/Qualifications   Educated to A level standard or equivalent
Working knowledge of computers and programs (e.g., Word, Excel).
Requires unquestionable customer service skills and ability to be persistent while maintaining tact.
Requires great attention to detail.
Relevant Science Degree (eg Biochemistry, Pharmacology) or Medical Laboratory Scientific Officer or equivalent relevant experience.
Experience   Typically 2-3 years of applicable experience.
Knowledge of science or a scientific background is preferred.
Excellent written and oral communication skills.
Meticulous attention to detail
Ability to work to strict deadlines
Ability to remain calm under pressure
Good organizational skills
Ability to priorities
Negotiation skills
EEO Employer   Covance is committed to diversity in the workplace and is an equal opportunity employer. (M/F/D/V). Your confidentiality and privacy are important to us.

Other Job Information

Vacancy type:	Full Time	Contact Mode:	not provided
Fax:	+1-302-6555049	Contact Name:	not provided
Job Duration:	not provided	Phone:	+1-609-4524440
Email:	not provided